| geneid | 55013 |
|---|---|
| ensemblid | ENSG00000005059.16 |
| hgncid | 26076 |
| symbol | MCUB |
| name | mitochondrial calcium uniporter dominant negative subunit beta |
| refseq_nuc | NM_017918.5 |
| refseq_prot | NP_060388.2 |
| ensembl_nuc | ENST00000394650.7 |
| ensembl_prot | ENSP00000378145.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 109560246 |
| end | 109688719 |
| strand | + |
| ver | v1.2 |
| region | chr4:109560246-109688719 |
| region5000 | chr4:109555246-109693719 |
| regionname0 | MCUB_chr4_109560246_109688719 |
| regionname5000 | MCUB_chr4_109555246_109693719 |
| 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 | 1/0 | 336 | 152 | 56 | 19 | 53 | 7 | 16 | 42 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0002 | 0/0 | 336 | 87 | 12 | 22 | 46 | 2 | 5 | 34 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0003 | 0/1 | 336 | 78 | 7 | 17 | 35 | 3 | 15 | 27 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0004 | 0/0 | 336 | 16 | 14 | 2 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0005 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0006 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0007 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| 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 | 1011 | 140 | 52 | 17 | 49 | 7 | 15 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0002 | 0/0 | 1011 | 86 | 11 | 22 | 46 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0003 | 0/1 | 1011 | 75 | 7 | 17 | 32 | 3 | 15 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0004 | 0/0 | 1011 | 16 | 14 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0005 | 1/0 | 1011 | 7 | 4 | 1 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0006 | 0/0 | 1011 | 4 | 0 | 0 | 4 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0007 | 0/0 | 1011 | 3 | 0 | 0 | 3 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0008 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0009 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0010 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0011 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| c0012 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1220 | 169 | 56 | 29 | 59 | 4 | 20 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0002 | 1/0 | 1220 | 92 | 16 | 22 | 45 | 2 | 6 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0003 | 0/0 | 1220 | 34 | 3 | 6 | 19 | 4 | 2 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0004 | 0/0 | 1220 | 17 | 10 | 0 | 0 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0005 | 0/0 | 1220 | 14 | 0 | 0 | 11 | 0 | 3 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0006 | 0/0 | 1223 | 5 | 4 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0007 | 0/0 | 1220 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0008 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0009 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| t0010 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| 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 | 2 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| 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 | 1011 | 140 | 52 | 17 | 49 | 7 | 15 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0005 | 1/0 | 1011 | 7 | 4 | 1 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0006 | 0/0 | 1011 | 4 | 0 | 0 | 4 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0012 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0002c0002 | 0/0 | 1011 | 86 | 11 | 22 | 46 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0002c0011 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0003c0003 | 0/1 | 1011 | 75 | 7 | 17 | 32 | 3 | 15 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0003c0007 | 0/0 | 1011 | 3 | 0 | 0 | 3 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0004c0004 | 0/0 | 1011 | 16 | 14 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0005c0009 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0006c0008 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0007c0010 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2230 | 74 | 34 | 11 | 23 | 1 | 5 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0001t0002 | 0/0 | 2230 | 4 | 4 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0001t0003 | 0/0 | 2230 | 33 | 3 | 6 | 18 | 4 | 2 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0001t0004 | 0/0 | 2230 | 17 | 10 | 0 | 0 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0001t0005 | 0/0 | 2230 | 10 | 0 | 0 | 7 | 0 | 3 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0001t0008 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0001t0009 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0005t0002 | 1/0 | 2230 | 2 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0005t0006 | 0/0 | 2233 | 5 | 4 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0006t0005 | 0/0 | 2230 | 4 | 0 | 0 | 4 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0001c0012t0001 | 0/0 | 2230 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0002c0002t0002 | 0/0 | 2230 | 85 | 11 | 22 | 45 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0002c0002t0010 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0002c0011t0002 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0003c0003t0001 | 0/1 | 2230 | 73 | 7 | 15 | 32 | 3 | 15 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0003c0003t0007 | 0/0 | 2230 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0003c0007t0001 | 0/0 | 2230 | 3 | 0 | 0 | 3 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0004c0004t0001 | 0/0 | 2230 | 16 | 14 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0005c0009t0001 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0006c0008t0003 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| a0007c0010t0001 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | copy fasta | chr4 | 109555246 | 109693719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0002g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0006t0005g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0006t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0006t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0012t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0011t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0007g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0007t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0007t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0005c0009t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0006c0008t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0007c0010t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0233 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0317 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0146 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0267 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0297 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0167 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0227 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0219 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0223 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0240 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00735 | hp2 | a0004 | c0004 | t0001 | g0331 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0177 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00738 | hp2 | a0001 | c0005 | t0006 | g0326 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0162 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0266 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0147 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0276 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0121 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01109 | hp2 | a0004 | c0004 | t0001 | g0028 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0330 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0313 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0263 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01255 | hp1 | a0001 | c0012 | t0001 | g0051 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01255 | hp2 | a0003 | c0003 | t0007 | g0005 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0261 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0268 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01358 | hp2 | a0003 | c0003 | t0007 | g0005 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0238 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0043 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0321 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0234 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0277 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0289 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0175 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0204 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0235 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0245 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0212 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0053 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0161 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0273 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0124 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0254 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0143 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02015 | hp2 | a0001 | c0001 | t0008 | g0200 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0164 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02080 | hp1 | a0003 | c0003 | t0001 | g0294 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0259 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0302 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02135 | hp1 | a0007 | c0010 | t0001 | g0241 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0201 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02145 | hp1 | a0004 | c0004 | t0001 | g0284 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02145 | hp2 | a0004 | c0004 | t0001 | g0078 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0275 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02155 | hp2 | a0003 | c0007 | t0001 | g0308 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0270 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02257 | hp2 | a0005 | c0009 | t0001 | g0226 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0091 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0030 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0115 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0119 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0047 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0315 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0155 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02723 | hp1 | a0001 | c0005 | t0006 | g0008 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0097 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0296 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02809 | hp2 | a0001 | c0005 | t0006 | g0169 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02922 | hp1 | a0004 | c0004 | t0001 | g0037 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0033 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0228 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0156 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0108 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03017 | hp1 | a0001 | c0005 | t0002 | g0253 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0255 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03098 | hp2 | a0002 | c0011 | t0002 | g0050 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0054 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0013 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03195 | hp1 | a0001 | c0005 | t0006 | g0046 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03225 | hp1 | a0004 | c0004 | t0001 | g0065 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03453 | hp1 | a0004 | c0004 | t0001 | g0251 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0310 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0260 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0057 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03540 | hp2 | a0004 | c0004 | t0001 | g0034 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0320 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0316 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0158 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0099 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03704 | hp2 | a0003 | c0003 | t0001 | g0312 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0154 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0107 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0113 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0058 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0281 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0114 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0274 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0093 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0287 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0314 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | CHB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0318 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0246 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18947 | hp1 | a0006 | c0008 | t0003 | g0328 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18949 | hp2 | a0003 | c0007 | t0001 | g0102 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18964 | hp1 | a0001 | c0006 | t0005 | g0128 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0258 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18970 | hp1 | a0001 | c0006 | t0005 | g0002 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0257 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18975 | hp1 | a0003 | c0003 | t0001 | g0305 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0230 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0319 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19043 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0073 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19058 | hp1 | a0001 | c0006 | t0005 | g0136 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0282 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0244 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19079 | hp2 | a0001 | c0006 | t0005 | g0002 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19082 | hp1 | a0003 | c0007 | t0001 | g0269 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0262 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19090 | hp2 | a0002 | c0002 | t0010 | g0237 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0285 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19240 | hp1 | a0004 | c0004 | t0001 | g0252 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ASW | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ASW | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0120 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02486 | hp2 | a0004 | c0004 | t0001 | g0070 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | USA | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA21309 | hp2 | a0001 | c0005 | t0006 | g0009 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0272 | REF | REF | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0002 | g0247 | REF | REF | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109660207
|
T | A | 1 | a0002 | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
missense_variant | MODERATE | c.188T>A | p.Ile63Asn | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/8 | 280/2230 | 188/1011 | 63/336 | chr4 | 109660207 | ||
| chr4:109682677
|
A | C | 1 | a0007 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.547A>C | p.Lys183Gln | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/8 | 639/2230 | 547/1011 | 183/336 | chr4 | 109682677 | ||
| chr4:109684468
|
C | T | 1 | a0005 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.638C>T | p.Ser213Leu | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 730/2230 | 638/1011 | 213/336 | chr4 | 109684468 | ||
| chr4:109684588
|
A | T | 2 | a0003a0007 | 79 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
missense_variant | MODERATE | c.758A>T | p.Tyr253Phe | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 850/2230 | 758/1011 | 253/336 | chr4 | 109684588 | ||
| chr4:109684593
|
A | G | 1 | a0004 | 16 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(13): Show |
missense_variant | MODERATE | c.763A>G | p.Ile255Val | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 855/2230 | 763/1011 | 255/336 | chr4 | 109684593 | ||
| chr4:109684642
|
G | A | 1 | a0006 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.812G>A | p.Arg271Gln | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 904/2230 | 812/1011 | 271/336 | chr4 | 109684642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109560361
|
G | T | 2 | a0001c0012a0002c0011 | 2 | HG01255.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.24G>T | p.Pro8Pro | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/8 | 116/2230 | 24/1011 | 8/336 | chr4 | 109560361 | ||
| chr4:109682628
|
T | C | 9 | a0001c0001a0001c0006a0001c0012others(6): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
synonymous_variant | LOW | c.498T>C | p.Ser166Ser | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/8 | 590/2230 | 498/1011 | 166/336 | chr4 | 109682628 | ||
| chr4:109682736
|
T | A | 1 | a0001c0006 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
synonymous_variant | LOW | c.606T>A | p.Leu202Leu | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/8 | 698/2230 | 606/1011 | 202/336 | chr4 | 109682736 | ||
| chr4:109684625
|
A | G | 1 | a0003c0007 | 3 | HG02155.hp2 NA18949.hp2 NA19082.hp1 |
synonymous_variant | LOW | c.795A>G | p.Ala265Ala | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 887/2230 | 795/1011 | 265/336 | chr4 | 109684625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109560252
|
C | T | 1 | a0003c0003t0007 | 2 | HG01255.hp2 HG01358.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/8 | chr4 | 109560252 | ||||||
| chr4:109687811
|
G | A | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(11): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*219G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 219 | chr4 | 109687811 | |||||
| chr4:109687952
|
G | T | 1 | a0001c0001t0009 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 360 | chr4 | 109687952 | |||||
| chr4:109688106
|
A | G | 1 | a0002c0002t0010 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*514A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 514 | chr4 | 109688106 | |||||
| chr4:109688325
|
G | A | 2 | a0001c0001t0003a0006c0008t0003 | 34 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*733G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 733 | chr4 | 109688325 | |||||
| chr4:109688337
|
C | CTGA | 1 | a0001c0005t0006 | 5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*749_*751dupTGA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 752 | INFO_REALIGN_3_PRIME | chr4 | 109688337 | ||||
| chr4:109688458
|
A | G | 1 | a0001c0001t0008 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*866A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 866 | chr4 | 109688458 | |||||
| chr4:109688635
|
C | T | 12 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*1043C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 1043 | chr4 | 109688635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109560541
|
C | T | 1 | a0004c0004t0001g0331 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+105C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560541 | ||||||
| chr4:109560651
|
G | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+215G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560651 | ||||||
| chr4:109560711
|
G | T | 1 | a0002c0002t0002g0330 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.99+275G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560711 | ||||||
| chr4:109560738
|
G | A | 1 | a0002c0002t0002g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.99+302G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560738 | ||||||
| chr4:109560744
|
T | G | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+308T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560744 | ||||||
| chr4:109560887
|
C | A | 32 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+451C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560887 | ||||||
| chr4:109560889
|
C | A | 1 | a0002c0002t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99+453C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560889 | ||||||
| chr4:109560910
|
G | A | 2 | a0001c0001t0003g0011a0002c0002t0002g0010 | 2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99+474G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560910 | ||||||
| chr4:109560947
|
C | T | 2 | a0001c0001t0003g0329a0006c0008t0003g0328 | 2 | NA18947.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.99+511C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560947 | ||||||
| chr4:109560988
|
C | T | 2 | a0001c0001t0002g0327a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99+552C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560988 | ||||||
| chr4:109561073
|
T | TGGA | 98 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+642_99+644dupGA others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561073 | |||||
| chr4:109561421
|
T | C | 1 | a0001c0001t0003g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.99+985T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561421 | ||||||
| chr4:109561445
|
A | AT | 21 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0325others(18): Show | 21 | HG01884.hp1 HG02004.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+1018dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561445 | |||||
| chr4:109561445
|
A | ATT | 8 | a0001c0001t0004g0093a0001c0001t0005g0095a0001c0001t0005g0097others(5): Show | 8 | HG00621.hp2 HG02523.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1017_99+1018dup others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561445 | |||||
| chr4:109561445
|
AT | A | 37 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(34): Show | 37 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.99+1018delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561445 | |||||
| chr4:109561705
|
A | G | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1269A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561705 | ||||||
| chr4:109561830
|
C | G | 1 | a0002c0002t0002g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99+1394C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561830 | ||||||
| chr4:109561835
|
G | T | 10 | a0001c0001t0003g0069a0001c0001t0004g0093a0001c0001t0005g0095others(7): Show | 10 | HG00621.hp2 HG02040.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+1399G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561835 | ||||||
| chr4:109561952
|
T | A | 1 | a0003c0007t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.99+1516T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561952 | ||||||
| chr4:109562211
|
T | G | 2 | a0001c0001t0002g0044a0001c0001t0004g0045 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.99+1775T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562211 | ||||||
| chr4:109562285
|
C | A | 1 | a0002c0002t0002g0103 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.99+1849C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562285 | ||||||
| chr4:109562413
|
C | T | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+1977C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562413 | ||||||
| chr4:109562420
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.99+1984C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562420 | ||||||
| chr4:109562534
|
A | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 91 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+2098A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562534 | ||||||
| chr4:109562708
|
T | G | 2 | a0002c0002t0002g0012a0004c0004t0001g0013 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.99+2272T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562708 | ||||||
| chr4:109562709
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+2273G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562709 | ||||||
| chr4:109562881
|
G | GAA | 9 | a0001c0001t0002g0044a0001c0001t0004g0045a0001c0001t0004g0055others(6): Show | 9 | HG01975.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+2453_99+2454dup others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109562881 | |||||
| chr4:109562891
|
CAGTT | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0002g0067 | 3 | HG02647.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.99+2456_99+2459del others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562891 | ||||||
| chr4:109562949
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99+2513G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562949 | ||||||
| chr4:109563036
|
T | C | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2600T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563036 | ||||||
| chr4:109563187
|
T | C | 29 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0003g0069others(26): Show | 29 | HG00621.hp2 HG01884.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+2751T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563187 | ||||||
| chr4:109563233
|
C | A | 5 | a0001c0001t0002g0327a0001c0005t0006g0008a0001c0005t0006g0009others(2): Show | 5 | HG00738.hp2 HG01496.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2797C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563233 | ||||||
| chr4:109563242
|
G | A | 1 | a0001c0005t0006g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+2806G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563242 | ||||||
| chr4:109563268
|
T | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+2832T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563268 | ||||||
| chr4:109563275
|
A | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+2839A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563275 | ||||||
| chr4:109563402
|
T | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0105 | 3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+2966T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563402 | ||||||
| chr4:109563471
|
G | A | 1 | a0001c0005t0006g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+3035G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563471 | ||||||
| chr4:109563799
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.99+3363C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563799 | ||||||
| chr4:109563802
|
C | G | 3 | a0001c0001t0001g0323a0002c0002t0002g0007a0002c0002t0002g0322 | 3 | HG02132.hp2 HG02155.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.99+3366C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563802 | ||||||
| chr4:109563867
|
G | A | 32 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+3431G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563867 | ||||||
| chr4:109563879
|
G | A | 1 | a0003c0003t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+3443G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563879 | ||||||
| chr4:109563892
|
C | T | 1 | a0003c0003t0001g0321 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.99+3456C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563892 | ||||||
| chr4:109563956
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0009g0108 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.99+3520T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563956 | ||||||
| chr4:109564004
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.99+3568C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564004 | ||||||
| chr4:109564091
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+3655G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564091 | ||||||
| chr4:109564141
|
C | CT | 7 | a0001c0001t0001g0068a0001c0001t0001g0071a0002c0002t0002g0072others(4): Show | 7 | HG02647.hp2 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+3715dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109564141 | |||||
| chr4:109564219
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3783G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564219 | ||||||
| chr4:109564333
|
T | G | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+3897T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564333 | ||||||
| chr4:109564434
|
G | A | 2 | a0001c0001t0002g0327a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99+3998G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564434 | ||||||
| chr4:109564442
|
A | G | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99+4006A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564442 | ||||||
| chr4:109564469
|
C | T | 29 | a0001c0001t0001g0082a0001c0001t0002g0067a0001c0001t0003g0069others(26): Show | 29 | HG00621.hp2 HG01884.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+4033C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564469 | ||||||
| chr4:109564566
|
G | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(226): Show | 231 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.99+4130G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564566 | ||||||
| chr4:109564627
|
G | A | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4191G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564627 | ||||||
| chr4:109564976
|
C | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+4540C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564976 | ||||||
| chr4:109565132
|
G | A | 2 | a0002c0002t0002g0109a0002c0002t0002g0110 | 2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.99+4696G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565132 | ||||||
| chr4:109565157
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.99+4721T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565157 | ||||||
| chr4:109565336
|
A | C | 105 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(102): Show | 105 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.99+4900A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565336 | ||||||
| chr4:109565363
|
T | C | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4927T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565363 | ||||||
| chr4:109565389
|
A | G | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+4953A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565389 | ||||||
| chr4:109565503
|
G | A | 20 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0002g0067others(17): Show | 20 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+5067G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565503 | ||||||
| chr4:109565649
|
A | G | 1 | a0003c0003t0001g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.99+5213A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565649 | ||||||
| chr4:109565654
|
C | T | 2 | a0003c0003t0001g0318a0003c0003t0001g0319 | 2 | NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.99+5218C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565654 | ||||||
| chr4:109565838
|
CT | C | 55 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(52): Show | 55 | HG00323.hp2 HG00639.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.99+5419delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109565838 | |||||
| chr4:109565838
|
CTT | C | 44 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0023others(41): Show | 44 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.99+5418_99+5419del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109565838 | |||||
| chr4:109565872
|
C | T | 19 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0003g0076others(16): Show | 19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+5436C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565872 | ||||||
| chr4:109565927
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.99+5491T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565927 | ||||||
| chr4:109566023
|
G | T | 1 | a0001c0001t0003g0317 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99+5587G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566023 | ||||||
| chr4:109566048
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+5612G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566048 | ||||||
| chr4:109566192
|
G | T | 5 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0003g0101others(2): Show | 5 | HG00423.hp1 NA18994.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5756G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566192 | ||||||
| chr4:109566221
|
G | A | 1 | a0002c0002t0002g0112 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.99+5785G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566221 | ||||||
| chr4:109566251
|
C | T | 3 | a0001c0005t0006g0008a0001c0005t0006g0009a0003c0003t0001g0043 | 3 | HG01496.hp2 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+5815C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566251 | ||||||
| chr4:109566265
|
C | T | 2 | a0001c0001t0003g0217a0003c0003t0001g0216 | 2 | NA18983.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.99+5829C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566265 | ||||||
| chr4:109566266
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.99+5830G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566266 | ||||||
| chr4:109566271
|
T | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0044others(15): Show | 18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+5835T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566271 | ||||||
| chr4:109566343
|
G | A | 1 | a0001c0001t0005g0222 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.99+5907G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566343 | ||||||
| chr4:109566395
|
G | T | 3 | a0003c0003t0001g0314a0003c0003t0001g0315a0003c0003t0001g0316 | 3 | HG02698.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.99+5959G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566395 | ||||||
| chr4:109566422
|
A | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(23): Show | 26 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+5986A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566422 | ||||||
| chr4:109566445
|
A | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+6009A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566445 | ||||||
| chr4:109566456
|
T | C | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+6020T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566456 | ||||||
| chr4:109566469
|
CAA | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(50): Show | 53 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+6045_99+6046del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109566469 | |||||
| chr4:109566469
|
CAAA | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0044others(15): Show | 18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+6044_99+6046del others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109566469 | |||||
| chr4:109566479
|
A | T | 29 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0052others(26): Show | 29 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+6043A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566479 | ||||||
| chr4:109566481
|
AAT | A | 7 | a0001c0001t0001g0071a0001c0001t0004g0093a0001c0012t0001g0051others(4): Show | 7 | HG01255.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+6047_99+6048del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109566481 | |||||
| chr4:109566483
|
T | A | 4 | a0001c0001t0003g0232a0002c0002t0002g0233a0003c0003t0001g0234others(1): Show | 4 | HG00099.hp1 HG01517.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6047T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566483 | ||||||
| chr4:109566610
|
G | C | 1 | a0002c0002t0002g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99+6174G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566610 | ||||||
| chr4:109566819
|
T | C | 1 | a0002c0002t0002g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.99+6383T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566819 | ||||||
| chr4:109566864
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.99+6428G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566864 | ||||||
| chr4:109566895
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0044others(15): Show | 18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+6459A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566895 | ||||||
| chr4:109566917
|
C | T | 1 | a0002c0002t0002g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+6481C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566917 | ||||||
| chr4:109566920
|
G | A | 5 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0236others(2): Show | 6 | HG00140.hp1 HG00323.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+6484G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566920 | ||||||
| chr4:109566990
|
A | G | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+6554A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566990 | ||||||
| chr4:109567131
|
C | CA | 76 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(73): Show | 76 | HG00438.hp2 HG00639.hp1 HG01175.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+6717dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109567131 | |||||
| chr4:109567131
|
C | CAA | 12 | a0001c0001t0001g0026a0001c0001t0001g0052a0001c0001t0003g0076others(9): Show | 12 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6716_99+6717dup others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109567131 | |||||
| chr4:109567131
|
CA | C | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG01168.hp1 HG01168.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+6717delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109567131 | |||||
| chr4:109567237
|
A | G | 2 | a0002c0002t0002g0311a0003c0003t0007g0005 | 3 | HG01255.hp2 HG01358.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.99+6801A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567237 | ||||||
| chr4:109567275
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0044others(11): Show | 14 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+6839G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567275 | ||||||
| chr4:109567408
|
G | A | 5 | a0001c0001t0003g0122a0001c0001t0003g0123a0002c0002t0002g0120others(2): Show | 5 | HG01081.hp2 HG01109.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6972G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567408 | ||||||
| chr4:109567485
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.99+7049A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567485 | ||||||
| chr4:109567492
|
A | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0044others(15): Show | 18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+7056A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567492 | ||||||
| chr4:109567564
|
C | G | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+7128C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567564 | ||||||
| chr4:109567665
|
C | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(23): Show | 26 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+7229C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567665 | ||||||
| chr4:109567768
|
A | G | 1 | a0003c0003t0001g0310 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.99+7332A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567768 | ||||||
| chr4:109567882
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0002g0327others(1): Show | 4 | HG00738.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7446A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567882 | ||||||
| chr4:109567988
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99+7552C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567988 | ||||||
| chr4:109568077
|
G | GA | 26 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.99+7641_99+7642ins others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568077 | ||||||
| chr4:109568078
|
G | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.99+7642G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568078 | ||||||
| chr4:109568097
|
T | C | 26 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(23): Show | 26 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+7661T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568097 | ||||||
| chr4:109568112
|
C | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(25): Show | 28 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+7676C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568112 | ||||||
| chr4:109568356
|
C | T | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+7920C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568356 | ||||||
| chr4:109568423
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0040others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7987G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568423 | ||||||
| chr4:109568506
|
G | A | 19 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0003g0076others(16): Show | 19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+8070G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568506 | ||||||
| chr4:109568579
|
A | G | 2 | a0003c0003t0001g0315a0003c0003t0001g0316 | 2 | HG02698.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.99+8143A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568579 | ||||||
| chr4:109568609
|
T | G | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+8173T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568609 | ||||||
| chr4:109568621
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+8185G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568621 | ||||||
| chr4:109568676
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0002g0044others(15): Show | 18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+8240C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568676 | ||||||
| chr4:109568910
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+8474G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568910 | ||||||
| chr4:109568957
|
C | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+8521C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568957 | ||||||
| chr4:109568967
|
T | G | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+8531T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568967 | ||||||
| chr4:109569172
|
G | A | 1 | a0002c0002t0002g0322 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.99+8736G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569172 | ||||||
| chr4:109569191
|
T | C | 1 | a0002c0002t0002g0125 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99+8755T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569191 | ||||||
| chr4:109569196
|
G | GA | 19 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0003g0076others(16): Show | 19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+8760_99+8761ins others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569196 | ||||||
| chr4:109569207
|
C | T | 2 | a0001c0012t0001g0051a0002c0011t0002g0050 | 2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+8771C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569207 | ||||||
| chr4:109569326
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+8890G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569326 | ||||||
| chr4:109569466
|
G | A | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+9030G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569466 | ||||||
| chr4:109569496
|
CCTT | C | 3 | a0001c0005t0006g0008a0001c0005t0006g0009a0003c0003t0001g0043 | 3 | HG01496.hp2 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+9061_99+9063del others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569496 | ||||||
| chr4:109569497
|
C | CT | 38 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0207others(35): Show | 38 | HG01884.hp1 HG01934.hp1 HG02004.hp2 others(35): Show |
intron_variant | MODIFIER | c.99+9085dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109569497 | |||||
| chr4:109569497
|
CT | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(54): Show | 57 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.99+9085delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109569497 | |||||
| chr4:109569497
|
CTT | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0052others(24): Show | 27 | HG01975.hp2 HG02280.hp2 HG02622.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+9084_99+9085del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109569497 | |||||
| chr4:109569535
|
A | T | 2 | a0001c0001t0003g0077a0003c0003t0001g0084 | 2 | NA18973.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.99+9099A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569535 | ||||||
| chr4:109569596
|
C | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9160C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569596 | ||||||
| chr4:109569676
|
G | A | 3 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133 | 3 | NA18963.hp2 NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.99+9240G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569676 | ||||||
| chr4:109569683
|
A | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9247A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569683 | ||||||
| chr4:109569766
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0105 | 3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+9330G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569766 | ||||||
| chr4:109569792
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+9356C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569792 | ||||||
| chr4:109569883
|
A | C | 1 | a0003c0003t0001g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.99+9447A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569883 | ||||||
| chr4:109569944
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.99+9508G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569944 | ||||||
| chr4:109570107
|
C | T | 12 | a0001c0001t0001g0224a0001c0001t0003g0069a0001c0001t0004g0093others(9): Show | 12 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+9671C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570107 | ||||||
| chr4:109570133
|
T | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9697T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570133 | ||||||
| chr4:109570283
|
G | A | 1 | a0001c0005t0006g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+9847G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570283 | ||||||
| chr4:109570312
|
G | T | 3 | a0001c0001t0003g0076a0002c0002t0002g0075a0002c0002t0002g0083 | 3 | HG02071.hp1 HG02080.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.99+9876G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570312 | ||||||
| chr4:109570341
|
G | T | 12 | a0001c0001t0001g0224a0001c0001t0003g0069a0001c0001t0004g0093others(9): Show | 12 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+9905G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570341 | ||||||
| chr4:109570379
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9943G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570379 | ||||||
| chr4:109570424
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.99+9988T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570424 | ||||||
| chr4:109570465
|
A | C | 1 | a0003c0003t0001g0316 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+10029A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570465 | ||||||
| chr4:109570493
|
T | C | 1 | a0001c0012t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99+10057T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570493 | ||||||
| chr4:109570509
|
A | C | 25 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+10073A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570509 | ||||||
| chr4:109570556
|
C | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+10120C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570556 | ||||||
| chr4:109570796
|
T | G | 1 | a0001c0001t0001g0323 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.99+10360T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570796 | ||||||
| chr4:109570828
|
C | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+10392C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570828 | ||||||
| chr4:109571092
|
A | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02280.hp1 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+10656A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571092 | ||||||
| chr4:109571120
|
T | G | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+10684T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571120 | ||||||
| chr4:109571303
|
CTTTA | C | 61 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0023others(58): Show | 61 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.99+10891_99+10894d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109571303 | |||||
| chr4:109571314
|
T | G | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+10878T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571314 | ||||||
| chr4:109571452
|
A | G | 2 | a0001c0012t0001g0051a0002c0011t0002g0050 | 2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+11016A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571452 | ||||||
| chr4:109571727
|
T | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(20): Show | 23 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+11291T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571727 | ||||||
| chr4:109571927
|
A | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+11491A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571927 | ||||||
| chr4:109571936
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0052others(24): Show | 27 | HG00738.hp2 HG01975.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.99+11500T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571936 | ||||||
| chr4:109572195
|
G | T | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+11759G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572195 | ||||||
| chr4:109572228
|
C | G | 32 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0224others(29): Show | 32 | HG00438.hp1 HG01884.hp1 HG02004.hp2 others(29): Show |
intron_variant | MODIFIER | c.99+11792C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572228 | ||||||
| chr4:109572307
|
A | G | 98 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+11871A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572307 | ||||||
| chr4:109572312
|
C | A | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+11876C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572312 | ||||||
| chr4:109572380
|
T | G | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+11944T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572380 | ||||||
| chr4:109572428
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+11992A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572428 | ||||||
| chr4:109572642
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99+12206T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572642 | ||||||
| chr4:109572693
|
C | CACTTG | 94 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 94 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.99+12261_99+12262i others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109572693 | |||||
| chr4:109572819
|
C | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12383C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572819 | ||||||
| chr4:109572911
|
G | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(20): Show | 23 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+12475G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572911 | ||||||
| chr4:109573097
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+12661C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573097 | ||||||
| chr4:109573147
|
A | G | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12711A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573147 | ||||||
| chr4:109573250
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12814G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573250 | ||||||
| chr4:109573309
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0004g0016others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+12873C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573309 | ||||||
| chr4:109573361
|
C | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(82): Show | 85 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.99+12925C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573361 | ||||||
| chr4:109573370
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+12934G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573370 | ||||||
| chr4:109573452
|
C | CA | 32 | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0089others(29): Show | 32 | HG00438.hp1 HG00438.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+13031dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573452 | |||||
| chr4:109573490
|
C | T | 1 | a0002c0002t0002g0203 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.99+13054C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573490 | ||||||
| chr4:109573576
|
T | G | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(50): Show | 53 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+13140T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573576 | ||||||
| chr4:109573600
|
G | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(24): Show | 27 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+13164G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573600 | ||||||
| chr4:109573617
|
T | C | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+13181T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573617 | ||||||
| chr4:109573736
|
A | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+13300A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573736 | ||||||
| chr4:109573803
|
G | A | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+13367G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573803 | ||||||
| chr4:109573827
|
G | A | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+13391G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573827 | ||||||
| chr4:109573831
|
G | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 84 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.99+13395G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573831 | ||||||
| chr4:109573867
|
A | AT | 104 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(101): Show | 104 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.99+13454dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | |||||
| chr4:109573867
|
A | ATT | 14 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+13453_99+13454d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | |||||
| chr4:109573867
|
A | ATTT | 14 | a0001c0001t0001g0224a0001c0001t0002g0067a0001c0001t0003g0069others(11): Show | 14 | HG00438.hp1 HG01496.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+13452_99+13454d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | |||||
| chr4:109573867
|
AT | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0213a0001c0001t0002g0044others(17): Show | 20 | HG00544.hp1 HG01168.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+13454delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | |||||
| chr4:109573949
|
T | C | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+13513T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573949 | ||||||
| chr4:109573975
|
C | CAA | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+13539_99+13540i others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573975 | ||||||
| chr4:109573989
|
C | T | 2 | a0001c0012t0001g0051a0002c0011t0002g0050 | 2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+13553C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573989 | ||||||
| chr4:109573997
|
C | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+13561C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573997 | ||||||
| chr4:109574191
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+13755G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574191 | ||||||
| chr4:109574223
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.99+13787T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574223 | ||||||
| chr4:109574269
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 99 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.99+13833A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574269 | ||||||
| chr4:109574442
|
G | A | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+14006G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574442 | ||||||
| chr4:109574502
|
T | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+14066T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574502 | ||||||
| chr4:109574544
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+14108C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574544 | ||||||
| chr4:109574611
|
A | C | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+14175A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574611 | ||||||
| chr4:109574667
|
T | C | 2 | a0001c0012t0001g0051a0002c0011t0002g0050 | 2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+14231T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574667 | ||||||
| chr4:109574702
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(89): Show | 92 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.99+14266A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574702 | ||||||
| chr4:109575048
|
C | T | 2 | a0001c0001t0002g0327a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99+14612C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575048 | ||||||
| chr4:109575169
|
G | T | 5 | a0001c0001t0001g0071a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+14733G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575169 | ||||||
| chr4:109575195
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99+14759C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575195 | ||||||
| chr4:109575350
|
A | G | 19 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0003g0076others(16): Show | 19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+14914A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575350 | ||||||
| chr4:109575438
|
T | C | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+15002T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575438 | ||||||
| chr4:109575514
|
A | G | 16 | a0001c0001t0001g0134a0001c0001t0001g0224a0001c0001t0001g0239others(13): Show | 16 | HG00438.hp1 HG02015.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+15078A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575514 | ||||||
| chr4:109575528
|
C | T | 1 | a0003c0003t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.99+15092C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575528 | ||||||
| chr4:109575610
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0061others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+15174C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575610 | ||||||
| chr4:109575735
|
G | A | 1 | a0003c0003t0001g0084 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.99+15299G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575735 | ||||||
| chr4:109575743
|
A | G | 1 | a0004c0004t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+15307A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575743 | ||||||
| chr4:109575744
|
T | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15308T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575744 | ||||||
| chr4:109575800
|
C | A | 17 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0060others(14): Show | 17 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+15364C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575800 | ||||||
| chr4:109575873
|
G | A | 5 | a0003c0003t0001g0230a0003c0003t0001g0246a0003c0003t0001g0303others(2): Show | 5 | NA18946.hp1 NA18975.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+15437G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575873 | ||||||
| chr4:109575908
|
C | G | 19 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0003g0076others(16): Show | 19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+15472C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575908 | ||||||
| chr4:109576063
|
T | C | 1 | a0003c0003t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.99+15627T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576063 | ||||||
| chr4:109576163
|
C | T | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15727C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576163 | ||||||
| chr4:109576247
|
A | G | 7 | a0001c0001t0001g0071a0001c0001t0003g0011a0002c0002t0002g0010others(4): Show | 7 | HG01175.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15811A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576247 | ||||||
| chr4:109576270
|
C | T | 47 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(44): Show | 47 | HG00438.hp1 HG00639.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.99+15834C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576270 | ||||||
| chr4:109576384
|
A | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15948A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576384 | ||||||
| chr4:109576518
|
C | CT | 179 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0048others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.99+16099dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109576518 | |||||
| chr4:109576518
|
C | CTT | 19 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0062others(16): Show | 19 | HG00621.hp1 HG02280.hp2 HG03130.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+16098_99+16099d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109576518 | |||||
| chr4:109576518
|
CTT | C | 13 | a0001c0001t0001g0089a0001c0001t0003g0077a0001c0001t0003g0079others(10): Show | 13 | HG02071.hp1 HG02165.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+16098_99+16099d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109576518 | |||||
| chr4:109576574
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+16138C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576574 | ||||||
| chr4:109576848
|
C | A | 1 | a0002c0002t0002g0083 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.99+16412C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576848 | ||||||
| chr4:109576913
|
G | A | 1 | a0003c0003t0001g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.99+16477G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576913 | ||||||
| chr4:109576918
|
C | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0017others(161): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.99+16482C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576918 | ||||||
| chr4:109577009
|
G | A | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.99+16573G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577009 | ||||||
| chr4:109577056
|
G | A | 11 | a0001c0001t0005g0095a0001c0001t0005g0097a0001c0001t0005g0099others(8): Show | 11 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+16620G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577056 | ||||||
| chr4:109577368
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(62): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+16932C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577368 | ||||||
| chr4:109577446
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.99+17010G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577446 | ||||||
| chr4:109577447
|
G | A | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+17011G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577447 | ||||||
| chr4:109577584
|
TGGGTACT others(318): Show |
T | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.99+17166_99+17490d others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577584 | |||||
| chr4:109577598
|
C | CT | 36 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0041others(33): Show | 36 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+17191dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | |||||
| chr4:109577598
|
CTTTTTTT others(5): Show |
C | 2 | a0004c0004t0001g0033a0004c0004t0001g0065 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.99+17180_99+17191d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | |||||
| chr4:109577598
|
CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0002g0112 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.99+17176_99+17191d others(18): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | |||||
| chr4:109577598
|
CTTTTTTT others(11): Show |
C | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+17174_99+17191d others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | |||||
| chr4:109577680
|
G | C | 1 | a0002c0002t0002g0137 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.99+17244G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577680 | ||||||
| chr4:109577690
|
G | A | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+17254G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577690 | ||||||
| chr4:109577699
|
C | T | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+17263C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577699 | ||||||
| chr4:109577715
|
A | G | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+17279A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577715 | ||||||
| chr4:109577720
|
C | T | 4 | a0002c0002t0002g0130a0002c0002t0002g0157a0002c0002t0002g0158others(1): Show | 4 | HG00741.hp2 HG01358.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+17284C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577720 | ||||||
| chr4:109577978
|
A | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+17542A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577978 | ||||||
| chr4:109578246
|
A | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+17810A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578246 | ||||||
| chr4:109578254
|
G | A | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+17818G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578254 | ||||||
| chr4:109578493
|
C | CTTT | 12 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(9): Show | 12 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+18068_99+18070d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109578493 | |||||
| chr4:109578521
|
CTG | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+18087_99+18088d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109578521 | |||||
| chr4:109578696
|
C | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0225others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+18260C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578696 | ||||||
| chr4:109578717
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0029 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+18281C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578717 | ||||||
| chr4:109578770
|
A | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+18334A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578770 | ||||||
| chr4:109578802
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+18366A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578802 | ||||||
| chr4:109578847
|
A | T | 3 | a0003c0003t0001g0025a0003c0003t0001g0155a0003c0003t0001g0156 | 3 | HG02717.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.99+18411A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578847 | ||||||
| chr4:109578944
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+18508G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578944 | ||||||
| chr4:109579003
|
C | T | 3 | a0002c0002t0002g0007a0002c0002t0002g0199a0002c0002t0002g0206 | 3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.99+18567C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579003 | ||||||
| chr4:109579255
|
C | CT | 127 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(124): Show | 129 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.99+18832dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109579255 | |||||
| chr4:109579321
|
T | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+18885T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579321 | ||||||
| chr4:109579367
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+18931A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579367 | ||||||
| chr4:109579394
|
C | T | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+18958C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579394 | ||||||
| chr4:109579406
|
C | T | 35 | a0001c0001t0001g0089a0001c0001t0001g0300a0001c0001t0001g0301others(32): Show | 36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+18970C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579406 | ||||||
| chr4:109579407
|
GC | G | 10 | a0001c0001t0001g0049a0001c0001t0001g0280a0001c0001t0002g0327others(7): Show | 10 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+18974delC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109579407 | |||||
| chr4:109579439
|
G | A | 1 | a0001c0012t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99+19003G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579439 | ||||||
| chr4:109579507
|
C | T | 1 | a0001c0001t0005g0095 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+19071C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579507 | ||||||
| chr4:109579598
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+19162G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579598 | ||||||
| chr4:109579655
|
A | C | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.99+19219A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579655 | ||||||
| chr4:109579666
|
G | A | 1 | a0003c0003t0001g0321 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.99+19230G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579666 | ||||||
| chr4:109579928
|
C | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.99+19492C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579928 | ||||||
| chr4:109579931
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(62): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+19495C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579931 | ||||||
| chr4:109579941
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG00735.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+19505G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579941 | ||||||
| chr4:109580124
|
G | A | 1 | a0003c0003t0001g0310 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.99+19688G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580124 | ||||||
| chr4:109580356
|
G | A | 1 | a0003c0003t0001g0255 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+19920G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580356 | ||||||
| chr4:109580397
|
T | C | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+19961T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580397 | ||||||
| chr4:109580438
|
C | T | 6 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0059others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+20002C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580438 | ||||||
| chr4:109580508
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0003g0131a0001c0001t0003g0135others(2): Show | 5 | NA18939.hp2 NA18947.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+20072C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580508 | ||||||
| chr4:109580509
|
G | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+20073G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580509 | ||||||
| chr4:109580590
|
C | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+20154C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580590 | ||||||
| chr4:109580764
|
T | C | 3 | a0001c0001t0002g0327a0001c0005t0006g0169a0001c0005t0006g0326 | 3 | HG00738.hp2 HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.99+20328T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580764 | ||||||
| chr4:109580795
|
C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.99+20359C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580795 | ||||||
| chr4:109580823
|
G | A | 4 | a0001c0001t0001g0256a0003c0003t0001g0282a0003c0003t0001g0318others(1): Show | 4 | NA18939.hp1 NA18986.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+20387G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580823 | ||||||
| chr4:109580860
|
T | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0105 | 3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+20424T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580860 | ||||||
| chr4:109580897
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0004g0126 | 3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+20461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580897 | ||||||
| chr4:109581031
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+20595T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581031 | ||||||
| chr4:109581262
|
A | T | 1 | a0003c0003t0001g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+20826A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581262 | ||||||
| chr4:109581339
|
C | T | 1 | a0002c0002t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+20903C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581339 | ||||||
| chr4:109581370
|
G | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 10 | HG00639.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+20934G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581370 | ||||||
| chr4:109581498
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.99+21062C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581498 | ||||||
| chr4:109581522
|
AT | A | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+21088delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109581522 | |||||
| chr4:109581633
|
T | C | 1 | a0002c0002t0002g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.99+21197T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581633 | ||||||
| chr4:109581773
|
A | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+21337A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581773 | ||||||
| chr4:109581824
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+21388G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581824 | ||||||
| chr4:109581954
|
C | T | 1 | a0002c0002t0002g0007 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.99+21518C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581954 | ||||||
| chr4:109581972
|
G | A | 1 | a0002c0002t0002g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99+21536G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581972 | ||||||
| chr4:109581974
|
T | A | 1 | a0002c0002t0002g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99+21538T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581974 | ||||||
| chr4:109582024
|
G | A | 1 | a0004c0004t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.99+21588G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582024 | ||||||
| chr4:109582025
|
C | G | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+21589C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582025 | ||||||
| chr4:109582149
|
C | T | 59 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0111others(56): Show | 59 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.99+21713C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582149 | ||||||
| chr4:109582150
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+21714G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582150 | ||||||
| chr4:109582167
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+21731C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582167 | ||||||
| chr4:109582198
|
T | TA | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+21768dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582198 | |||||
| chr4:109582231
|
C | G | 3 | a0001c0001t0001g0325a0001c0005t0006g0046a0005c0009t0001g0226 | 3 | HG02257.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+21795C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582231 | ||||||
| chr4:109582270
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+21834T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582270 | ||||||
| chr4:109582295
|
C | T | 1 | a0001c0001t0005g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+21859C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582295 | ||||||
| chr4:109582389
|
A | AG | 8 | a0001c0001t0001g0183a0001c0001t0003g0198a0001c0001t0004g0059others(5): Show | 8 | HG01433.hp2 HG02738.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+21959dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582389 | |||||
| chr4:109582389
|
A | G | 1 | a0001c0001t0002g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+21953A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582389 | ||||||
| chr4:109582494
|
G | C | 3 | a0001c0001t0002g0327a0001c0005t0006g0169a0001c0005t0006g0326 | 3 | HG00738.hp2 HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.99+22058G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582494 | ||||||
| chr4:109582538
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+22102T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582538 | ||||||
| chr4:109582538
|
T | TA | 20 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+22112dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582538 | |||||
| chr4:109582539
|
A | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+22103A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582539 | ||||||
| chr4:109582560
|
C | CAA | 10 | a0001c0001t0005g0095a0001c0001t0005g0099a0001c0001t0005g0115others(7): Show | 10 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+22139_99+22140d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582560 | |||||
| chr4:109582560
|
CA | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(298): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.99+22140delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582560 | |||||
| chr4:109582564
|
A | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(68): Show | 74 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.99+22128A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582564 | ||||||
| chr4:109582567
|
A | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+22131A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582567 | ||||||
| chr4:109582570
|
A | C | 4 | a0001c0001t0001g0048a0001c0001t0009g0108a0001c0005t0006g0169others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+22134A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582570 | ||||||
| chr4:109582606
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+22170C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582606 | ||||||
| chr4:109582618
|
G | C | 10 | a0002c0002t0002g0129a0002c0002t0002g0139a0002c0002t0002g0159others(7): Show | 10 | HG01168.hp1 HG01346.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+22182G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582618 | ||||||
| chr4:109582727
|
T | C | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+22291T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582727 | ||||||
| chr4:109583091
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+22655T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583091 | ||||||
| chr4:109583094
|
G | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0004g0126 | 3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+22658G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583094 | ||||||
| chr4:109583110
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+22674A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583110 | ||||||
| chr4:109583114
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0047 | 3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+22678C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583114 | ||||||
| chr4:109583153
|
C | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0173a0001c0001t0001g0181others(11): Show | 14 | HG02071.hp1 NA18747.hp1 NA18957.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+22717C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583153 | ||||||
| chr4:109583160
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.99+22724G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583160 | ||||||
| chr4:109583187
|
A | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+22751A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583187 | ||||||
| chr4:109583194
|
G | T | 1 | a0002c0002t0002g0278 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+22758G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583194 | ||||||
| chr4:109583282
|
C | T | 1 | a0003c0003t0001g0164 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+22846C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583282 | ||||||
| chr4:109583375
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+22939T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583375 | ||||||
| chr4:109583418
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+22982C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583418 | ||||||
| chr4:109583597
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+23161G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583597 | ||||||
| chr4:109583599
|
G | A | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+23163G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583599 | ||||||
| chr4:109583729
|
T | C | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+23293T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583729 | ||||||
| chr4:109583791
|
G | A | 4 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136others(1): Show | 5 | NA18964.hp1 NA18970.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+23355G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583791 | ||||||
| chr4:109583815
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.99+23379G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583815 | ||||||
| chr4:109583911
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+23475G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583911 | ||||||
| chr4:109584025
|
T | C | 1 | a0004c0004t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.99+23589T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584025 | ||||||
| chr4:109584102
|
TATTA | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+23671_99+23674d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109584102 | |||||
| chr4:109584190
|
G | T | 1 | a0002c0002t0002g0161 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.99+23754G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584190 | ||||||
| chr4:109584364
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+23928C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584364 | ||||||
| chr4:109584388
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.99+23952T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584388 | ||||||
| chr4:109584699
|
C | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24263C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584699 | ||||||
| chr4:109584753
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+24317T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584753 | ||||||
| chr4:109584888
|
G | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24452G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584888 | ||||||
| chr4:109584900
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.99+24464T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584900 | ||||||
| chr4:109584936
|
G | C | 2 | a0004c0004t0001g0251a0004c0004t0001g0284 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.99+24500G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584936 | ||||||
| chr4:109584938
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+24502G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584938 | ||||||
| chr4:109584988
|
T | G | 2 | a0001c0001t0003g0011a0002c0002t0002g0010 | 2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99+24552T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584988 | ||||||
| chr4:109585013
|
A | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24577A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585013 | ||||||
| chr4:109585023
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24587G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585023 | ||||||
| chr4:109585125
|
G | GT | 5 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0165others(2): Show | 5 | HG00323.hp1 HG00642.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+24690dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109585125 | |||||
| chr4:109585354
|
G | C | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+24918G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585354 | ||||||
| chr4:109585384
|
G | T | 1 | a0002c0002t0002g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+24948G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585384 | ||||||
| chr4:109585489
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.99+25053T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585489 | ||||||
| chr4:109585652
|
A | G | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+25216A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585652 | ||||||
| chr4:109585768
|
A | G | 2 | a0001c0001t0001g0068a0004c0004t0001g0035 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99+25332A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585768 | ||||||
| chr4:109585817
|
G | T | 1 | a0002c0002t0002g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.99+25381G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585817 | ||||||
| chr4:109585885
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+25449T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585885 | ||||||
| chr4:109585978
|
T | C | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+25542T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585978 | ||||||
| chr4:109586043
|
C | T | 1 | a0002c0002t0002g0083 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.99+25607C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586043 | ||||||
| chr4:109586044
|
G | A | 3 | a0002c0002t0002g0007a0002c0002t0002g0199a0002c0002t0002g0206 | 3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.99+25608G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586044 | ||||||
| chr4:109586173
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0280others(9): Show | 12 | HG00735.hp2 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+25737C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586173 | ||||||
| chr4:109586205
|
C | T | 1 | a0003c0003t0001g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.99+25769C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586205 | ||||||
| chr4:109586279
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+25843C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586279 | ||||||
| chr4:109586298
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+25862C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586298 | ||||||
| chr4:109586342
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+25906G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586342 | ||||||
| chr4:109586447
|
A | G | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+26011A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586447 | ||||||
| chr4:109586507
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+26071T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586507 | ||||||
| chr4:109586598
|
G | A | 1 | a0001c0001t0003g0079 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.99+26162G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586598 | ||||||
| chr4:109586612
|
G | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+26176G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586612 | ||||||
| chr4:109586632
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+26196G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586632 | ||||||
| chr4:109586735
|
T | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+26299T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586735 | ||||||
| chr4:109586832
|
T | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+26396T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586832 | ||||||
| chr4:109586913
|
C | T | 35 | a0001c0001t0001g0089a0001c0001t0001g0300a0001c0001t0001g0301others(32): Show | 36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+26477C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586913 | ||||||
| chr4:109587074
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+26638C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587074 | ||||||
| chr4:109587088
|
C | T | 1 | a0002c0002t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.99+26652C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587088 | ||||||
| chr4:109587123
|
A | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+26687A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587123 | ||||||
| chr4:109587166
|
C | T | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+26730C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587166 | ||||||
| chr4:109587247
|
G | C | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+26811G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587247 | ||||||
| chr4:109587332
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+26896G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587332 | ||||||
| chr4:109587363
|
T | C | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+26927T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587363 | ||||||
| chr4:109587425
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+26989G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587425 | ||||||
| chr4:109587426
|
A | ATGCCC | 40 | a0001c0001t0001g0089a0001c0001t0001g0300a0001c0001t0001g0301others(37): Show | 41 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.99+26998_99+27002d others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109587426 | |||||
| chr4:109587449
|
G | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+27013G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587449 | ||||||
| chr4:109587500
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99+27064G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587500 | ||||||
| chr4:109587529
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+27093C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587529 | ||||||
| chr4:109587530
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0004g0126 | 3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+27094G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587530 | ||||||
| chr4:109587532
|
C | T | 9 | a0001c0001t0001g0068a0002c0002t0002g0012a0004c0004t0001g0013others(6): Show | 9 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+27096C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587532 | ||||||
| chr4:109587547
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 10 | HG00639.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+27111C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587547 | ||||||
| chr4:109587563
|
C | T | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+27127C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587563 | ||||||
| chr4:109587571
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.99+27135G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587571 | ||||||
| chr4:109587580
|
C | A | 1 | a0003c0003t0001g0255 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+27144C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587580 | ||||||
| chr4:109587589
|
T | G | 1 | a0001c0005t0006g0326 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.99+27153T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587589 | ||||||
| chr4:109587595
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+27159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587595 | ||||||
| chr4:109587682
|
G | T | 3 | a0002c0011t0002g0050a0004c0004t0001g0037a0004c0004t0001g0078 | 3 | HG02145.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+27246G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587682 | ||||||
| chr4:109587713
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+27277G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587713 | ||||||
| chr4:109587717
|
C | CTA | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+27281_99+27282i others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587717 | ||||||
| chr4:109587817
|
T | C | 1 | a0001c0001t0003g0069 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+27381T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587817 | ||||||
| chr4:109588030
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+27594G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588030 | ||||||
| chr4:109588207
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+27771A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588207 | ||||||
| chr4:109588270
|
C | T | 2 | a0001c0001t0001g0048a0004c0004t0001g0047 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.99+27834C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588270 | ||||||
| chr4:109588322
|
G | C | 1 | a0001c0001t0003g0069 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+27886G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588322 | ||||||
| chr4:109588333
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0293a0001c0001t0001g0298others(1): Show | 4 | HG00735.hp1 HG02109.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+27897A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588333 | ||||||
| chr4:109588334
|
A | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+27898A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588334 | ||||||
| chr4:109588407
|
C | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+27971C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588407 | ||||||
| chr4:109588470
|
G | T | 1 | a0004c0004t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+28034G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588470 | ||||||
| chr4:109588617
|
C | A | 1 | a0001c0001t0004g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+28181C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588617 | ||||||
| chr4:109588872
|
A | T | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+28436A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588872 | ||||||
| chr4:109588924
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+28488G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588924 | ||||||
| chr4:109588978
|
G | GA | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+28551dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109588978 | |||||
| chr4:109589063
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+28627T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589063 | ||||||
| chr4:109589186
|
C | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+28750C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589186 | ||||||
| chr4:109589417
|
C | T | 1 | a0002c0002t0002g0278 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+28981C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589417 | ||||||
| chr4:109589535
|
C | T | 1 | a0003c0003t0001g0277 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+29099C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589535 | ||||||
| chr4:109589553
|
C | G | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+29117C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589553 | ||||||
| chr4:109589602
|
AT | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+29168delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109589602 | |||||
| chr4:109589699
|
C | G | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+29263C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589699 | ||||||
| chr4:109589790
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0004g0126 | 3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+29354C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589790 | ||||||
| chr4:109589811
|
G | A | 1 | a0001c0001t0003g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+29375G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589811 | ||||||
| chr4:109589813
|
G | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+29377G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589813 | ||||||
| chr4:109589836
|
T | G | 4 | a0001c0001t0005g0279a0003c0003t0001g0257a0003c0003t0001g0258others(1): Show | 4 | HG02083.hp2 HG02129.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+29400T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589836 | ||||||
| chr4:109590075
|
A | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+29639A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590075 | ||||||
| chr4:109590185
|
GAGTA | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+29755_99+29758d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109590185 | |||||
| chr4:109590472
|
T | C | 1 | a0003c0003t0001g0216 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.99+30036T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590472 | ||||||
| chr4:109590534
|
G | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+30098G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590534 | ||||||
| chr4:109590805
|
T | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+30369T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590805 | ||||||
| chr4:109590923
|
A | G | 1 | a0002c0002t0002g0206 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.99+30487A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590923 | ||||||
| chr4:109591185
|
C | CT | 36 | a0001c0001t0001g0032a0001c0001t0001g0060a0001c0001t0001g0061others(33): Show | 36 | HG00438.hp1 HG00621.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+30764dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109591185 | |||||
| chr4:109591185
|
CT | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0280others(11): Show | 14 | HG00735.hp2 HG00738.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+30764delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109591185 | |||||
| chr4:109591337
|
T | C | 143 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(140): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.99+30901T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591337 | ||||||
| chr4:109591421
|
G | A | 1 | a0003c0003t0001g0260 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.99+30985G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591421 | ||||||
| chr4:109591501
|
T | C | 9 | a0001c0001t0001g0068a0002c0002t0002g0012a0004c0004t0001g0013others(6): Show | 9 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+31065T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591501 | ||||||
| chr4:109591569
|
G | A | 1 | a0002c0002t0002g0283 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.99+31133G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591569 | ||||||
| chr4:109591644
|
A | G | 1 | a0002c0002t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+31208A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591644 | ||||||
| chr4:109591668
|
T | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0280others(6): Show | 9 | HG00735.hp2 HG00738.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+31232T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591668 | ||||||
| chr4:109591730
|
G | A | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+31294G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591730 | ||||||
| chr4:109591765
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.99+31329T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591765 | ||||||
| chr4:109591774
|
C | G | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+31338C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591774 | ||||||
| chr4:109591803
|
A | G | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+31367A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591803 | ||||||
| chr4:109591957
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+31521C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591957 | ||||||
| chr4:109591967
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+31531T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591967 | ||||||
| chr4:109591988
|
C | T | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+31552C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591988 | ||||||
| chr4:109592054
|
C | A | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+31618C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592054 | ||||||
| chr4:109592144
|
C | T | 123 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.99+31708C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592144 | ||||||
| chr4:109592335
|
G | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0309 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.99+31899G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592335 | ||||||
| chr4:109592345
|
G | A | 3 | a0001c0001t0001g0325a0001c0005t0006g0046a0005c0009t0001g0226 | 3 | HG02257.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+31909G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592345 | ||||||
| chr4:109592481
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.99+32045C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592481 | ||||||
| chr4:109592686
|
A | G | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+32250A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592686 | ||||||
| chr4:109592689
|
T | C | 1 | a0002c0002t0010g0237 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.99+32253T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592689 | ||||||
| chr4:109592749
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+32313A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592749 | ||||||
| chr4:109592826
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+32390A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592826 | ||||||
| chr4:109592827
|
C | G | 3 | a0001c0001t0001g0032a0001c0001t0002g0038a0001c0001t0002g0067 | 3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+32391C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592827 | ||||||
| chr4:109592974
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+32538C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592974 | ||||||
| chr4:109593034
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+32598C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593034 | ||||||
| chr4:109593068
|
A | G | 21 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+32632A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593068 | ||||||
| chr4:109593122
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(1): Show | 4 | HG00639.hp1 HG02486.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+32686C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593122 | ||||||
| chr4:109593123
|
G | A | 1 | a0004c0004t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+32687G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593123 | ||||||
| chr4:109593135
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.99+32699C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593135 | ||||||
| chr4:109593159
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+32723A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593159 | ||||||
| chr4:109593181
|
G | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+32745G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593181 | ||||||
| chr4:109593303
|
CAG | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(63): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+32868_99+32869d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593303 | ||||||
| chr4:109593375
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+32939C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593375 | ||||||
| chr4:109593514
|
G | A | 2 | a0001c0001t0003g0036a0001c0001t0003g0087 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+33078G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593514 | ||||||
| chr4:109593545
|
A | G | 1 | a0002c0002t0002g0152 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.99+33109A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593545 | ||||||
| chr4:109593660
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+33224G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593660 | ||||||
| chr4:109593761
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99+33325G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593761 | ||||||
| chr4:109593791
|
A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.99+33355A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593791 | ||||||
| chr4:109593970
|
G | A | 2 | a0001c0001t0003g0076a0002c0002t0002g0083 | 2 | HG02080.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.99+33534G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593970 | ||||||
| chr4:109594135
|
G | A | 1 | a0002c0002t0002g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+33699G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594135 | ||||||
| chr4:109594203
|
G | A | 21 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+33767G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594203 | ||||||
| chr4:109594315
|
G | A | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+33879G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594315 | ||||||
| chr4:109594328
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(171): Show | 179 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.99+33892A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594328 | ||||||
| chr4:109594358
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+33922C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594358 | ||||||
| chr4:109594405
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(97): Show | 103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.99+33969A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594405 | ||||||
| chr4:109594491
|
A | G | 1 | a0003c0003t0001g0289 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.99+34055A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594491 | ||||||
| chr4:109594583
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+34147C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594583 | ||||||
| chr4:109594771
|
TTC | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+34339_99+34340d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109594771 | |||||
| chr4:109594778
|
T | C | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+34342T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594778 | ||||||
| chr4:109594779
|
C | T | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+34343C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594779 | ||||||
| chr4:109594779
|
CT | C | 8 | a0001c0001t0001g0187a0001c0001t0005g0196a0001c0006t0005g0002others(5): Show | 9 | HG01975.hp1 HG02155.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+34356delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109594779 | |||||
| chr4:109594785
|
T | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+34349T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594785 | ||||||
| chr4:109594854
|
A | AAAT | 21 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0071others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+34420_99+34422d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109594854 | |||||
| chr4:109594876
|
C | T | 1 | a0002c0002t0002g0103 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.99+34440C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594876 | ||||||
| chr4:109594959
|
C | T | 3 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0002t0002g0074 | 3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.99+34523C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594959 | ||||||
| chr4:109594995
|
C | G | 1 | a0002c0002t0002g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+34559C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594995 | ||||||
| chr4:109595140
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+34704T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595140 | ||||||
| chr4:109595179
|
G | C | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+34743G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595179 | ||||||
| chr4:109595205
|
T | C | 33 | a0001c0001t0001g0089a0001c0001t0003g0003a0001c0001t0003g0011others(30): Show | 34 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+34769T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595205 | ||||||
| chr4:109595304
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+34868T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595304 | ||||||
| chr4:109595386
|
G | A | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+34950G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595386 | ||||||
| chr4:109595511
|
A | AT | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+35076dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109595511 | |||||
| chr4:109595619
|
C | A | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+35183C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595619 | ||||||
| chr4:109595627
|
A | G | 5 | a0003c0003t0001g0230a0003c0003t0001g0246a0003c0003t0001g0303others(2): Show | 5 | NA18946.hp1 NA18975.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+35191A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595627 | ||||||
| chr4:109595743
|
G | A | 1 | a0002c0002t0002g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.99+35307G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595743 | ||||||
| chr4:109595918
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+35482G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595918 | ||||||
| chr4:109595952
|
C | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+35516C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595952 | ||||||
| chr4:109596023
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+35587C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596023 | ||||||
| chr4:109596027
|
C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+35591C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596027 | ||||||
| chr4:109596236
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+35800G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596236 | ||||||
| chr4:109596287
|
A | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+35851A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596287 | ||||||
| chr4:109596299
|
A | G | 1 | a0001c0001t0004g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99+35863A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596299 | ||||||
| chr4:109596307
|
G | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+35871G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596307 | ||||||
| chr4:109596388
|
AGAG | A | 8 | a0001c0001t0001g0068a0004c0004t0001g0013a0004c0004t0001g0028others(5): Show | 8 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+35957_99+35959d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596388 | |||||
| chr4:109596541
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+36105T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596541 | ||||||
| chr4:109596668
|
G | T | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+36232G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596668 | ||||||
| chr4:109596721
|
ACTT | A | 6 | a0002c0002t0002g0278a0003c0003t0001g0216a0003c0003t0001g0261others(3): Show | 6 | HG01257.hp2 HG01891.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+36289_99+36291d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596721 | |||||
| chr4:109596723
|
TTC | T | 67 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(64): Show | 69 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.99+36289_99+36290d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596723 | |||||
| chr4:109596725
|
C | CT | 82 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(79): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.99+36303dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596725 | |||||
| chr4:109596739
|
T | TA | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+36305dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596739 | |||||
| chr4:109596801
|
A | G | 1 | a0002c0002t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99+36365A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596801 | ||||||
| chr4:109596877
|
C | T | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+36441C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596877 | ||||||
| chr4:109596929
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+36493C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596929 | ||||||
| chr4:109596940
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+36504A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596940 | ||||||
| chr4:109597098
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+36662A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597098 | ||||||
| chr4:109597178
|
C | T | 1 | a0003c0003t0001g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+36742C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597178 | ||||||
| chr4:109597211
|
G | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+36775G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597211 | ||||||
| chr4:109597230
|
T | C | 1 | a0003c0003t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36794T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597230 | ||||||
| chr4:109597232
|
T | C | 1 | a0003c0003t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36796T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597232 | ||||||
| chr4:109597241
|
T | C | 1 | a0003c0003t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36805T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597241 | ||||||
| chr4:109597243
|
T | C | 1 | a0003c0003t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36807T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597243 | ||||||
| chr4:109597310
|
C | T | 7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+36874C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597310 | ||||||
| chr4:109597320
|
T | C | 1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+36884T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597320 | ||||||
| chr4:109597335
|
A | AGACGGGG others(42): Show |
2 | a0001c0001t0001g0048a0004c0004t0001g0047 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.99+36929_99+36930i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(42): Show |
6 | a0001c0001t0001g0225a0001c0001t0001g0280a0001c0001t0001g0300others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+37067_99+37115d others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(91): Show |
34 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0325others(31): Show | 35 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+37018_99+37115d others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(140): Show |
1 | a0005c0009t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+36969_99+37115d others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(42): Show |
2 | a0003c0003t0001g0281a0003c0003t0001g0285 | 2 | HG04115.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.99+36930_99+36931i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(140): Show |
6 | a0003c0003t0001g0004a0003c0003t0001g0272a0003c0003t0001g0273others(3): Show | 7 | HG01978.hp2 HG03491.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+36930_99+36931i others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(189): Show |
51 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0005g0279others(48): Show | 52 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(238): Show |
3 | a0002c0002t0002g0090a0003c0003t0001g0286a0003c0003t0001g0287 | 3 | HG02004.hp2 HG04204.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.99+36930_99+36931i others(247): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(239): Show |
1 | a0002c0002t0002g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(248): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(189): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0040others(3): Show | 7 | HG01891.hp2 HG01975.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(190): Show |
1 | a0001c0001t0001g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(140): Show |
1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(190): Show |
1 | a0003c0003t0001g0275 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.99+36930_99+36931i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(91): Show |
1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+36930_99+36931i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(190): Show |
1 | a0007c0010t0001g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(189): Show |
1 | a0002c0002t0002g0311 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | AGACGGGG others(42): Show |
1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+36929_99+36930i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
A | G | 1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+36899A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597335 | ||||||
| chr4:109597335
|
AGACGGGG others(42): Show |
A | 21 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+37067_99+37115d others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597335
|
AGACGGGG others(140): Show |
A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+36969_99+37115d others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | |||||
| chr4:109597338
|
C | G | 1 | a0001c0001t0005g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+36902C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597338 | ||||||
| chr4:109597356
|
G | A | 3 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0002t0002g0074 | 3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.99+36920G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597356 | ||||||
| chr4:109597356
|
G | GGGGGGCT others(189): Show |
1 | a0003c0003t0001g0313 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597356 | |||||
| chr4:109597365
|
A | ACCCCCCC others(92): Show |
3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+36936_99+37034d others(101): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597365 | |||||
| chr4:109597365
|
A | ACTCCCCC others(191): Show |
1 | a0003c0003t0001g0305 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(200): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597365 | |||||
| chr4:109597367
|
C | T | 87 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.99+36931C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597367 | ||||||
| chr4:109597387
|
C | G | 19 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+36951C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597387 | ||||||
| chr4:109597416
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.99+36980C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597416 | ||||||
| chr4:109597424
|
C | CTCCCTCC others(91): Show |
4 | a0001c0001t0001g0089a0001c0001t0003g0135a0001c0001t0003g0329others(1): Show | 4 | NA18939.hp2 NA18947.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+37085_99+37086i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597424 | |||||
| chr4:109597433
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.99+36997G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597433 | ||||||
| chr4:109597437
|
G | GGGGCGGC others(91): Show |
1 | a0001c0005t0006g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+37098_99+37099i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597437 | |||||
| chr4:109597441
|
C | CGGCTGGC others(288): Show |
1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+37083_99+37084i others(297): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597441 | |||||
| chr4:109597441
|
C | T | 46 | a0001c0001t0003g0069a0001c0001t0005g0279a0002c0002t0002g0278others(43): Show | 48 | HG00280.hp1 HG01071.hp1 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.99+37005C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597441 | ||||||
| chr4:109597442
|
GGCTGGCC others(169): Show |
G | 1 | a0001c0001t0001g0299 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99+37029_99+37204d others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597442 | |||||
| chr4:109597453
|
C | CGGGGGGC others(91): Show |
2 | a0002c0002t0002g0141a0002c0002t0002g0203 | 2 | NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.99+37094_99+37095i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | CGGGGGGC others(90): Show |
1 | a0002c0002t0002g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+37018_99+37114d others(99): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | CGGGGGGC others(91): Show |
60 | a0001c0001t0001g0140a0001c0005t0002g0253a0002c0002t0002g0007others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.99+37114_99+37115i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | CGGGGGGC others(92): Show |
7 | a0002c0002t0002g0110a0002c0002t0002g0116a0002c0002t0002g0138others(4): Show | 7 | HG00438.hp2 HG00544.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+37114_99+37115i others(101): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | CGGGGGGC others(93): Show |
1 | a0004c0004t0001g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+37083_99+37084i others(102): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | CGGGGGGC others(92): Show |
1 | a0002c0002t0002g0160 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.99+37072_99+37073i others(101): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | CGGGGGGC others(42): Show |
3 | a0002c0002t0002g0117a0002c0002t0002g0127a0002c0002t0002g0205 | 3 | HG01175.hp2 NA18949.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.99+37065_99+37066i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | |||||
| chr4:109597453
|
C | T | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+37017C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597453 | ||||||
| chr4:109597463
|
A | ACCCCCCC others(190): Show |
1 | a0003c0003t0001g0235 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597463 | |||||
| chr4:109597463
|
A | ACCCCCCC others(94): Show |
1 | a0002c0002t0002g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99+37034_99+37035i others(103): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597463 | |||||
| chr4:109597464
|
CCCCCCCA others(41): Show |
C | 1 | a0001c0001t0005g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+37035_99+37082d others(50): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597464 | |||||
| chr4:109597498
|
C | A | 2 | a0001c0001t0001g0213a0002c0002t0002g0182 | 2 | NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.99+37062C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597498 | ||||||
| chr4:109597499
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+37063G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597499 | ||||||
| chr4:109597502
|
C | CGGGGGGC others(189): Show |
1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.99+37091_99+37092i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597502 | |||||
| chr4:109597502
|
C | CGGGGGGC others(190): Show |
1 | a0001c0001t0001g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+37091_99+37092i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597502 | |||||
| chr4:109597502
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0032others(6): Show | 10 | HG01891.hp2 HG01975.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+37066C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597502 | ||||||
| chr4:109597503
|
G | GGGGGGCT others(91): Show |
1 | a0002c0002t0002g0142 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99+37114_99+37115i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597503 | |||||
| chr4:109597512
|
A | ACCCCCCC others(142): Show |
1 | a0003c0003t0001g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(151): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597512 | |||||
| chr4:109597513
|
C | CCCCCCCA others(90): Show |
9 | a0001c0001t0001g0068a0004c0004t0001g0013a0004c0004t0001g0028others(6): Show | 9 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+37115_99+37116i others(99): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597513 | |||||
| chr4:109597531
|
G | GGACGGGG others(189): Show |
1 | a0003c0003t0001g0260 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.99+37115_99+37116i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597531 | |||||
| chr4:109597531
|
G | GGACGGGG others(189): Show |
2 | a0001c0001t0004g0058a0003c0003t0001g0265 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.99+37115_99+37116i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597531 | |||||
| chr4:109597535
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0026others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.99+37099G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597535 | ||||||
| chr4:109597535
|
G | GGGGCGGC others(189): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+37115_99+37116i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597535 | |||||
| chr4:109597535
|
G | GGGGCGGC others(140): Show |
1 | a0001c0001t0001g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597535 | |||||
| chr4:109597535
|
G | GGGGCGGC others(141): Show |
1 | a0001c0001t0001g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(150): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597535 | |||||
| chr4:109597540
|
G | A | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+37104G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597540 | ||||||
| chr4:109597580
|
C | T | 75 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(72): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.99+37144C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597580 | ||||||
| chr4:109597595
|
G | A | 1 | a0005c0009t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+37159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597595 | ||||||
| chr4:109597625
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+37189C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597625 | ||||||
| chr4:109597626
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0047 | 3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+37190G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597626 | ||||||
| chr4:109597660
|
ACCGGGCG others(5): Show |
A | 1 | a0004c0004t0001g0331 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+37233_99+37244d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597660 | |||||
| chr4:109597662
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37226C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597662 | ||||||
| chr4:109597662
|
CGGGCGGC others(41): Show |
C | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+37259_99+37306d others(50): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597662 | |||||
| chr4:109597705
|
TGGACGGG others(42): Show |
T | 13 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(10): Show | 14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+37278_99+37326d others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597705 | |||||
| chr4:109597709
|
C | T | 13 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(10): Show | 13 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+37273C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597709 | ||||||
| chr4:109597726
|
C | T | 77 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(74): Show | 79 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.99+37290C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597726 | ||||||
| chr4:109597732
|
G | C | 4 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0236others(1): Show | 5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+37296G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597732 | ||||||
| chr4:109597732
|
G | T | 1 | a0003c0003t0001g0281 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.99+37296G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597732 | ||||||
| chr4:109597736
|
A | AC | 19 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+37307dupC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597736 | |||||
| chr4:109597754
|
C | T | 153 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0061others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.99+37318C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597754 | ||||||
| chr4:109597759
|
G | A | 1 | a0002c0002t0002g0206 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.99+37323G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597759 | ||||||
| chr4:109597777
|
A | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+37341A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597777 | ||||||
| chr4:109597804
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+37368A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597804 | ||||||
| chr4:109597815
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+37379A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597815 | ||||||
| chr4:109597897
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+37461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597897 | ||||||
| chr4:109597946
|
C | T | 1 | a0002c0002t0002g0199 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.99+37510C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597946 | ||||||
| chr4:109597951
|
C | T | 2 | a0003c0003t0001g0246a0003c0003t0001g0305 | 2 | NA18946.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.99+37515C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597951 | ||||||
| chr4:109597955
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+37519T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597955 | ||||||
| chr4:109597956
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+37520G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597956 | ||||||
| chr4:109597969
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+37533A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597969 | ||||||
| chr4:109598013
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+37577C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598013 | ||||||
| chr4:109598043
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+37607C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598043 | ||||||
| chr4:109598093
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+37657C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598093 | ||||||
| chr4:109598144
|
C | T | 2 | a0001c0001t0003g0036a0001c0001t0003g0087 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+37708C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598144 | ||||||
| chr4:109598155
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.99+37719C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598155 | ||||||
| chr4:109598156
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+37720A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598156 | ||||||
| chr4:109598171
|
C | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37735C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598171 | ||||||
| chr4:109598187
|
C | CG | 9 | a0001c0001t0001g0239a0001c0001t0004g0016a0001c0001t0004g0055others(6): Show | 9 | HG00621.hp2 HG01928.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+37755dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109598187 | |||||
| chr4:109598188
|
G | A | 1 | a0002c0002t0002g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+37752G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598188 | ||||||
| chr4:109598199
|
C | T | 83 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(80): Show | 85 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.99+37763C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598199 | ||||||
| chr4:109598244
|
G | A | 2 | a0004c0004t0001g0037a0004c0004t0001g0078 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.99+37808G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598244 | ||||||
| chr4:109598267
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37831G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598267 | ||||||
| chr4:109598279
|
T | C | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.99+37843T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598279 | ||||||
| chr4:109598297
|
G | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+37861G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598297 | ||||||
| chr4:109598323
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37887G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598323 | ||||||
| chr4:109598329
|
C | T | 1 | a0003c0003t0001g0320 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99+37893C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598329 | ||||||
| chr4:109598368
|
G | A | 49 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+37932G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598368 | ||||||
| chr4:109598395
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+37959C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598395 | ||||||
| chr4:109598422
|
G | A | 2 | a0001c0001t0001g0213a0002c0002t0002g0182 | 2 | NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.99+37986G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598422 | ||||||
| chr4:109598426
|
C | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37990C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598426 | ||||||
| chr4:109598427
|
C | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37991C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598427 | ||||||
| chr4:109598452
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+38016C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598452 | ||||||
| chr4:109598502
|
A | C | 2 | a0002c0002t0002g0109a0002c0002t0002g0110 | 2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.99+38066A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598502 | ||||||
| chr4:109598502
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+38066A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598502 | ||||||
| chr4:109598538
|
T | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01243.hp1 HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.99+38102T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598538 | ||||||
| chr4:109598553
|
C | A | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+38117C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598553 | ||||||
| chr4:109598574
|
A | G | 3 | a0002c0002t0002g0130a0002c0002t0002g0157a0002c0002t0002g0215 | 3 | HG00741.hp2 HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.99+38138A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598574 | ||||||
| chr4:109598582
|
CGTGGAAA others(18): Show |
C | 27 | a0001c0001t0001g0089a0001c0001t0003g0076a0001c0001t0003g0077others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+38151_99+38175d others(27): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109598582 | |||||
| chr4:109598583
|
G | A | 69 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.99+38147G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598583 | ||||||
| chr4:109598607
|
G | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(222): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.99+38171G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598607 | ||||||
| chr4:109598608
|
G | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+38172G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598608 | ||||||
| chr4:109598615
|
G | A | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+38179G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598615 | ||||||
| chr4:109598617
|
CGGGAGA | C | 4 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136others(1): Show | 5 | NA18964.hp1 NA18970.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+38201_99+38206d others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109598617 | |||||
| chr4:109598624
|
G | C | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+38188G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598624 | ||||||
| chr4:109598625
|
G | C | 1 | a0003c0003t0001g0286 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.99+38189G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598625 | ||||||
| chr4:109598631
|
G | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.99+38195G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598631 | ||||||
| chr4:109598656
|
C | A | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+38220C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598656 | ||||||
| chr4:109598682
|
T | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+38246T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598682 | ||||||
| chr4:109598809
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+38373A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598809 | ||||||
| chr4:109598869
|
A | G | 5 | a0003c0003t0001g0025a0003c0003t0001g0027a0003c0003t0001g0155others(2): Show | 5 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+38433A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598869 | ||||||
| chr4:109599172
|
C | T | 19 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00639.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+38736C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599172 | ||||||
| chr4:109599204
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+38768T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599204 | ||||||
| chr4:109599355
|
G | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+38919G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599355 | ||||||
| chr4:109599386
|
C | T | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+38950C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599386 | ||||||
| chr4:109599422
|
AT | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+38993delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109599422 | |||||
| chr4:109599575
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+39139A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599575 | ||||||
| chr4:109599592
|
T | C | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+39156T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599592 | ||||||
| chr4:109599661
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99+39225A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599661 | ||||||
| chr4:109599676
|
TA | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0290a0003c0003t0001g0004others(2): Show | 6 | HG00639.hp2 NA18995.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+39241delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599676 | ||||||
| chr4:109599677
|
A | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(155): Show | 160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.99+39241A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599677 | ||||||
| chr4:109599678
|
T | TA | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+39242_99+39243i others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599678 | ||||||
| chr4:109599680
|
TA | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+39245delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599680 | ||||||
| chr4:109599681
|
A | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.99+39245A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599681 | ||||||
| chr4:109599681
|
AT | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+39252delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109599681 | |||||
| chr4:109599715
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+39279G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599715 | ||||||
| chr4:109599795
|
A | G | 49 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+39359A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599795 | ||||||
| chr4:109599913
|
G | A | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+39477G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599913 | ||||||
| chr4:109600172
|
A | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+39736A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600172 | ||||||
| chr4:109600213
|
C | T | 11 | a0001c0001t0001g0089a0001c0001t0003g0076a0001c0001t0003g0079others(8): Show | 11 | HG02080.hp2 HG02165.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+39777C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600213 | ||||||
| chr4:109600303
|
G | T | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+39867G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600303 | ||||||
| chr4:109600494
|
A | G | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+40058A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600494 | ||||||
| chr4:109600571
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+40135T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600571 | ||||||
| chr4:109600679
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+40243C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600679 | ||||||
| chr4:109600800
|
A | T | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+40364A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600800 | ||||||
| chr4:109600856
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+40420A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600856 | ||||||
| chr4:109601108
|
TA | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.99+40680delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109601108 | |||||
| chr4:109601151
|
G | A | 3 | a0001c0001t0004g0055a0003c0003t0001g0053a0003c0003t0001g0054 | 3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.99+40715G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601151 | ||||||
| chr4:109601321
|
C | G | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+40885C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601321 | ||||||
| chr4:109601342
|
T | G | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+40906T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601342 | ||||||
| chr4:109601359
|
G | A | 6 | a0003c0003t0001g0084a0003c0003t0001g0240a0003c0003t0001g0242others(3): Show | 6 | HG00544.hp1 HG02135.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+40923G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601359 | ||||||
| chr4:109601422
|
A | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0044 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.99+40986A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601422 | ||||||
| chr4:109601431
|
C | CT | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(2): Show | 5 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+40998dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109601431 | |||||
| chr4:109601605
|
T | C | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+41169T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601605 | ||||||
| chr4:109601635
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+41199T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601635 | ||||||
| chr4:109601888
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+41452A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601888 | ||||||
| chr4:109602325
|
T | C | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+41889T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602325 | ||||||
| chr4:109602448
|
G | T | 1 | a0004c0004t0001g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+42012G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602448 | ||||||
| chr4:109602681
|
C | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+42245C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602681 | ||||||
| chr4:109602695
|
T | C | 1 | a0002c0002t0002g0322 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.99+42259T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602695 | ||||||
| chr4:109602856
|
T | C | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+42420T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602856 | ||||||
| chr4:109603040
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+42604C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603040 | ||||||
| chr4:109603089
|
C | T | 1 | a0005c0009t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+42653C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603089 | ||||||
| chr4:109603122
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+42686C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603122 | ||||||
| chr4:109603148
|
C | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+42712C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603148 | ||||||
| chr4:109603219
|
C | T | 7 | a0001c0001t0001g0280a0001c0001t0002g0327a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+42783C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603219 | ||||||
| chr4:109603220
|
CGAGTGCC others(4): Show |
C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+42785_99+42795d others(13): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603220 | ||||||
| chr4:109603225
|
G | A | 5 | a0003c0003t0001g0179a0003c0003t0001g0180a0003c0003t0001g0245others(2): Show | 5 | HG01928.hp1 HG01943.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+42789G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603225 | ||||||
| chr4:109603241
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+42805G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603241 | ||||||
| chr4:109603252
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+42816C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603252 | ||||||
| chr4:109603261
|
G | T | 1 | a0001c0012t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99+42825G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603261 | ||||||
| chr4:109603305
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0039 | 3 | HG02258.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.99+42869C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603305 | ||||||
| chr4:109603314
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.99+42878C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603314 | ||||||
| chr4:109603318
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+42882G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603318 | ||||||
| chr4:109603328
|
C | T | 49 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0111others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+42892C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603328 | ||||||
| chr4:109603352
|
C | T | 5 | a0003c0003t0001g0230a0003c0003t0001g0246a0003c0003t0001g0303others(2): Show | 5 | NA18946.hp1 NA18975.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+42916C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603352 | ||||||
| chr4:109603499
|
G | T | 1 | a0002c0002t0002g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+43063G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603499 | ||||||
| chr4:109603521
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+43085G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603521 | ||||||
| chr4:109603583
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43147T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603583 | ||||||
| chr4:109603592
|
G | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43156G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603592 | ||||||
| chr4:109603628
|
G | A | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+43192G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603628 | ||||||
| chr4:109603667
|
C | A | 4 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0059others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43231C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603667 | ||||||
| chr4:109603667
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+43231C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603667 | ||||||
| chr4:109603668
|
G | A | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+43232G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603668 | ||||||
| chr4:109603680
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43244G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603680 | ||||||
| chr4:109603698
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(10): Show | 14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+43262G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603698 | ||||||
| chr4:109603740
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+43304C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603740 | ||||||
| chr4:109603744
|
C | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.99+43308C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603744 | ||||||
| chr4:109603744
|
C | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(161): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.99+43308C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603744 | ||||||
| chr4:109603784
|
C | T | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+43348C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603784 | ||||||
| chr4:109603825
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43389G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603825 | ||||||
| chr4:109603829
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43393A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603829 | ||||||
| chr4:109603869
|
A | AC | 23 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0060others(20): Show | 23 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+43437dupC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109603869 | |||||
| chr4:109603873
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43437C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603873 | ||||||
| chr4:109603874
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+43438G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603874 | ||||||
| chr4:109603907
|
C | T | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+43471C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603907 | ||||||
| chr4:109603908
|
G | A | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+43472G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603908 | ||||||
| chr4:109604095
|
G | A | 1 | a0001c0001t0001g0323 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.99+43659G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604095 | ||||||
| chr4:109604137
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+43701G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604137 | ||||||
| chr4:109604172
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+43736G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604172 | ||||||
| chr4:109604177
|
T | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43741T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604177 | ||||||
| chr4:109604207
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+43771A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604207 | ||||||
| chr4:109604299
|
G | GGTTA | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43863_99+43864i others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604299 | ||||||
| chr4:109604299
|
G | GTTTA | 169 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(166): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.99+43864_99+43865i others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109604299 | |||||
| chr4:109604310
|
C | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43874C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604310 | ||||||
| chr4:109604329
|
G | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+43893G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604329 | ||||||
| chr4:109604395
|
A | T | 14 | a0001c0001t0001g0049a0001c0001t0003g0167a0001c0001t0003g0231others(11): Show | 14 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+43959A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604395 | ||||||
| chr4:109604445
|
AATC | A | 3 | a0003c0003t0001g0244a0003c0003t0001g0262a0003c0003t0001g0270 | 3 | HG02165.hp1 NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.99+44012_99+44014d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109604445 | |||||
| chr4:109604543
|
A | G | 1 | a0003c0003t0001g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.99+44107A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604543 | ||||||
| chr4:109604569
|
T | G | 3 | a0002c0002t0002g0007a0002c0002t0002g0199a0002c0002t0002g0206 | 3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.99+44133T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604569 | ||||||
| chr4:109604588
|
C | T | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+44152C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604588 | ||||||
| chr4:109604623
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+44187G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604623 | ||||||
| chr4:109604640
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+44204T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604640 | ||||||
| chr4:109604683
|
A | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+44247A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604683 | ||||||
| chr4:109604846
|
A | G | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+44410A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604846 | ||||||
| chr4:109605017
|
G | T | 3 | a0003c0003t0001g0230a0003c0003t0001g0303a0003c0003t0001g0304 | 3 | NA18992.hp2 NA18994.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.99+44581G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605017 | ||||||
| chr4:109605165
|
TTGGC | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+44733_99+44736d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605165 | |||||
| chr4:109605291
|
G | A | 7 | a0001c0001t0001g0280a0001c0001t0002g0327a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+44855G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605291 | ||||||
| chr4:109605323
|
G | GT | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+44888dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605323 | |||||
| chr4:109605355
|
A | G | 5 | a0003c0003t0001g0179a0003c0003t0001g0180a0003c0003t0001g0245others(2): Show | 5 | HG01928.hp1 HG01943.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+44919A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605355 | ||||||
| chr4:109605457
|
A | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0295 | 3 | HG00642.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.99+45021A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605457 | ||||||
| chr4:109605474
|
A | G | 1 | a0003c0003t0001g0164 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+45038A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605474 | ||||||
| chr4:109605493
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.99+45057G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605493 | ||||||
| chr4:109605657
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.99+45221G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605657 | ||||||
| chr4:109605696
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+45260A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605696 | ||||||
| chr4:109605799
|
T | C | 1 | a0007c0010t0001g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.99+45363T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605799 | ||||||
| chr4:109605829
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0047 | 3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+45393C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605829 | ||||||
| chr4:109605854
|
G | A | 9 | a0001c0001t0001g0068a0004c0004t0001g0013a0004c0004t0001g0028others(6): Show | 9 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+45418G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605854 | ||||||
| chr4:109605958
|
T | TTTTG | 5 | a0001c0001t0001g0006a0001c0006t0005g0002a0001c0006t0005g0128others(2): Show | 6 | HG03516.hp1 NA18964.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+45550_99+45553d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605958 | |||||
| chr4:109605958
|
TTTTGTTT others(1): Show |
T | 167 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.99+45546_99+45553d others(10): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605958 | |||||
| chr4:109605964
|
T | G | 1 | a0001c0001t0005g0095 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+45528T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605964 | ||||||
| chr4:109605978
|
G | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+45542G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605978 | ||||||
| chr4:109605999
|
G | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(17): Show | 20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+45563G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605999 | ||||||
| chr4:109606049
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+45613G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606049 | ||||||
| chr4:109606132
|
G | A | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.99+45696G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606132 | ||||||
| chr4:109606257
|
G | GA | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+45822dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606257 | |||||
| chr4:109606276
|
G | GT | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+45848dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606276 | |||||
| chr4:109606276
|
GT | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+45848delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606276 | |||||
| chr4:109606551
|
C | T | 3 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0295 | 3 | HG00642.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.99+46115C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606551 | ||||||
| chr4:109606698
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+46262T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606698 | ||||||
| chr4:109606754
|
TTG | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+46327_99+46328d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606754 | |||||
| chr4:109606780
|
C | G | 16 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+46344C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606780 | ||||||
| chr4:109606848
|
G | A | 1 | a0001c0001t0005g0095 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+46412G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606848 | ||||||
| chr4:109606906
|
C | T | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+46470C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606906 | ||||||
| chr4:109607141
|
G | GT | 17 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+46705_99+46706i others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607141 | ||||||
| chr4:109607142
|
A | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+46706A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607142 | ||||||
| chr4:109607160
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+46724C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607160 | ||||||
| chr4:109607209
|
TTTTC | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.99+46793_99+46796d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109607209 | |||||
| chr4:109607374
|
C | T | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+46938C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607374 | ||||||
| chr4:109607378
|
C | A | 4 | a0002c0002t0002g0100a0002c0002t0002g0205a0002c0002t0002g0214others(1): Show | 4 | HG00621.hp2 NA18949.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+46942C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607378 | ||||||
| chr4:109607401
|
A | G | 1 | a0004c0004t0001g0252 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+46965A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607401 | ||||||
| chr4:109607461
|
G | T | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+47025G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607461 | ||||||
| chr4:109607668
|
G | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067 | 3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+47232G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607668 | ||||||
| chr4:109607770
|
C | T | 1 | a0002c0002t0002g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99+47334C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607770 | ||||||
| chr4:109607786
|
G | T | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+47350G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607786 | ||||||
| chr4:109607804
|
C | G | 6 | a0002c0002t0002g0278a0003c0003t0001g0219a0003c0003t0001g0286others(3): Show | 6 | HG00423.hp1 HG02155.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+47368C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607804 | ||||||
| chr4:109607840
|
A | G | 2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG02523.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.99+47404A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607840 | ||||||
| chr4:109607868
|
T | C | 70 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+47432T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607868 | ||||||
| chr4:109607868
|
T | G | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+47432T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607868 | ||||||
| chr4:109607909
|
T | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+47473T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607909 | ||||||
| chr4:109608048
|
T | A | 2 | a0002c0002t0002g0205a0002c0002t0002g0214 | 2 | NA18949.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.99+47612T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608048 | ||||||
| chr4:109608081
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+47645T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608081 | ||||||
| chr4:109608187
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067 | 3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+47751C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608187 | ||||||
| chr4:109608343
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.99+47907A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608343 | ||||||
| chr4:109608358
|
GT | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+47923delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608358 | ||||||
| chr4:109608365
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+47929A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608365 | ||||||
| chr4:109608390
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.99+47954C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608390 | ||||||
| chr4:109608473
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+48037G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608473 | ||||||
| chr4:109608485
|
G | GGTTTT | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+48066_99+48070d others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109608485 | |||||
| chr4:109608530
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.99+48094C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608530 | ||||||
| chr4:109608702
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+48266C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608702 | ||||||
| chr4:109608797
|
G | A | 3 | a0002c0002t0002g0130a0002c0002t0002g0157a0002c0002t0002g0215 | 3 | HG00741.hp2 HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.99+48361G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608797 | ||||||
| chr4:109608812
|
G | T | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+48376G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608812 | ||||||
| chr4:109608857
|
T | A | 1 | a0002c0002t0002g0153 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.99+48421T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608857 | ||||||
| chr4:109609041
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.99+48605T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609041 | ||||||
| chr4:109609065
|
ATC | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.99+48645_99+48646d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109609065 | |||||
| chr4:109609065
|
ATCTCTC | A | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+48641_99+48646d others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109609065 | |||||
| chr4:109609081
|
CTG | C | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+48648_99+48649d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109609081 | |||||
| chr4:109609142
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+48706A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609142 | ||||||
| chr4:109609185
|
T | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+48749T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609185 | ||||||
| chr4:109609250
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.99+48814G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609250 | ||||||
| chr4:109609302
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+48866A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609302 | ||||||
| chr4:109609627
|
C | G | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0001t0004g0058others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+49191C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609627 | ||||||
| chr4:109609758
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.100-49253G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609758 | ||||||
| chr4:109609805
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(249): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.100-49206A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609805 | ||||||
| chr4:109609848
|
C | T | 2 | a0002c0002t0002g0311a0003c0003t0007g0005 | 3 | HG01255.hp2 HG01358.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.100-49163C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609848 | ||||||
| chr4:109609887
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100-49124G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609887 | ||||||
| chr4:109610060
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-48951T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610060 | ||||||
| chr4:109610086
|
T | C | 3 | a0003c0003t0001g0230a0003c0003t0001g0303a0003c0003t0001g0304 | 3 | NA18992.hp2 NA18994.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.100-48925T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610086 | ||||||
| chr4:109610179
|
C | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-48832C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610179 | ||||||
| chr4:109610195
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.100-48816T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610195 | ||||||
| chr4:109610276
|
C | T | 4 | a0002c0002t0002g0114a0002c0002t0002g0146a0002c0002t0002g0147others(1): Show | 4 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-48735C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610276 | ||||||
| chr4:109610317
|
T | G | 1 | a0002c0002t0002g0149 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.100-48694T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610317 | ||||||
| chr4:109610349
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-48662G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610349 | ||||||
| chr4:109610367
|
G | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-48644G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610367 | ||||||
| chr4:109610412
|
A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(10): Show | 14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-48599A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610412 | ||||||
| chr4:109610485
|
A | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-48526A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610485 | ||||||
| chr4:109610487
|
A | G | 10 | a0001c0001t0001g0049a0001c0001t0001g0068a0004c0004t0001g0013others(7): Show | 10 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-48524A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610487 | ||||||
| chr4:109610643
|
T | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-48368T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610643 | ||||||
| chr4:109610661
|
A | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-48350A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610661 | ||||||
| chr4:109610768
|
A | T | 2 | a0001c0001t0001g0006a0004c0004t0001g0331 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-48243A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610768 | ||||||
| chr4:109610970
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.100-48041T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610970 | ||||||
| chr4:109611063
|
AAAGAGAG others(30): Show |
A | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067 | 3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-47943_100-4790 others(41): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109611063 | |||||
| chr4:109611429
|
G | A | 1 | a0003c0003t0001g0272 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.100-47582G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611429 | ||||||
| chr4:109611450
|
T | A | 1 | a0003c0003t0001g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-47561T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611450 | ||||||
| chr4:109611451
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-47560G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611451 | ||||||
| chr4:109611461
|
C | G | 2 | a0001c0001t0001g0068a0004c0004t0001g0035 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-47550C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611461 | ||||||
| chr4:109611674
|
T | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(10): Show | 14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-47337T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611674 | ||||||
| chr4:109611707
|
T | C | 2 | a0003c0003t0001g0260a0003c0003t0001g0265 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.100-47304T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611707 | ||||||
| chr4:109611751
|
T | C | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-47260T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611751 | ||||||
| chr4:109612107
|
C | A | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100-46904C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612107 | ||||||
| chr4:109612181
|
G | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067 | 3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-46830G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612181 | ||||||
| chr4:109612197
|
C | T | 1 | a0001c0001t0005g0222 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.100-46814C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612197 | ||||||
| chr4:109612243
|
T | TTC | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067 | 3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-46766_100-4676 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612243 | |||||
| chr4:109612263
|
C | CT | 177 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0061others(174): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.100-46729dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612263 | |||||
| chr4:109612263
|
C | CTT | 35 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(32): Show | 36 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-46730_100-4672 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612263 | |||||
| chr4:109612263
|
C | CTTT | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00639.hp1 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-46731_100-4672 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612263 | |||||
| chr4:109612267
|
T | TC | 3 | a0001c0001t0001g0134a0001c0001t0001g0239a0003c0003t0001g0266 | 3 | HG01071.hp1 NA19012.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.100-46744_100-4674 others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612267 | ||||||
| chr4:109612288
|
C | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.100-46723C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612288 | ||||||
| chr4:109612340
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-46671C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612340 | ||||||
| chr4:109612356
|
T | C | 2 | a0001c0001t0001g0061a0001c0012t0001g0051 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-46655T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612356 | ||||||
| chr4:109612379
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100-46632A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612379 | ||||||
| chr4:109612415
|
T | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 31 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-46596T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612415 | ||||||
| chr4:109612419
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-46592A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612419 | ||||||
| chr4:109612517
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0062others(147): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.100-46494C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612517 | ||||||
| chr4:109612594
|
C | A | 1 | a0004c0004t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-46417C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612594 | ||||||
| chr4:109612770
|
G | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-46241G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612770 | ||||||
| chr4:109612792
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100-46219C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612792 | ||||||
| chr4:109612832
|
T | C | 1 | a0001c0001t0005g0195 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-46179T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612832 | ||||||
| chr4:109612835
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.100-46176G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612835 | ||||||
| chr4:109612835
|
G | T | 1 | a0003c0003t0001g0313 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.100-46176G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612835 | ||||||
| chr4:109612839
|
T | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0048others(4): Show | 7 | HG01168.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-46172T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612839 | ||||||
| chr4:109612852
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0213a0001c0001t0001g0323 | 3 | NA18940.hp1 NA18954.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.100-46159A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612852 | ||||||
| chr4:109612854
|
C | T | 1 | a0002c0002t0002g0322 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-46157C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612854 | ||||||
| chr4:109612877
|
C | A | 1 | a0005c0009t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-46134C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612877 | ||||||
| chr4:109612882
|
G | A | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-46129G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612882 | ||||||
| chr4:109612889
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.100-46122A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612889 | ||||||
| chr4:109612897
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.100-46114G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612897 | ||||||
| chr4:109612902
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100-46109C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612902 | ||||||
| chr4:109612903
|
A | G | 25 | a0001c0001t0001g0061a0001c0001t0003g0123a0001c0001t0003g0194others(22): Show | 25 | HG00438.hp1 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-46108A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612903 | ||||||
| chr4:109612917
|
T | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0060others(50): Show | 53 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-46094T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612917 | ||||||
| chr4:109612922
|
C | T | 8 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-46089C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612922 | ||||||
| chr4:109612930
|
T | C | 8 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-46081T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612930 | ||||||
| chr4:109612933
|
C | T | 8 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-46078C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612933 | ||||||
| chr4:109612974
|
C | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0171a0002c0002t0002g0092others(2): Show | 5 | HG02040.hp2 HG02071.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-46037C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612974 | ||||||
| chr4:109612976
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-46035G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612976 | ||||||
| chr4:109612980
|
T | C | 1 | a0003c0003t0001g0281 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-46031T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612980 | ||||||
| chr4:109612993
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.100-46018C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612993 | ||||||
| chr4:109612999
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0005g0099a0001c0001t0005g0171others(4): Show | 7 | HG00735.hp2 HG02040.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-46012G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612999 | ||||||
| chr4:109613028
|
C | T | 4 | a0002c0002t0002g0114a0002c0002t0002g0146a0002c0002t0002g0147others(1): Show | 4 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-45983C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613028 | ||||||
| chr4:109613030
|
C | T | 1 | a0003c0003t0001g0310 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100-45981C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613030 | ||||||
| chr4:109613300
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-45711T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613300 | ||||||
| chr4:109613330
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-45681G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613330 | ||||||
| chr4:109613333
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-45678C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613333 | ||||||
| chr4:109613398
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100-45613A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613398 | ||||||
| chr4:109613425
|
G | T | 1 | a0004c0004t0001g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-45586G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613425 | ||||||
| chr4:109613550
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100-45461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613550 | ||||||
| chr4:109613637
|
C | T | 75 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0005t0002g0253others(72): Show | 77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-45374C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613637 | ||||||
| chr4:109613660
|
C | A | 1 | a0001c0001t0003g0011 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100-45351C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613660 | ||||||
| chr4:109613853
|
C | CTA | 250 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(247): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.100-45157_100-4515 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109613853 | |||||
| chr4:109614156
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100-44855C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614156 | ||||||
| chr4:109614261
|
CAG | C | 33 | a0001c0001t0001g0089a0001c0001t0003g0003a0001c0001t0003g0011others(30): Show | 34 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.100-44747_100-4474 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109614261 | |||||
| chr4:109614296
|
G | A | 3 | a0002c0002t0002g0121a0002c0002t0002g0124a0002c0002t0002g0212 | 3 | HG01081.hp2 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.100-44715G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614296 | ||||||
| chr4:109614431
|
A | C | 1 | a0001c0001t0005g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-44580A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614431 | ||||||
| chr4:109614432
|
C | T | 166 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0068others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.100-44579C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614432 | ||||||
| chr4:109614501
|
C | T | 1 | a0001c0012t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.100-44510C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614501 | ||||||
| chr4:109614642
|
G | A | 1 | a0001c0005t0006g0008 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-44369G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614642 | ||||||
| chr4:109614720
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 20 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-44291G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614720 | ||||||
| chr4:109614778
|
G | A | 3 | a0003c0003t0001g0261a0003c0003t0001g0277a0003c0003t0001g0312 | 3 | HG01257.hp2 HG01891.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.100-44233G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614778 | ||||||
| chr4:109614915
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-44096C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614915 | ||||||
| chr4:109615260
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43751C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615260 | ||||||
| chr4:109615272
|
T | C | 4 | a0001c0001t0002g0327a0001c0005t0006g0046a0001c0005t0006g0169others(1): Show | 4 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-43739T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615272 | ||||||
| chr4:109615336
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-43675C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615336 | ||||||
| chr4:109615405
|
A | AT | 32 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.100-43588dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109615405 | |||||
| chr4:109615417
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43594T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615417 | ||||||
| chr4:109615428
|
C | T | 4 | a0001c0001t0001g0118a0001c0001t0001g0172a0001c0001t0001g0174others(1): Show | 4 | HG01070.hp1 HG01433.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43583C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615428 | ||||||
| chr4:109615490
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-43521C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615490 | ||||||
| chr4:109615531
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-43480C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615531 | ||||||
| chr4:109615532
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(245): Show | 253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.100-43479A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615532 | ||||||
| chr4:109615568
|
C | T | 75 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0089others(72): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.100-43443C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615568 | ||||||
| chr4:109615630
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43381C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615630 | ||||||
| chr4:109615652
|
G | A | 1 | a0003c0003t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.100-43359G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615652 | ||||||
| chr4:109616095
|
T | C | 2 | a0001c0001t0004g0227a0001c0001t0004g0297 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.100-42916T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616095 | ||||||
| chr4:109616222
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067 | 3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-42789C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616222 | ||||||
| chr4:109616274
|
CATTTT | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.100-42730_100-4272 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109616274 | |||||
| chr4:109616317
|
T | C | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-42694T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616317 | ||||||
| chr4:109616411
|
A | G | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0005t0002g0253others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-42600A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616411 | ||||||
| chr4:109616523
|
C | A | 1 | a0001c0005t0006g0008 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-42488C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616523 | ||||||
| chr4:109616569
|
T | A | 1 | a0005c0009t0001g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-42442T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616569 | ||||||
| chr4:109616620
|
A | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-42391A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616620 | ||||||
| chr4:109616693
|
A | C | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0005t0002g0253others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-42318A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616693 | ||||||
| chr4:109616770
|
A | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-42241A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616770 | ||||||
| chr4:109616827
|
G | GCCCT | 4 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0236others(1): Show | 5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-42182_100-4217 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109616827 | |||||
| chr4:109617051
|
AACC | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0089others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.100-41958_100-4195 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109617051 | |||||
| chr4:109617153
|
C | G | 1 | a0001c0001t0005g0171 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.100-41858C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617153 | ||||||
| chr4:109617183
|
G | A | 2 | a0002c0002t0002g0141a0002c0002t0002g0203 | 2 | NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.100-41828G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617183 | ||||||
| chr4:109617188
|
A | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0089others(147): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.100-41823A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617188 | ||||||
| chr4:109617243
|
G | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-41768G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617243 | ||||||
| chr4:109617273
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.100-41738A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617273 | ||||||
| chr4:109617318
|
T | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-41693T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617318 | ||||||
| chr4:109617347
|
G | A | 3 | a0003c0003t0001g0257a0003c0003t0001g0258a0003c0003t0001g0259 | 3 | HG02129.hp2 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.100-41664G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617347 | ||||||
| chr4:109617416
|
C | T | 4 | a0004c0004t0001g0228a0004c0004t0001g0251a0004c0004t0001g0252others(1): Show | 4 | HG02145.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-41595C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617416 | ||||||
| chr4:109617603
|
G | A | 150 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0089others(147): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.100-41408G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617603 | ||||||
| chr4:109617710
|
A | G | 3 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0002t0002g0074 | 3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100-41301A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617710 | ||||||
| chr4:109617846
|
T | C | 150 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0089others(147): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.100-41165T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617846 | ||||||
| chr4:109617965
|
T | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-41046T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617965 | ||||||
| chr4:109618018
|
C | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-40993C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618018 | ||||||
| chr4:109618286
|
A | G | 83 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0062others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.100-40725A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618286 | ||||||
| chr4:109618501
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100-40510C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618501 | ||||||
| chr4:109618506
|
C | G | 1 | a0001c0001t0003g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-40505C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618506 | ||||||
| chr4:109618579
|
A | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-40432A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618579 | ||||||
| chr4:109618624
|
A | C | 1 | a0003c0003t0001g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.100-40387A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618624 | ||||||
| chr4:109618768
|
T | TA | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0005t0002g0253others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-40242dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618768 | |||||
| chr4:109618880
|
C | G | 3 | a0002c0002t0002g0114a0002c0002t0002g0147a0002c0002t0002g0162 | 3 | HG01070.hp2 HG01071.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.100-40131C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618880 | ||||||
| chr4:109618952
|
T | TTC | 38 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0029others(35): Show | 38 | HG01243.hp1 HG01346.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-40023_100-4002 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTC | 7 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0003g0232others(4): Show | 7 | HG02129.hp2 HG02258.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-40025_100-4002 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTC | 6 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-40027_100-4002 others(10): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(1): Show |
3 | a0001c0001t0004g0018a0001c0001t0004g0021a0003c0003t0001g0296 | 3 | HG02738.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.100-40029_100-4002 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(3): Show |
1 | a0003c0003t0007g0005 | 2 | HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.100-40031_100-4002 others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(5): Show |
5 | a0001c0001t0001g0017a0001c0001t0004g0019a0001c0001t0004g0022others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-40033_100-4002 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(7): Show |
3 | a0001c0001t0004g0016a0001c0001t0004g0020a0001c0001t0004g0024 | 3 | HG02622.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.100-40035_100-4002 others(18): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(11): Show |
1 | a0001c0006t0005g0002 | 2 | NA18970.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.100-40039_100-4002 others(22): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(13): Show |
1 | a0001c0006t0005g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-40041_100-4002 others(24): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
T | TTCTCTCT others(17): Show |
1 | a0001c0006t0005g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.100-40045_100-4002 others(28): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
TTC | T | 88 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(85): Show | 88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.100-40023_100-4002 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
TTCTC | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0048others(19): Show | 22 | HG00423.hp1 HG01109.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-40025_100-4002 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
TTCTCTCT others(1): Show |
T | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-40029_100-4002 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618952
|
TTCTCTCT others(3): Show |
T | 1 | a0001c0001t0001g0300 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100-40031_100-4002 others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | |||||
| chr4:109618983
|
T | TCTCTCTA others(1): Show |
3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-40025_100-4001 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618983 | |||||
| chr4:109618986
|
C | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-40025C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618986 | ||||||
| chr4:109618987
|
T | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-40024T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618987 | ||||||
| chr4:109618993
|
T | A | 7 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-40018T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618993 | ||||||
| chr4:109618997
|
A | AACCT | 14 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-39996_100-3999 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618997 | |||||
| chr4:109618997
|
A | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-40014A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618997 | ||||||
| chr4:109619019
|
T | C | 1 | a0001c0001t0005g0195 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-39992T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619019 | ||||||
| chr4:109619022
|
A | ACCTG | 25 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0184others(22): Show | 26 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-39981_100-3997 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619022 | |||||
| chr4:109619022
|
A | ACCTGCCT others(1): Show |
59 | a0001c0001t0001g0256a0001c0005t0002g0253a0002c0002t0002g0090others(56): Show | 61 | HG00280.hp1 HG00423.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-39985_100-3997 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619022 | |||||
| chr4:109619022
|
A | ACCTGCCT others(9): Show |
13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00621.hp1 HG02040.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-39978_100-3997 others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619022 | |||||
| chr4:109619022
|
A | ATCTACCT others(13): Show |
1 | a0001c0001t0005g0195 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-39989_100-3998 others(24): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619022 | ||||||
| chr4:109619026
|
GCCTGCCT others(1): Show |
G | 30 | a0001c0001t0001g0061a0001c0001t0003g0003a0001c0001t0003g0011others(27): Show | 31 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-39981_100-3997 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619026 | |||||
| chr4:109619026
|
GCCTGCCT others(5): Show |
G | 2 | a0001c0001t0003g0209a0001c0012t0001g0051 | 2 | HG01255.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.100-39981_100-3997 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619026 | |||||
| chr4:109619026
|
GCCTGCCT others(9): Show |
G | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-39981_100-3996 others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619026 | |||||
| chr4:109619030
|
G | GCCTA | 10 | a0001c0005t0006g0008a0002c0002t0002g0109a0002c0002t0002g0110others(7): Show | 10 | HG00544.hp2 HG01346.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-39936_100-3993 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619030
|
G | GCCTACCT others(1): Show |
6 | a0002c0002t0002g0129a0002c0002t0002g0154a0002c0002t0002g0159others(3): Show | 6 | HG01168.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-39940_100-3993 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619030
|
G | GCCTGCCT others(5): Show |
7 | a0003c0003t0001g0179a0003c0003t0001g0180a0003c0003t0001g0230others(4): Show | 7 | HG03492.hp1 HG03654.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-39978_100-3997 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619030
|
G | GCCTGCCT others(9): Show |
3 | a0003c0003t0001g0270a0003c0003t0001g0318a0003c0003t0001g0319 | 3 | HG02165.hp1 NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.100-39978_100-3997 others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619030
|
GCCTA | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0052others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-39936_100-3993 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619030
|
GCCTACCT others(5): Show |
G | 4 | a0001c0001t0001g0014a0001c0001t0001g0071a0002c0002t0002g0205others(1): Show | 4 | HG00639.hp1 HG02818.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-39944_100-3993 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619030
|
GCCTACCT others(13): Show |
G | 1 | a0001c0001t0004g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-39952_100-3993 others(24): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | |||||
| chr4:109619034
|
A | G | 97 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0089others(94): Show | 97 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.100-39977A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619034 | ||||||
| chr4:109619038
|
A | G | 17 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0106others(14): Show | 17 | HG00280.hp2 HG00438.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-39973A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619038 | ||||||
| chr4:109619042
|
A | G | 1 | a0001c0001t0005g0223 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-39969A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619042 | ||||||
| chr4:109619046
|
A | G | 1 | a0001c0001t0005g0223 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-39965A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619046 | ||||||
| chr4:109619050
|
A | G | 1 | a0001c0001t0005g0223 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-39961A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619050 | ||||||
| chr4:109619054
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-39957A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619054 | ||||||
| chr4:109619089
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-39922T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619089 | ||||||
| chr4:109619170
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-39841G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619170 | ||||||
| chr4:109619298
|
C | T | 74 | a0001c0001t0001g0256a0001c0001t0003g0069a0001c0005t0002g0253others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-39713C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619298 | ||||||
| chr4:109619326
|
G | A | 153 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.100-39685G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619326 | ||||||
| chr4:109619395
|
A | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-39616A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619395 | ||||||
| chr4:109619576
|
G | A | 44 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0106others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-39435G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619576 | ||||||
| chr4:109619824
|
A | G | 25 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0004g0016others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.100-39187A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619824 | ||||||
| chr4:109619954
|
A | C | 153 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.100-39057A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619954 | ||||||
| chr4:109619955
|
C | A | 153 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.100-39056C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619955 | ||||||
| chr4:109619961
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-39050T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619961 | ||||||
| chr4:109619962
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-39049A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619962 | ||||||
| chr4:109620052
|
A | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-38959A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620052 | ||||||
| chr4:109620076
|
C | T | 153 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.100-38935C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620076 | ||||||
| chr4:109620175
|
A | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-38836A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620175 | ||||||
| chr4:109620238
|
A | T | 1 | a0003c0003t0001g0281 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-38773A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620238 | ||||||
| chr4:109620428
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0209 | 2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.100-38583G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620428 | ||||||
| chr4:109620580
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-38431C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620580 | ||||||
| chr4:109620684
|
A | C | 153 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.100-38327A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620684 | ||||||
| chr4:109620899
|
C | CT | 167 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(164): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.100-38100dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109620899 | |||||
| chr4:109620911
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100-38100T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620911 | ||||||
| chr4:109621060
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-37951G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621060 | ||||||
| chr4:109621180
|
T | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-37831T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621180 | ||||||
| chr4:109621361
|
G | C | 1 | a0004c0004t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-37650G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621361 | ||||||
| chr4:109621558
|
A | G | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-37453A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621558 | ||||||
| chr4:109621588
|
A | G | 1 | a0003c0003t0001g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-37423A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621588 | ||||||
| chr4:109621668
|
T | C | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-37343T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621668 | ||||||
| chr4:109621767
|
A | C | 1 | a0001c0001t0005g0095 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.100-37244A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621767 | ||||||
| chr4:109622031
|
G | A | 79 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0068others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.100-36980G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622031 | ||||||
| chr4:109622134
|
G | T | 10 | a0001c0001t0001g0068a0004c0004t0001g0013a0004c0004t0001g0028others(7): Show | 10 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-36877G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622134 | ||||||
| chr4:109622219
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-36792A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622219 | ||||||
| chr4:109622522
|
A | C | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-36489A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622522 | ||||||
| chr4:109622668
|
T | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-36343T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622668 | ||||||
| chr4:109622694
|
A | G | 1 | a0003c0003t0001g0272 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.100-36317A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622694 | ||||||
| chr4:109622787
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-36224C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622787 | ||||||
| chr4:109622852
|
G | A | 1 | a0002c0002t0002g0159 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100-36159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622852 | ||||||
| chr4:109622888
|
C | G | 3 | a0003c0003t0001g0261a0003c0003t0001g0277a0003c0003t0001g0312 | 3 | HG01257.hp2 HG01891.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.100-36123C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622888 | ||||||
| chr4:109622945
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-36066G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622945 | ||||||
| chr4:109623127
|
A | C | 32 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0036others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-35884A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623127 | ||||||
| chr4:109623210
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-35801G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623210 | ||||||
| chr4:109623215
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-35796G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623215 | ||||||
| chr4:109623412
|
A | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-35599A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623412 | ||||||
| chr4:109623439
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-35572T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623439 | ||||||
| chr4:109623479
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(10): Show | 14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-35532T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623479 | ||||||
| chr4:109623511
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-35500C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623511 | ||||||
| chr4:109623540
|
C | T | 151 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0089others(148): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.100-35471C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623540 | ||||||
| chr4:109623595
|
G | T | 1 | a0002c0002t0002g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-35416G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623595 | ||||||
| chr4:109623687
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-35324A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623687 | ||||||
| chr4:109623776
|
G | A | 3 | a0001c0001t0003g0069a0001c0001t0003g0079a0001c0001t0003g0081 | 3 | HG02165.hp2 HG03710.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.100-35235G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623776 | ||||||
| chr4:109623800
|
C | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(244): Show | 252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.100-35211C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623800 | ||||||
| chr4:109624072
|
T | C | 170 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0089others(167): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.100-34939T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624072 | ||||||
| chr4:109624284
|
T | G | 1 | a0002c0002t0002g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-34727T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624284 | ||||||
| chr4:109624291
|
A | G | 5 | a0003c0003t0001g0025a0003c0003t0001g0027a0003c0003t0001g0155others(2): Show | 5 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-34720A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624291 | ||||||
| chr4:109624322
|
C | T | 3 | a0001c0001t0004g0055a0003c0003t0001g0053a0003c0003t0001g0054 | 3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-34689C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624322 | ||||||
| chr4:109624327
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-34684G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624327 | ||||||
| chr4:109624376
|
T | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-34635T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624376 | ||||||
| chr4:109624459
|
G | A | 1 | a0002c0002t0002g0254 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.100-34552G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624459 | ||||||
| chr4:109624628
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-34383G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624628 | ||||||
| chr4:109624848
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0331 | 3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-34163A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624848 | ||||||
| chr4:109624863
|
A | T | 2 | a0001c0001t0001g0048a0004c0004t0001g0331 | 2 | HG00735.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.100-34148A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624863 | ||||||
| chr4:109624967
|
C | T | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.100-34044C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624967 | ||||||
| chr4:109625012
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(245): Show | 253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.100-33999T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625012 | ||||||
| chr4:109625133
|
C | T | 4 | a0002c0002t0002g0117a0002c0002t0002g0145a0002c0002t0002g0208others(1): Show | 4 | HG00099.hp1 HG01175.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-33878C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625133 | ||||||
| chr4:109625142
|
A | G | 1 | a0004c0004t0001g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-33869A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625142 | ||||||
| chr4:109625227
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-33784C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625227 | ||||||
| chr4:109625411
|
T | G | 53 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0106others(50): Show | 53 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-33600T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625411 | ||||||
| chr4:109625454
|
A | G | 44 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0106others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-33557A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625454 | ||||||
| chr4:109625775
|
G | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-33236G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625775 | ||||||
| chr4:109625872
|
C | A | 3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-33139C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625872 | ||||||
| chr4:109625893
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0280 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-33118C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625893 | ||||||
| chr4:109625899
|
A | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-33112A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625899 | ||||||
| chr4:109625960
|
C | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(256): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.100-33051C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625960 | ||||||
| chr4:109626273
|
GA | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-32731delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626273 | |||||
| chr4:109626288
|
T | A | 1 | a0003c0003t0001g0286 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.100-32723T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626288 | ||||||
| chr4:109626579
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(1): Show | 4 | HG02723.hp1 HG02895.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-32432G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626579 | ||||||
| chr4:109626587
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-32424C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626587 | ||||||
| chr4:109626631
|
G | C | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.100-32380G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626631 | ||||||
| chr4:109626724
|
T | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(240): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-32287T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626724 | ||||||
| chr4:109626728
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-32283A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626728 | ||||||
| chr4:109626735
|
C | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-32276C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626735 | ||||||
| chr4:109626758
|
A | C | 73 | a0001c0001t0001g0256a0001c0001t0003g0069a0002c0002t0002g0090others(70): Show | 75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-32253A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626758 | ||||||
| chr4:109626768
|
ATGCCATT others(1): Show |
A | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(240): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-32234_100-3222 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626768 | |||||
| chr4:109626821
|
C | CA | 15 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0061others(12): Show | 15 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-32166dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | |||||
| chr4:109626821
|
CA | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0105a0001c0001t0001g0229others(7): Show | 10 | HG01109.hp1 HG02523.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-32166delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | |||||
| chr4:109626821
|
CAAA | C | 23 | a0001c0001t0001g0106a0001c0001t0001g0224a0001c0001t0001g0323others(20): Show | 24 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.100-32168_100-3216 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | |||||
| chr4:109626821
|
CAAAA | C | 122 | a0001c0001t0001g0048a0001c0001t0001g0089a0001c0001t0001g0104others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.100-32169_100-3216 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | |||||
| chr4:109626821
|
CAAAAA | C | 23 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(20): Show | 23 | HG00280.hp2 HG00323.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-32170_100-3216 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | |||||
| chr4:109626864
|
C | T | 2 | a0003c0003t0001g0242a0003c0003t0001g0264 | 2 | NA19007.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.100-32147C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626864 | ||||||
| chr4:109626951
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0040others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-32060T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626951 | ||||||
| chr4:109626992
|
T | C | 151 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0089others(148): Show | 153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.100-32019T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626992 | ||||||
| chr4:109627091
|
G | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-31920G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627091 | ||||||
| chr4:109627129
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.100-31882T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627129 | ||||||
| chr4:109627169
|
A | G | 1 | a0002c0002t0002g0212 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.100-31842A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627169 | ||||||
| chr4:109627215
|
C | CT | 22 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-31789dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109627215 | |||||
| chr4:109627238
|
T | C | 22 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-31773T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627238 | ||||||
| chr4:109627432
|
G | A | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-31579G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627432 | ||||||
| chr4:109627437
|
C | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-31574C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627437 | ||||||
| chr4:109627463
|
G | A | 2 | a0001c0001t0005g0195a0001c0001t0005g0196 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.100-31548G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627463 | ||||||
| chr4:109627540
|
G | A | 2 | a0001c0001t0001g0061a0001c0012t0001g0051 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-31471G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627540 | ||||||
| chr4:109627687
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100-31324C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627687 | ||||||
| chr4:109627744
|
C | T | 1 | a0002c0002t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-31267C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627744 | ||||||
| chr4:109627784
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.100-31227G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627784 | ||||||
| chr4:109627917
|
GA | G | 166 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0089others(163): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.100-31080delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109627917 | |||||
| chr4:109627919
|
A | C | 3 | a0001c0005t0006g0046a0001c0005t0006g0169a0001c0005t0006g0326 | 3 | HG00738.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100-31092A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627919 | ||||||
| chr4:109627926
|
A | G | 1 | a0003c0003t0001g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100-31085A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627926 | ||||||
| chr4:109627997
|
TAA | T | 5 | a0001c0001t0001g0225a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-31013_100-3101 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627997 | ||||||
| chr4:109628021
|
A | G | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-30990A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628021 | ||||||
| chr4:109628076
|
C | G | 2 | a0002c0002t0002g0283a0002c0002t0010g0237 | 2 | NA18961.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.100-30935C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628076 | ||||||
| chr4:109628294
|
A | G | 73 | a0001c0001t0001g0256a0001c0001t0003g0069a0002c0002t0002g0090others(70): Show | 75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-30717A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628294 | ||||||
| chr4:109628549
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30462G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628549 | ||||||
| chr4:109628574
|
A | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30437A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628574 | ||||||
| chr4:109628679
|
C | CG | 3 | a0001c0001t0001g0292a0002c0002t0002g0094a0003c0003t0001g0155 | 3 | HG00741.hp1 HG02717.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.100-30330dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109628679 | |||||
| chr4:109628710
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0004g0016others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-30301G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628710 | ||||||
| chr4:109628763
|
C | A | 178 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(175): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.100-30248C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628763 | ||||||
| chr4:109628859
|
C | G | 1 | a0002c0002t0002g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.100-30152C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628859 | ||||||
| chr4:109628903
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0331 | 3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-30108A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628903 | ||||||
| chr4:109628953
|
C | T | 3 | a0001c0001t0004g0055a0003c0003t0001g0053a0003c0003t0001g0054 | 3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-30058C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628953 | ||||||
| chr4:109629040
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.100-29971G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629040 | ||||||
| chr4:109629467
|
C | T | 1 | a0003c0003t0001g0276 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100-29544C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629467 | ||||||
| chr4:109629495
|
A | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-29516A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629495 | ||||||
| chr4:109629565
|
G | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-29446G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629565 | ||||||
| chr4:109629662
|
C | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.100-29349C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629662 | ||||||
| chr4:109629795
|
T | C | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-29216T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629795 | ||||||
| chr4:109629801
|
C | G | 1 | a0003c0003t0001g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.100-29210C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629801 | ||||||
| chr4:109629898
|
C | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(6): Show | 10 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-29113C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629898 | ||||||
| chr4:109629903
|
C | G | 3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-29108C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629903 | ||||||
| chr4:109629966
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.100-29045C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629966 | ||||||
| chr4:109630063
|
C | T | 4 | a0001c0001t0008g0200a0001c0006t0005g0002a0001c0006t0005g0128others(1): Show | 5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-28948C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630063 | ||||||
| chr4:109630152
|
CTTTTT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.100-28858_100-2885 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630152 | ||||||
| chr4:109630196
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.100-28815T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630196 | ||||||
| chr4:109630233
|
G | A | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-28778G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630233 | ||||||
| chr4:109630267
|
A | G | 5 | a0001c0001t0003g0132a0001c0001t0003g0133a0001c0001t0003g0193others(2): Show | 5 | HG02083.hp1 HG02129.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-28744A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630267 | ||||||
| chr4:109630445
|
C | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.100-28566C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630445 | ||||||
| chr4:109630548
|
T | C | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-28463T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630548 | ||||||
| chr4:109630569
|
TTTTG | T | 87 | a0001c0001t0003g0231a0001c0001t0004g0055a0001c0001t0005g0095others(84): Show | 89 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-28426_100-2842 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109630569 | |||||
| chr4:109630625
|
A | G | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-28386A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630625 | ||||||
| chr4:109630727
|
A | G | 30 | a0002c0002t0002g0075a0002c0002t0002g0083a0002c0002t0002g0100others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.100-28284A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630727 | ||||||
| chr4:109630821
|
C | T | 136 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(133): Show | 139 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.100-28190C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630821 | ||||||
| chr4:109630873
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-28138G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630873 | ||||||
| chr4:109631008
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0172a0001c0001t0001g0174others(1): Show | 4 | HG01070.hp1 HG01433.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-28003T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631008 | ||||||
| chr4:109631614
|
G | A | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-27397G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631614 | ||||||
| chr4:109631984
|
A | G | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-27027A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631984 | ||||||
| chr4:109631985
|
C | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-27026C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631985 | ||||||
| chr4:109632322
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.100-26689G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632322 | ||||||
| chr4:109632355
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-26656G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632355 | ||||||
| chr4:109632356
|
AAATCT | A | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-26647_100-2664 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632356 | |||||
| chr4:109632370
|
A | G | 1 | a0001c0001t0003g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.100-26641A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632370 | ||||||
| chr4:109632398
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.100-26613C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632398 | ||||||
| chr4:109632546
|
G | T | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-26465G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632546 | ||||||
| chr4:109632615
|
C | CT | 39 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.100-26378dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | |||||
| chr4:109632615
|
C | CTT | 110 | a0001c0001t0001g0211a0001c0001t0003g0231a0001c0001t0005g0095others(107): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.100-26379_100-2637 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | |||||
| chr4:109632615
|
C | CTTT | 83 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0049others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.100-26380_100-2637 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | |||||
| chr4:109632615
|
C | CTTTT | 23 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(20): Show | 24 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.100-26381_100-2637 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | |||||
| chr4:109632679
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0040others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-26332G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632679 | ||||||
| chr4:109632709
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-26302G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632709 | ||||||
| chr4:109632857
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.100-26154C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632857 | ||||||
| chr4:109632906
|
C | T | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-26105C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632906 | ||||||
| chr4:109633187
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0323 | 2 | NA18940.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.100-25824A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633187 | ||||||
| chr4:109633241
|
G | A | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-25770G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633241 | ||||||
| chr4:109633275
|
A | AT | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-25726dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109633275 | |||||
| chr4:109633278
|
T | A | 55 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0060others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.100-25733T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633278 | ||||||
| chr4:109633298
|
C | T | 1 | a0004c0004t0001g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-25713C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633298 | ||||||
| chr4:109633343
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-25668C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633343 | ||||||
| chr4:109633353
|
C | T | 3 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0002t0002g0074 | 3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100-25658C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633353 | ||||||
| chr4:109633434
|
AT | A | 136 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(133): Show | 139 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.100-25569delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109633434 | |||||
| chr4:109633504
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0236others(1): Show | 5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-25507C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633504 | ||||||
| chr4:109633691
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.100-25320A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633691 | ||||||
| chr4:109633894
|
G | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-25117G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633894 | ||||||
| chr4:109634171
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-24840C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634171 | ||||||
| chr4:109634211
|
G | A | 2 | a0001c0001t0001g0061a0001c0012t0001g0051 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-24800G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634211 | ||||||
| chr4:109634312
|
A | G | 32 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0036others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-24699A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634312 | ||||||
| chr4:109634351
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100-24660G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634351 | ||||||
| chr4:109634485
|
G | GA | 10 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0001t0005g0222others(7): Show | 10 | HG00738.hp2 HG01346.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-24508dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109634485 | |||||
| chr4:109634485
|
GA | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.100-24508delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109634485 | |||||
| chr4:109634485
|
GAA | G | 89 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.100-24509_100-2450 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109634485 | |||||
| chr4:109634522
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.100-24489G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634522 | ||||||
| chr4:109634832
|
C | T | 1 | a0001c0005t0006g0008 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-24179C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634832 | ||||||
| chr4:109634937
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-24074A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634937 | ||||||
| chr4:109634953
|
C | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-24058C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634953 | ||||||
| chr4:109634972
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.100-24039G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634972 | ||||||
| chr4:109634991
|
C | T | 4 | a0001c0001t0008g0200a0001c0006t0005g0002a0001c0006t0005g0128others(1): Show | 5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-24020C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634991 | ||||||
| chr4:109635172
|
T | C | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-23839T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635172 | ||||||
| chr4:109635272
|
T | C | 1 | a0004c0004t0001g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-23739T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635272 | ||||||
| chr4:109635342
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0004g0016others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-23669C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635342 | ||||||
| chr4:109635474
|
G | T | 2 | a0003c0003t0001g0238a0003c0003t0001g0313 | 2 | HG01168.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.100-23537G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635474 | ||||||
| chr4:109635821
|
T | C | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-23190T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635821 | ||||||
| chr4:109635902
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.100-23109C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635902 | ||||||
| chr4:109635904
|
T | TTA | 60 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-23106_100-2310 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109635904 | |||||
| chr4:109635960
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-23051G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635960 | ||||||
| chr4:109636097
|
T | A | 60 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-22914T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636097 | ||||||
| chr4:109636111
|
A | G | 34 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-22900A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636111 | ||||||
| chr4:109636260
|
C | A | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-22751C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636260 | ||||||
| chr4:109636564
|
G | A | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-22447G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636564 | ||||||
| chr4:109636576
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-22435C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636576 | ||||||
| chr4:109636650
|
C | T | 2 | a0001c0001t0001g0061a0001c0012t0001g0051 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-22361C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636650 | ||||||
| chr4:109636664
|
A | G | 330 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(327): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.100-22347A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636664 | ||||||
| chr4:109636766
|
C | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(11): Show | 14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-22245C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636766 | ||||||
| chr4:109636770
|
G | A | 1 | a0002c0002t0002g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-22241G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636770 | ||||||
| chr4:109636797
|
C | T | 60 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-22214C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636797 | ||||||
| chr4:109636897
|
C | T | 1 | a0001c0006t0005g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.100-22114C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636897 | ||||||
| chr4:109637082
|
G | C | 4 | a0003c0003t0001g0025a0003c0003t0001g0027a0003c0003t0001g0155others(1): Show | 4 | HG02717.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21929G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637082 | ||||||
| chr4:109637105
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-21906G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637105 | ||||||
| chr4:109637239
|
A | C | 14 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(11): Show | 14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-21772A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637239 | ||||||
| chr4:109637320
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21691G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637320 | ||||||
| chr4:109637365
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-21646G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637365 | ||||||
| chr4:109637456
|
A | G | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-21555A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637456 | ||||||
| chr4:109637514
|
A | G | 1 | a0002c0002t0002g0152 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.100-21497A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637514 | ||||||
| chr4:109637536
|
G | A | 11 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-21475G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637536 | ||||||
| chr4:109637655
|
A | G | 3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-21356A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637655 | ||||||
| chr4:109637701
|
G | C | 1 | a0003c0007t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.100-21310G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637701 | ||||||
| chr4:109637747
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0189 | 2 | NA18747.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.100-21264G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637747 | ||||||
| chr4:109637867
|
C | T | 4 | a0002c0002t0002g0120a0002c0002t0002g0121a0002c0002t0002g0124others(1): Show | 4 | HG01081.hp2 HG01123.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-21144C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637867 | ||||||
| chr4:109637873
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-21138G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637873 | ||||||
| chr4:109638026
|
T | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20985T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638026 | ||||||
| chr4:109638027
|
GTTTGT | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082 | 3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-20971_100-2096 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638027 | |||||
| chr4:109638174
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-20837G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638174 | ||||||
| chr4:109638285
|
A | C | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0331 | 3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-20726A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638285 | ||||||
| chr4:109638396
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-20615C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638396 | ||||||
| chr4:109638411
|
T | TA | 16 | a0001c0001t0001g0105a0001c0001t0001g0185a0001c0001t0001g0221others(13): Show | 17 | HG00140.hp1 HG00642.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-20582dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | |||||
| chr4:109638411
|
TA | T | 24 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0280others(21): Show | 25 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-20582delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | |||||
| chr4:109638411
|
TAA | T | 22 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(19): Show | 22 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-20583_100-2058 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | |||||
| chr4:109638411
|
TAAA | T | 87 | a0001c0001t0001g0061a0001c0012t0001g0051a0002c0002t0002g0007others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-20584_100-2058 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | |||||
| chr4:109638436
|
A | G | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20575A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638436 | ||||||
| chr4:109638441
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-20570G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638441 | ||||||
| chr4:109638465
|
G | A | 4 | a0003c0003t0001g0025a0003c0003t0001g0027a0003c0003t0001g0155others(1): Show | 4 | HG02717.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20546G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638465 | ||||||
| chr4:109638516
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100-20495G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638516 | ||||||
| chr4:109638573
|
G | A | 1 | a0002c0002t0002g0142 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.100-20438G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638573 | ||||||
| chr4:109638688
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-20323C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638688 | ||||||
| chr4:109639127
|
A | G | 1 | a0001c0012t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.100-19884A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639127 | ||||||
| chr4:109639264
|
G | C | 17 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-19747G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639264 | ||||||
| chr4:109639339
|
T | C | 46 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(43): Show | 46 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-19672T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639339 | ||||||
| chr4:109639350
|
C | CT | 42 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0052others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.100-19649dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109639350 | |||||
| chr4:109639694
|
A | G | 34 | a0001c0001t0001g0061a0001c0001t0003g0003a0001c0001t0003g0011others(31): Show | 35 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-19317A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639694 | ||||||
| chr4:109639752
|
G | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-19259G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639752 | ||||||
| chr4:109639760
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-19251G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639760 | ||||||
| chr4:109639899
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-19112C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639899 | ||||||
| chr4:109639933
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-19078G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639933 | ||||||
| chr4:109639950
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(240): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-19061A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639950 | ||||||
| chr4:109640151
|
A | G | 49 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.100-18860A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640151 | ||||||
| chr4:109640203
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(98): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.100-18808C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640203 | ||||||
| chr4:109640204
|
G | A | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.100-18807G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640204 | ||||||
| chr4:109640379
|
A | G | 2 | a0002c0002t0002g0112a0002c0002t0002g0248 | 2 | HG02523.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.100-18632A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640379 | ||||||
| chr4:109640457
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0009g0108a0004c0004t0001g0331 | 3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-18554C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640457 | ||||||
| chr4:109640784
|
T | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-18227T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640784 | ||||||
| chr4:109641044
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17967T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641044 | ||||||
| chr4:109641087
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.100-17924A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641087 | ||||||
| chr4:109641122
|
TAG | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-17886_100-1788 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641122 | |||||
| chr4:109641178
|
C | T | 16 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(13): Show | 17 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-17833C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641178 | ||||||
| chr4:109641267
|
AT | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.100-17726delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641267 | |||||
| chr4:109641267
|
ATT | A | 24 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(21): Show | 25 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-17727_100-1772 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641267 | |||||
| chr4:109641270
|
T | A | 1 | a0002c0002t0002g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-17741T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641270 | ||||||
| chr4:109641416
|
TATTA | T | 7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-17585_100-1758 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641416 | |||||
| chr4:109641430
|
G | A | 5 | a0003c0003t0001g0234a0003c0003t0001g0235a0003c0003t0001g0261others(2): Show | 5 | HG01257.hp2 HG01517.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-17581G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641430 | ||||||
| chr4:109641550
|
T | A | 1 | a0002c0002t0002g0311 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.100-17461T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641550 | ||||||
| chr4:109641677
|
T | G | 1 | a0002c0002t0002g0090 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.100-17334T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641677 | ||||||
| chr4:109641780
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.100-17231C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641780 | ||||||
| chr4:109641804
|
A | G | 4 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0059others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17207A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641804 | ||||||
| chr4:109641843
|
T | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-17168T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641843 | ||||||
| chr4:109642084
|
C | T | 2 | a0002c0002t0002g0130a0002c0002t0002g0157 | 2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.100-16927C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642084 | ||||||
| chr4:109642143
|
T | A | 2 | a0003c0003t0001g0119a0003c0003t0001g0255 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.100-16868T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642143 | ||||||
| chr4:109642251
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.100-16760A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642251 | ||||||
| chr4:109642294
|
A | G | 17 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-16717A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642294 | ||||||
| chr4:109642311
|
C | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-16700C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642311 | ||||||
| chr4:109642333
|
C | T | 1 | a0003c0003t0001g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100-16678C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642333 | ||||||
| chr4:109642482
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(176): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.100-16529T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642482 | ||||||
| chr4:109642611
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-16400C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642611 | ||||||
| chr4:109642636
|
G | GA | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(240): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.100-16373dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642636 | |||||
| chr4:109642807
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-16204T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642807 | ||||||
| chr4:109642811
|
C | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-16200C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642811 | ||||||
| chr4:109642893
|
A | AT | 16 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0004g0045others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-16098dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | |||||
| chr4:109642893
|
A | ATT | 9 | a0001c0001t0004g0016a0001c0001t0004g0018a0001c0001t0004g0019others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-16099_100-1609 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | |||||
| chr4:109642893
|
AT | A | 83 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136others(80): Show | 84 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.100-16098delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | |||||
| chr4:109642893
|
ATT | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(144): Show | 150 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.100-16099_100-1609 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | |||||
| chr4:109642893
|
ATTT | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0089others(44): Show | 48 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.100-16100_100-1609 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | |||||
| chr4:109642939
|
G | A | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-16072G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642939 | ||||||
| chr4:109642942
|
C | A | 1 | a0002c0011t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100-16069C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642942 | ||||||
| chr4:109642984
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(190): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.100-16027G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642984 | ||||||
| chr4:109643117
|
GA | G | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15891delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109643117 | |||||
| chr4:109643275
|
T | TC | 138 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0048others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100-15734dupC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109643275 | |||||
| chr4:109643374
|
G | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-15637G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643374 | ||||||
| chr4:109643723
|
A | G | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-15288A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643723 | ||||||
| chr4:109643850
|
A | G | 1 | a0001c0001t0004g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-15161A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643850 | ||||||
| chr4:109643891
|
C | G | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15120C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643891 | ||||||
| chr4:109644012
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-14999G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644012 | ||||||
| chr4:109644049
|
A | G | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-14962A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644049 | ||||||
| chr4:109644077
|
G | A | 2 | a0003c0003t0001g0201a0007c0010t0001g0241 | 2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.100-14934G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644077 | ||||||
| chr4:109644272
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.100-14739G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644272 | ||||||
| chr4:109644367
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.100-14644A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644367 | ||||||
| chr4:109644450
|
A | C | 3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-14561A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644450 | ||||||
| chr4:109644505
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.100-14506A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644505 | ||||||
| chr4:109644721
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-14290C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644721 | ||||||
| chr4:109645129
|
T | C | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-13882T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645129 | ||||||
| chr4:109645273
|
T | C | 1 | a0002c0002t0002g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-13738T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645273 | ||||||
| chr4:109645346
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-13665G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645346 | ||||||
| chr4:109645378
|
A | ACCTTAAC others(61): Show |
7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-13618_100-1361 others(72): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109645378 | |||||
| chr4:109645513
|
GA | G | 79 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(76): Show | 81 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.100-13484delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109645513 | |||||
| chr4:109645513
|
GAA | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(95): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.100-13485_100-1348 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109645513 | |||||
| chr4:109645532
|
C | G | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-13479C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645532 | ||||||
| chr4:109645578
|
G | A | 32 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0036others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-13433G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645578 | ||||||
| chr4:109645693
|
A | G | 2 | a0002c0002t0002g0141a0002c0002t0002g0203 | 2 | NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.100-13318A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645693 | ||||||
| chr4:109645702
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0209 | 2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.100-13309C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645702 | ||||||
| chr4:109645811
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-13200C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645811 | ||||||
| chr4:109646000
|
G | A | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-13011G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646000 | ||||||
| chr4:109646025
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-12986C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646025 | ||||||
| chr4:109646060
|
G | C | 1 | a0002c0002t0002g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-12951G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646060 | ||||||
| chr4:109646118
|
C | G | 7 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0058others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-12893C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646118 | ||||||
| chr4:109646256
|
T | G | 34 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-12755T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646256 | ||||||
| chr4:109646303
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-12708G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646303 | ||||||
| chr4:109646317
|
G | A | 155 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(152): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.100-12694G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646317 | ||||||
| chr4:109646341
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0325a0001c0001t0004g0016others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-12670C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646341 | ||||||
| chr4:109646430
|
T | G | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-12581T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646430 | ||||||
| chr4:109646489
|
T | C | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-12522T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646489 | ||||||
| chr4:109646602
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(190): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.100-12409A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646602 | ||||||
| chr4:109646642
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-12369A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646642 | ||||||
| chr4:109646777
|
A | G | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-12234A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646777 | ||||||
| chr4:109646900
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-12111T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646900 | ||||||
| chr4:109646958
|
A | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-12053A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646958 | ||||||
| chr4:109647000
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-12011T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647000 | ||||||
| chr4:109647065
|
C | T | 1 | a0001c0001t0005g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100-11946C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647065 | ||||||
| chr4:109647066
|
G | A | 34 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-11945G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647066 | ||||||
| chr4:109647196
|
C | T | 2 | a0003c0007t0001g0269a0003c0007t0001g0308 | 2 | HG02155.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.100-11815C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647196 | ||||||
| chr4:109647274
|
G | A | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-11737G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647274 | ||||||
| chr4:109647346
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(205): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.100-11665C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647346 | ||||||
| chr4:109647460
|
T | G | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-11551T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647460 | ||||||
| chr4:109647555
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-11456C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647555 | ||||||
| chr4:109647618
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-11393G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647618 | ||||||
| chr4:109647635
|
C | T | 41 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0106others(38): Show | 41 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.100-11376C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647635 | ||||||
| chr4:109647714
|
T | TA | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-11295dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109647714 | |||||
| chr4:109647745
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-11266G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647745 | ||||||
| chr4:109647759
|
A | G | 4 | a0001c0001t0008g0200a0001c0006t0005g0002a0001c0006t0005g0128others(1): Show | 5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-11252A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647759 | ||||||
| chr4:109647795
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-11216C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647795 | ||||||
| chr4:109647795
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-11216C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647795 | ||||||
| chr4:109647796
|
G | A | 8 | a0002c0002t0002g0129a0002c0002t0002g0139a0002c0002t0002g0159others(5): Show | 8 | HG01168.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-11215G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647796 | ||||||
| chr4:109647929
|
C | T | 1 | a0004c0004t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-11082C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647929 | ||||||
| chr4:109647935
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-11076G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647935 | ||||||
| chr4:109648222
|
AAG | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-10779_100-1077 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648222 | |||||
| chr4:109648375
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10636A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648375 | ||||||
| chr4:109648376
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10635G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648376 | ||||||
| chr4:109648379
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10632G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648379 | ||||||
| chr4:109648380
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10631G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648380 | ||||||
| chr4:109648382
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10629G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648382 | ||||||
| chr4:109648385
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10626A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648385 | ||||||
| chr4:109648387
|
T | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10624T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648387 | ||||||
| chr4:109648389
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10622A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648389 | ||||||
| chr4:109648391
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(238): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-10620T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648391 | ||||||
| chr4:109648392
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10619G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648392 | ||||||
| chr4:109648399
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-10612G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648399 | ||||||
| chr4:109648436
|
A | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-10575A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648436 | ||||||
| chr4:109648458
|
C | T | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-10553C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648458 | ||||||
| chr4:109648464
|
C | T | 1 | a0002c0002t0002g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.100-10547C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648464 | ||||||
| chr4:109648574
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10437G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648574 | ||||||
| chr4:109648583
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.100-10428A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648583 | ||||||
| chr4:109648694
|
A | AT | 52 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(49): Show | 53 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.100-10300dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648694 | |||||
| chr4:109648694
|
AT | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-10300delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648694 | |||||
| chr4:109648724
|
CAA | C | 78 | a0001c0001t0001g0066a0001c0001t0004g0055a0001c0006t0005g0002others(75): Show | 81 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.100-10271_100-1027 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648724 | |||||
| chr4:109648724
|
CAAA | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(158): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.100-10272_100-1027 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648724 | |||||
| chr4:109648939
|
G | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-10072G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648939 | ||||||
| chr4:109648953
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(1): Show | 4 | HG02723.hp1 HG02895.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-10058C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648953 | ||||||
| chr4:109648983
|
TTTTA | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-10020_100-1001 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648983 | |||||
| chr4:109649013
|
A | G | 1 | a0004c0004t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-9998A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649013 | ||||||
| chr4:109649024
|
C | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-9987C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649024 | ||||||
| chr4:109649055
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-9956C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649055 | ||||||
| chr4:109649111
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-9900A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649111 | ||||||
| chr4:109649155
|
TC | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-9854delC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109649155 | |||||
| chr4:109649463
|
C | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-9548C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649463 | ||||||
| chr4:109649475
|
G | A | 2 | a0001c0001t0001g0006a0003c0003t0001g0053 | 2 | HG01975.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-9536G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649475 | ||||||
| chr4:109649751
|
T | TAAAATA | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-9259_100-9254d others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109649751 | |||||
| chr4:109649761
|
A | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9250A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649761 | ||||||
| chr4:109649810
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-9201A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649810 | ||||||
| chr4:109649835
|
A | G | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-9176A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649835 | ||||||
| chr4:109649952
|
A | G | 6 | a0004c0004t0001g0013a0004c0004t0001g0033a0004c0004t0001g0034others(3): Show | 6 | HG02622.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-9059A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649952 | ||||||
| chr4:109649986
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0209 | 2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.100-9025G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649986 | ||||||
| chr4:109650025
|
T | C | 49 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(46): Show | 50 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-8986T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650025 | ||||||
| chr4:109650054
|
C | A | 49 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(46): Show | 50 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-8957C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650054 | ||||||
| chr4:109650208
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8803C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650208 | ||||||
| chr4:109650439
|
A | G | 3 | a0002c0002t0002g0007a0002c0002t0002g0199a0002c0002t0002g0206 | 3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.100-8572A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650439 | ||||||
| chr4:109650969
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-8042T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650969 | ||||||
| chr4:109651051
|
C | A | 1 | a0001c0001t0005g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-7960C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651051 | ||||||
| chr4:109651187
|
C | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(95): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.100-7824C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651187 | ||||||
| chr4:109651194
|
C | T | 1 | a0002c0002t0002g0075 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.100-7817C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651194 | ||||||
| chr4:109651877
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-7134T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651877 | ||||||
| chr4:109651945
|
C | T | 6 | a0002c0002t0002g0141a0002c0002t0002g0143a0002c0002t0002g0153others(3): Show | 6 | HG01993.hp2 NA18961.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-7066C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651945 | ||||||
| chr4:109652095
|
C | T | 1 | a0003c0003t0001g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100-6916C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652095 | ||||||
| chr4:109652115
|
A | G | 1 | a0001c0006t0005g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-6896A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652115 | ||||||
| chr4:109652183
|
C | T | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-6828C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652183 | ||||||
| chr4:109652226
|
G | A | 1 | a0003c0003t0007g0005 | 2 | HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.100-6785G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652226 | ||||||
| chr4:109652264
|
G | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-6747G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652264 | ||||||
| chr4:109652294
|
TTC | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-6715_100-6714d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109652294 | |||||
| chr4:109652587
|
C | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-6424C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652587 | ||||||
| chr4:109652595
|
G | C | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-6416G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652595 | ||||||
| chr4:109652693
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-6318T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652693 | ||||||
| chr4:109652716
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-6295T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652716 | ||||||
| chr4:109652746
|
T | G | 1 | a0001c0001t0003g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.100-6265T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652746 | ||||||
| chr4:109652827
|
C | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-6184C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652827 | ||||||
| chr4:109652890
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6121C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652890 | ||||||
| chr4:109652893
|
C | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.100-6118C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652893 | ||||||
| chr4:109653089
|
C | T | 68 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(65): Show | 69 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.100-5922C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653089 | ||||||
| chr4:109653092
|
T | A | 32 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0036others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-5919T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653092 | ||||||
| chr4:109653103
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100-5908G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653103 | ||||||
| chr4:109653114
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.100-5897C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653114 | ||||||
| chr4:109653319
|
C | T | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-5692C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653319 | ||||||
| chr4:109653357
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-5654G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653357 | ||||||
| chr4:109653381
|
G | GA | 39 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0106others(36): Show | 39 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-5617dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109653381 | |||||
| chr4:109653453
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-5558A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653453 | ||||||
| chr4:109653486
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-5525G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653486 | ||||||
| chr4:109653884
|
C | A | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-5127C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653884 | ||||||
| chr4:109653899
|
T | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5112T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653899 | ||||||
| chr4:109653954
|
G | A | 17 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-5057G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653954 | ||||||
| chr4:109654117
|
GT | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-4884delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109654117 | |||||
| chr4:109654241
|
C | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-4770C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654241 | ||||||
| chr4:109654510
|
G | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-4501G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654510 | ||||||
| chr4:109654566
|
G | A | 1 | a0004c0004t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.100-4445G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654566 | ||||||
| chr4:109654694
|
T | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0295 | 3 | HG00642.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.100-4317T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654694 | ||||||
| chr4:109654792
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-4219T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654792 | ||||||
| chr4:109654897
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-4114C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654897 | ||||||
| chr4:109654998
|
A | G | 1 | a0003c0003t0001g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.100-4013A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654998 | ||||||
| chr4:109655082
|
T | G | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-3929T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655082 | ||||||
| chr4:109655327
|
C | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-3684C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655327 | ||||||
| chr4:109655332
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-3679T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655332 | ||||||
| chr4:109655530
|
C | T | 3 | a0001c0001t0004g0055a0003c0003t0001g0053a0003c0003t0001g0054 | 3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-3481C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655530 | ||||||
| chr4:109655547
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-3464G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655547 | ||||||
| chr4:109655550
|
C | T | 1 | a0004c0004t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-3461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655550 | ||||||
| chr4:109655667
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(171): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.100-3344G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655667 | ||||||
| chr4:109655731
|
C | T | 1 | a0004c0004t0001g0331 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-3280C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655731 | ||||||
| chr4:109655741
|
G | A | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-3270G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655741 | ||||||
| chr4:109655773
|
G | A | 1 | a0002c0002t0002g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.100-3238G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655773 | ||||||
| chr4:109655818
|
C | G | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-3193C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655818 | ||||||
| chr4:109656135
|
A | G | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-2876A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656135 | ||||||
| chr4:109656207
|
T | C | 49 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(46): Show | 50 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-2804T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656207 | ||||||
| chr4:109656354
|
C | CT | 30 | a0002c0002t0002g0010a0002c0002t0002g0072a0002c0002t0002g0074others(27): Show | 30 | HG01123.hp1 HG01168.hp1 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.100-2619dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
C | CTT | 29 | a0002c0002t0002g0012a0002c0002t0002g0031a0002c0002t0002g0042others(26): Show | 29 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-2620_100-2619d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
C | CTTTTTTT others(8): Show |
1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.100-2633_100-2619d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0002g0067a0001c0001t0002g0327a0001c0001t0005g0097others(2): Show | 5 | HG00438.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2629_100-2619d others(13): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
CTTTTTTT others(5): Show |
C | 39 | a0001c0001t0001g0300a0001c0001t0002g0038a0001c0001t0002g0044others(36): Show | 39 | HG00423.hp1 HG00621.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-2630_100-2619d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
CTTTTTTT others(6): Show |
C | 77 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(74): Show | 80 | HG00280.hp1 HG00544.hp1 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.100-2631_100-2619d others(15): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
CTTTTTTT others(7): Show |
C | 16 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0001t0004g0019others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-2632_100-2619d others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656354
|
CTTTTTTT others(8): Show |
C | 9 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(6): Show | 9 | HG00738.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2633_100-2619d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | |||||
| chr4:109656378
|
TTTTTTTT others(8): Show |
T | 40 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0071others(37): Show | 40 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.100-2632_100-2618d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656378 | ||||||
| chr4:109656379
|
TTTTTTTT others(7): Show |
T | 53 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0023others(50): Show | 55 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.100-2631_100-2618d others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656379 | ||||||
| chr4:109656380
|
TTTTTTTT others(6): Show |
T | 5 | a0001c0001t0001g0006a0001c0001t0003g0036a0001c0001t0003g0077others(2): Show | 5 | HG01884.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2630_100-2618d others(15): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656380 | ||||||
| chr4:109656381
|
T | G | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-2630T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656381 | ||||||
| chr4:109656387
|
T | G | 14 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(11): Show | 14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-2624T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656387 | ||||||
| chr4:109656463
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-2548T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656463 | ||||||
| chr4:109656558
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-2453T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656558 | ||||||
| chr4:109656580
|
T | C | 1 | a0004c0004t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-2431T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656580 | ||||||
| chr4:109656613
|
C | A | 2 | a0001c0005t0006g0169a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.100-2398C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656613 | ||||||
| chr4:109656652
|
G | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-2359G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656652 | ||||||
| chr4:109656726
|
A | G | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-2285A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656726 | ||||||
| chr4:109656777
|
T | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2234T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656777 | ||||||
| chr4:109656990
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-2021C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656990 | ||||||
| chr4:109657080
|
A | G | 1 | a0003c0003t0001g0281 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-1931A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657080 | ||||||
| chr4:109657218
|
C | CA | 12 | a0001c0001t0001g0032a0001c0001t0001g0068a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG02055.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-1772dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | |||||
| chr4:109657218
|
CA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(97): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.100-1772delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | |||||
| chr4:109657218
|
CAA | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0001g0293others(16): Show | 19 | HG00735.hp1 HG01109.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-1773_100-1772d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | |||||
| chr4:109657218
|
CAAAA | C | 83 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.100-1775_100-1772d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | |||||
| chr4:109657239
|
AT | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0327 | 3 | HG02055.hp2 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.100-1771delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657239 | ||||||
| chr4:109657244
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.100-1767A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657244 | ||||||
| chr4:109657266
|
T | C | 1 | a0002c0002t0002g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100-1745T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657266 | ||||||
| chr4:109657333
|
A | C | 1 | a0002c0002t0002g0248 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-1678A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657333 | ||||||
| chr4:109657410
|
AT | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-1595delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657410 | |||||
| chr4:109657467
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0325a0001c0001t0004g0016others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-1544C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657467 | ||||||
| chr4:109657562
|
G | GCC | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-1449_100-1448i others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657562 | ||||||
| chr4:109657590
|
T | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-1421T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657590 | ||||||
| chr4:109657779
|
A | G | 1 | a0002c0002t0002g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-1232A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657779 | ||||||
| chr4:109657829
|
T | C | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-1182T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657829 | ||||||
| chr4:109657847
|
C | A | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-1164C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657847 | ||||||
| chr4:109657849
|
A | T | 3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-1162A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657849 | ||||||
| chr4:109657893
|
T | C | 1 | a0002c0002t0002g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100-1118T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657893 | ||||||
| chr4:109658033
|
G | A | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.100-978G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658033 | ||||||
| chr4:109658183
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-828G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658183 | ||||||
| chr4:109658229
|
G | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(11): Show | 14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-782G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658229 | ||||||
| chr4:109658237
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-774T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658237 | ||||||
| chr4:109658328
|
G | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-683G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658328 | ||||||
| chr4:109658331
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-680C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658331 | ||||||
| chr4:109658337
|
A | G | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-674A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658337 | ||||||
| chr4:109658379
|
A | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-632A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658379 | ||||||
| chr4:109658422
|
C | T | 1 | a0002c0002t0002g0283 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.100-589C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658422 | ||||||
| chr4:109658630
|
C | T | 135 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.100-381C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658630 | ||||||
| chr4:109658680
|
T | G | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-331T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658680 | ||||||
| chr4:109658761
|
G | A | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.100-250G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658761 | ||||||
| chr4:109658787
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-224C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658787 | ||||||
| chr4:109658928
|
G | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-83G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658928 | ||||||
| chr4:109659154
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.175+68C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659154 | ||||||
| chr4:109659154
|
C | T | 1 | a0003c0003t0001g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175+68C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659154 | ||||||
| chr4:109659280
|
G | GC | 329 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(326): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.175+194_175+195ins others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659280 | ||||||
| chr4:109659313
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+227C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659313 | ||||||
| chr4:109659375
|
A | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+289A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659375 | ||||||
| chr4:109659403
|
A | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+317A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659403 | ||||||
| chr4:109659651
|
A | C | 1 | a0003c0003t0001g0259 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.176-544A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659651 | ||||||
| chr4:109659696
|
A | G | 1 | a0002c0002t0002g0248 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.176-499A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659696 | ||||||
| chr4:109659760
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-435C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659760 | ||||||
| chr4:109659763
|
C | T | 2 | a0001c0001t0004g0227a0001c0001t0004g0297 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.176-432C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659763 | ||||||
| chr4:109659793
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.176-402A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659793 | ||||||
| chr4:109659816
|
C | T | 1 | a0001c0001t0004g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.176-379C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659816 | ||||||
| chr4:109659824
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.176-371A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659824 | ||||||
| chr4:109659829
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-366C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659829 | ||||||
| chr4:109659856
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-339C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659856 | ||||||
| chr4:109659888
|
G | A | 1 | a0003c0003t0001g0255 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.176-307G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659888 | ||||||
| chr4:109659949
|
T | C | 2 | a0001c0001t0001g0061a0001c0012t0001g0051 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.176-246T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659949 | ||||||
| chr4:109660092
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-103G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109660092 | ||||||
| chr4:109660143
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.176-52G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109660143 | ||||||
| chr4:109660168
|
A | AT | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-18dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 109660168 | |||||
| chr4:109660413
|
T | G | 2 | a0001c0001t0003g0077a0001c0001t0003g0209 | 2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.346+48T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660413 | ||||||
| chr4:109660536
|
C | T | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+171C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660536 | ||||||
| chr4:109660583
|
G | A | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.346+218G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660583 | ||||||
| chr4:109660591
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0236others(1): Show | 5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+226C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660591 | ||||||
| chr4:109660717
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+352G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660717 | ||||||
| chr4:109660831
|
A | T | 86 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.346+466A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660831 | ||||||
| chr4:109660832
|
A | T | 1 | a0002c0002t0002g0141 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.346+467A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660832 | ||||||
| chr4:109660849
|
A | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+484A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660849 | ||||||
| chr4:109660944
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.346+579T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660944 | ||||||
| chr4:109661047
|
C | T | 2 | a0001c0005t0006g0169a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.346+682C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661047 | ||||||
| chr4:109661080
|
A | G | 1 | a0001c0001t0005g0171 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.346+715A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661080 | ||||||
| chr4:109661268
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0068 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.346+903A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661268 | ||||||
| chr4:109661269
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.346+904C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661269 | ||||||
| chr4:109661444
|
A | G | 1 | a0002c0002t0002g0083 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.346+1079A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661444 | ||||||
| chr4:109661545
|
A | G | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.346+1180A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661545 | ||||||
| chr4:109661651
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0005t0006g0008others(4): Show | 7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+1286G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661651 | ||||||
| chr4:109661668
|
A | C | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+1303A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661668 | ||||||
| chr4:109661716
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+1351G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661716 | ||||||
| chr4:109661805
|
G | A | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+1440G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661805 | ||||||
| chr4:109661994
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.346+1629C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661994 | ||||||
| chr4:109662009
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(241): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.346+1644A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662009 | ||||||
| chr4:109662010
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+1645G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662010 | ||||||
| chr4:109662129
|
T | C | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+1764T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662129 | ||||||
| chr4:109662168
|
G | A | 1 | a0003c0003t0001g0260 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.346+1803G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662168 | ||||||
| chr4:109662264
|
C | T | 3 | a0001c0001t0004g0055a0003c0003t0001g0053a0003c0003t0001g0054 | 3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.346+1899C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662264 | ||||||
| chr4:109662374
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-1916T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662374 | ||||||
| chr4:109662461
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1829C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662461 | ||||||
| chr4:109662799
|
G | A | 1 | a0001c0001t0005g0095 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.347-1491G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662799 | ||||||
| chr4:109662878
|
C | T | 5 | a0003c0003t0001g0234a0003c0003t0001g0235a0003c0003t0001g0261others(2): Show | 5 | HG01257.hp2 HG01517.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-1412C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662878 | ||||||
| chr4:109662975
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0105 | 3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.347-1315A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662975 | ||||||
| chr4:109663059
|
A | G | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1231A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663059 | ||||||
| chr4:109663126
|
T | C | 1 | a0003c0003t0001g0259 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.347-1164T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663126 | ||||||
| chr4:109663131
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.347-1159A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663131 | ||||||
| chr4:109663146
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1144C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663146 | ||||||
| chr4:109663178
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.347-1112G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663178 | ||||||
| chr4:109663447
|
A | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-843A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663447 | ||||||
| chr4:109663539
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-751C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663539 | ||||||
| chr4:109663540
|
A | G | 21 | a0001c0001t0001g0032a0001c0001t0001g0280a0001c0001t0002g0038others(18): Show | 21 | HG01109.hp2 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-750A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663540 | ||||||
| chr4:109663639
|
A | C | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.347-651A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663639 | ||||||
| chr4:109663687
|
A | T | 1 | a0001c0001t0003g0131 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.347-603A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663687 | ||||||
| chr4:109663700
|
G | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0068 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.347-590G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663700 | ||||||
| chr4:109663835
|
G | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-455G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663835 | ||||||
| chr4:109663879
|
AACCCAGT others(37): Show |
A | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-406_347-363del others(44): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 109663879 | |||||
| chr4:109664152
|
T | C | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-138T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109664152 | ||||||
| chr4:109664422
|
C | CT | 173 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(170): Show | 176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.451+45dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664422 | |||||
| chr4:109664422
|
CT | C | 13 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.451+45delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664422 | |||||
| chr4:109664489
|
G | A | 204 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(201): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.451+95G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664489 | ||||||
| chr4:109664567
|
T | C | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+173T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664567 | ||||||
| chr4:109664631
|
G | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+237G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664631 | ||||||
| chr4:109664655
|
A | G | 1 | a0002c0002t0002g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.451+261A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664655 | ||||||
| chr4:109664745
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.451+351G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664745 | ||||||
| chr4:109664871
|
T | G | 2 | a0004c0004t0001g0033a0004c0004t0001g0065 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.451+477T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664871 | ||||||
| chr4:109664891
|
G | A | 1 | a0003c0003t0001g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.451+497G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664891 | ||||||
| chr4:109664906
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.451+512A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664906 | ||||||
| chr4:109664911
|
A | G | 6 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0213others(3): Show | 6 | NA18940.hp1 NA18954.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+517A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664911 | ||||||
| chr4:109664943
|
TA | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(140): Show | 147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.451+561delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664943 | |||||
| chr4:109664943
|
TAA | T | 99 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.451+560_451+561del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664943 | |||||
| chr4:109665049
|
G | A | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+655G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665049 | ||||||
| chr4:109665123
|
C | T | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+729C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665123 | ||||||
| chr4:109665138
|
G | A | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+744G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665138 | ||||||
| chr4:109665140
|
G | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+746G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665140 | ||||||
| chr4:109665337
|
G | T | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+943G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665337 | ||||||
| chr4:109665366
|
C | G | 41 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0106others(38): Show | 41 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.451+972C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665366 | ||||||
| chr4:109665389
|
G | A | 4 | a0001c0001t0008g0200a0001c0006t0005g0002a0001c0006t0005g0128others(1): Show | 5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+995G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665389 | ||||||
| chr4:109665418
|
A | G | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+1024A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665418 | ||||||
| chr4:109665444
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.451+1050T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665444 | ||||||
| chr4:109665666
|
TTTG | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+1283_451+1285d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109665666 | |||||
| chr4:109665678
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(188): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.451+1284G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665678 | ||||||
| chr4:109665993
|
A | G | 5 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1599A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665993 | ||||||
| chr4:109666265
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451+1871T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666265 | ||||||
| chr4:109666433
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+2039C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666433 | ||||||
| chr4:109666442
|
C | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+2048C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666442 | ||||||
| chr4:109666443
|
A | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+2049A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666443 | ||||||
| chr4:109666552
|
T | TG | 89 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.451+2159dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109666552 | |||||
| chr4:109666582
|
C | A | 1 | a0003c0003t0001g0267 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.451+2188C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666582 | ||||||
| chr4:109666783
|
C | T | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+2389C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666783 | ||||||
| chr4:109666872
|
C | T | 3 | a0002c0002t0002g0092a0002c0002t0002g0094a0002c0002t0002g0096 | 3 | HG02040.hp2 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.451+2478C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666872 | ||||||
| chr4:109666929
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+2535G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666929 | ||||||
| chr4:109666940
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+2546C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666940 | ||||||
| chr4:109667033
|
T | C | 1 | a0004c0004t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.451+2639T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667033 | ||||||
| chr4:109667122
|
C | T | 2 | a0001c0005t0006g0169a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.451+2728C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667122 | ||||||
| chr4:109667147
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+2753G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667147 | ||||||
| chr4:109667199
|
A | C | 1 | a0001c0001t0003g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.451+2805A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667199 | ||||||
| chr4:109667213
|
G | A | 2 | a0001c0005t0006g0169a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.451+2819G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667213 | ||||||
| chr4:109667381
|
A | G | 1 | a0001c0001t0005g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.451+2987A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667381 | ||||||
| chr4:109667428
|
A | C | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+3034A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667428 | ||||||
| chr4:109667575
|
A | G | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+3181A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667575 | ||||||
| chr4:109667714
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+3320C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667714 | ||||||
| chr4:109667801
|
C | T | 116 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.451+3407C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667801 | ||||||
| chr4:109667933
|
A | T | 1 | a0002c0002t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.451+3539A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667933 | ||||||
| chr4:109667962
|
G | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+3568G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667962 | ||||||
| chr4:109668080
|
G | A | 1 | a0003c0007t0001g0269 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.451+3686G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668080 | ||||||
| chr4:109668120
|
G | C | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+3726G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668120 | ||||||
| chr4:109668322
|
TAGG | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+3931_451+3933d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109668322 | |||||
| chr4:109668440
|
A | G | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+4046A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668440 | ||||||
| chr4:109668560
|
A | G | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+4166A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668560 | ||||||
| chr4:109668698
|
G | GT | 8 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(5): Show | 9 | HG02015.hp2 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+4315dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109668698 | |||||
| chr4:109668785
|
CT | C | 6 | a0001c0001t0005g0095a0001c0001t0005g0097a0001c0001t0005g0195others(3): Show | 6 | HG00438.hp1 HG02738.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+4395delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109668785 | |||||
| chr4:109668823
|
T | C | 3 | a0001c0001t0003g0036a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.451+4429T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668823 | ||||||
| chr4:109669098
|
T | A | 2 | a0003c0003t0001g0257a0003c0003t0001g0258 | 2 | NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.451+4704T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669098 | ||||||
| chr4:109669323
|
G | A | 1 | a0003c0003t0001g0084 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.451+4929G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669323 | ||||||
| chr4:109669323
|
G | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.451+4929G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669323 | ||||||
| chr4:109669387
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.451+4993T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669387 | ||||||
| chr4:109669401
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.451+5007C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669401 | ||||||
| chr4:109669641
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.451+5247T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669641 | ||||||
| chr4:109669664
|
T | C | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+5270T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669664 | ||||||
| chr4:109669665
|
G | A | 137 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.451+5271G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669665 | ||||||
| chr4:109669674
|
A | G | 7 | a0002c0002t0002g0075a0002c0002t0002g0083a0002c0002t0002g0100others(4): Show | 7 | HG00423.hp2 HG00621.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+5280A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669674 | ||||||
| chr4:109669698
|
GT | G | 32 | a0001c0001t0001g0325a0001c0001t0003g0231a0001c0001t0005g0095others(29): Show | 33 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.451+5316delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109669698 | |||||
| chr4:109670118
|
G | A | 101 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.451+5724G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670118 | ||||||
| chr4:109670191
|
A | G | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+5797A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670191 | ||||||
| chr4:109670203
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.451+5809A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670203 | ||||||
| chr4:109670309
|
TACAGGTT others(4): Show |
T | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5917_451+5927d others(13): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109670309 | |||||
| chr4:109670323
|
G | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5929G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670323 | ||||||
| chr4:109670325
|
T | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5931T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670325 | ||||||
| chr4:109670326
|
GGGTTTTT others(3): Show |
G | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5933_451+5942d others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670326 | ||||||
| chr4:109670337
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5943T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670337 | ||||||
| chr4:109670584
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+6190C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670584 | ||||||
| chr4:109670621
|
C | T | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+6227C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670621 | ||||||
| chr4:109670630
|
C | T | 1 | a0001c0001t0005g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.451+6236C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670630 | ||||||
| chr4:109670647
|
C | T | 1 | a0003c0003t0001g0275 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.451+6253C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670647 | ||||||
| chr4:109670685
|
C | T | 2 | a0001c0001t0001g0061a0001c0012t0001g0051 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.451+6291C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670685 | ||||||
| chr4:109670719
|
C | CA | 28 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(25): Show | 28 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.451+6337dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109670719 | |||||
| chr4:109670879
|
C | T | 1 | a0003c0003t0001g0255 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.451+6485C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670879 | ||||||
| chr4:109670928
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+6534C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670928 | ||||||
| chr4:109670934
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(113): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.451+6540G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670934 | ||||||
| chr4:109670978
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451+6584G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670978 | ||||||
| chr4:109671141
|
T | G | 1 | a0003c0003t0001g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.451+6747T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109671141 | ||||||
| chr4:109671220
|
A | G | 5 | a0001c0005t0006g0008a0001c0005t0006g0009a0001c0005t0006g0046others(2): Show | 5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+6826A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109671220 | ||||||
| chr4:109671306
|
G | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.451+6912G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109671306 | ||||||
| chr4:109671568
|
TC | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+7176delC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109671568 | |||||
| chr4:109672304
|
A | C | 101 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.451+7910A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672304 | ||||||
| chr4:109672444
|
A | T | 108 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0060others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.451+8050A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672444 | ||||||
| chr4:109672531
|
A | G | 1 | a0002c0002t0002g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.451+8137A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672531 | ||||||
| chr4:109672692
|
G | A | 1 | a0002c0002t0002g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.451+8298G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672692 | ||||||
| chr4:109672827
|
T | C | 1 | a0003c0003t0001g0164 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.451+8433T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672827 | ||||||
| chr4:109672853
|
C | T | 1 | a0002c0002t0002g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.451+8459C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672853 | ||||||
| chr4:109672898
|
C | G | 1 | a0002c0002t0002g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.451+8504C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672898 | ||||||
| chr4:109673072
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.451+8678T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673072 | ||||||
| chr4:109673232
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.451+8838G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673232 | ||||||
| chr4:109673279
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.451+8885C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673279 | ||||||
| chr4:109673365
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451+8971G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673365 | ||||||
| chr4:109673376
|
C | A | 1 | a0001c0001t0003g0003 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.451+8982C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673376 | ||||||
| chr4:109673475
|
G | A | 1 | a0002c0002t0002g0012 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.451+9081G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673475 | ||||||
| chr4:109673576
|
A | G | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-9006A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673576 | ||||||
| chr4:109673793
|
TGGC | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0105 | 3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.452-8786_452-8784d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109673793 | |||||
| chr4:109673906
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-8676C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673906 | ||||||
| chr4:109674041
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-8541G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674041 | ||||||
| chr4:109674130
|
G | A | 6 | a0004c0004t0001g0013a0004c0004t0001g0033a0004c0004t0001g0034others(3): Show | 6 | HG02622.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-8452G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674130 | ||||||
| chr4:109674150
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-8432G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674150 | ||||||
| chr4:109674251
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.452-8331T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674251 | ||||||
| chr4:109674334
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-8248A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674334 | ||||||
| chr4:109674502
|
T | C | 1 | a0002c0002t0002g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.452-8080T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674502 | ||||||
| chr4:109674533
|
G | A | 1 | a0001c0001t0003g0317 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.452-8049G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674533 | ||||||
| chr4:109674542
|
A | T | 3 | a0003c0003t0001g0314a0003c0003t0001g0315a0003c0003t0001g0316 | 3 | HG02698.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.452-8040A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674542 | ||||||
| chr4:109674677
|
G | A | 4 | a0002c0002t0002g0120a0002c0002t0002g0121a0002c0002t0002g0124others(1): Show | 4 | HG01081.hp2 HG01123.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-7905G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674677 | ||||||
| chr4:109674873
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0280 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-7709T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674873 | ||||||
| chr4:109675056
|
T | C | 1 | a0001c0001t0002g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-7526T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675056 | ||||||
| chr4:109675101
|
AAAAG | A | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-7477_452-7474d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109675101 | |||||
| chr4:109675124
|
C | A | 76 | a0001c0001t0004g0055a0003c0003t0001g0004a0003c0003t0001g0025others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.452-7458C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675124 | ||||||
| chr4:109675703
|
G | T | 3 | a0001c0001t0004g0055a0003c0003t0001g0053a0003c0003t0001g0054 | 3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.452-6879G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675703 | ||||||
| chr4:109675760
|
T | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0003g0003others(32): Show | 36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.452-6822T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675760 | ||||||
| chr4:109675761
|
C | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0003g0003others(32): Show | 36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.452-6821C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675761 | ||||||
| chr4:109675873
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.452-6709G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675873 | ||||||
| chr4:109676226
|
G | A | 1 | a0001c0001t0005g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.452-6356G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109676226 | ||||||
| chr4:109676856
|
A | G | 1 | a0001c0001t0004g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.452-5726A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109676856 | ||||||
| chr4:109677184
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-5398C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677184 | ||||||
| chr4:109677374
|
A | C | 5 | a0001c0005t0006g0008a0001c0005t0006g0009a0001c0005t0006g0046others(2): Show | 5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-5208A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677374 | ||||||
| chr4:109677467
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0002g0038a0001c0001t0002g0044others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-5115C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677467 | ||||||
| chr4:109677653
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4929C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677653 | ||||||
| chr4:109677674
|
C | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-4908C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677674 | ||||||
| chr4:109677687
|
G | A | 1 | a0002c0002t0002g0080 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.452-4895G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677687 | ||||||
| chr4:109677766
|
T | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4816T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677766 | ||||||
| chr4:109677802
|
A | AT | 57 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(54): Show | 57 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.452-4753dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677802
|
A | ATT | 50 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(47): Show | 52 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.452-4754_452-4753d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677802
|
A | ATTT | 16 | a0001c0001t0003g0133a0001c0001t0005g0097a0001c0001t0005g0171others(13): Show | 17 | HG02071.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-4755_452-4753d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677802
|
A | ATTTT | 7 | a0001c0001t0003g0088a0004c0004t0001g0028a0004c0004t0001g0034others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-4756_452-4753d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677802
|
AT | A | 88 | a0001c0001t0001g0225a0001c0001t0004g0045a0001c0001t0004g0055others(85): Show | 88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.452-4753delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677802
|
ATT | A | 13 | a0001c0001t0001g0068a0001c0001t0001g0280a0001c0001t0001g0299others(10): Show | 13 | HG00140.hp2 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.452-4754_452-4753d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677802
|
ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4764_452-4753d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | |||||
| chr4:109677866
|
G | A | 1 | a0002c0002t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.452-4716G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677866 | ||||||
| chr4:109677918
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.452-4664A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677918 | ||||||
| chr4:109677921
|
C | T | 1 | a0003c0003t0001g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.452-4661C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677921 | ||||||
| chr4:109677980
|
G | C | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4602G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677980 | ||||||
| chr4:109678024
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.452-4558C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678024 | ||||||
| chr4:109678123
|
C | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4459C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678123 | ||||||
| chr4:109678194
|
T | C | 1 | a0002c0002t0002g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.452-4388T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678194 | ||||||
| chr4:109678221
|
G | A | 137 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.452-4361G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678221 | ||||||
| chr4:109678292
|
G | T | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4290G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678292 | ||||||
| chr4:109678317
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.452-4265G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678317 | ||||||
| chr4:109678417
|
G | A | 32 | a0001c0001t0001g0325a0001c0001t0003g0231a0001c0001t0005g0095others(29): Show | 33 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.452-4165G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678417 | ||||||
| chr4:109678455
|
C | T | 4 | a0001c0001t0003g0088a0002c0002t0002g0072a0002c0002t0002g0073others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-4127C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678455 | ||||||
| chr4:109678479
|
G | A | 2 | a0001c0005t0006g0008a0001c0005t0006g0009 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.452-4103G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678479 | ||||||
| chr4:109678500
|
A | G | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-4082A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678500 | ||||||
| chr4:109678513
|
G | T | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-4069G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678513 | ||||||
| chr4:109678532
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4050C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678532 | ||||||
| chr4:109678627
|
C | CG | 9 | a0001c0001t0001g0041a0001c0001t0004g0024a0001c0005t0006g0169others(6): Show | 9 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-3951dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678627 | |||||
| chr4:109678639
|
C | T | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-3943C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678639 | ||||||
| chr4:109678648
|
G | A | 2 | a0004c0004t0001g0033a0004c0004t0001g0065 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.452-3934G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678648 | ||||||
| chr4:109678704
|
CGG | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-3875_452-3874d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678704 | |||||
| chr4:109678744
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.452-3838C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678744 | ||||||
| chr4:109678745
|
G | A | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-3837G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678745 | ||||||
| chr4:109678754
|
G | A | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-3828G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678754 | ||||||
| chr4:109678803
|
G | A | 5 | a0001c0005t0006g0008a0001c0005t0006g0009a0001c0005t0006g0046others(2): Show | 5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-3779G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678803 | ||||||
| chr4:109678806
|
C | T | 2 | a0003c0003t0001g0025a0003c0003t0001g0027 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.452-3776C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678806 | ||||||
| chr4:109678818
|
G | A | 1 | a0002c0002t0002g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.452-3764G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678818 | ||||||
| chr4:109678868
|
C | T | 87 | a0002c0002t0002g0007a0002c0002t0002g0010a0002c0002t0002g0012others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.452-3714C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678868 | ||||||
| chr4:109678869
|
G | A | 2 | a0001c0001t0001g0325a0005c0009t0001g0226 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.452-3713G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678869 | ||||||
| chr4:109678896
|
C | CG | 7 | a0001c0001t0001g0041a0001c0001t0003g0165a0001c0001t0003g0232others(4): Show | 7 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-3682dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678896 | |||||
| chr4:109678904
|
CGGCCGGG others(30): Show |
C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3654_452-3618d others(39): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678904 | |||||
| chr4:109678947
|
G | A | 2 | a0003c0003t0001g0242a0003c0003t0001g0264 | 2 | NA19007.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.452-3635G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678947 | ||||||
| chr4:109678947
|
G | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-3635G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678947 | ||||||
| chr4:109678999
|
C | G | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3583C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678999 | ||||||
| chr4:109679078
|
C | T | 1 | a0003c0003t0001g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.452-3504C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679078 | ||||||
| chr4:109679136
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3446C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679136 | ||||||
| chr4:109679146
|
T | C | 137 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.452-3436T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679146 | ||||||
| chr4:109679184
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0017others(207): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.452-3398A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679184 | ||||||
| chr4:109679240
|
C | CG | 4 | a0001c0001t0004g0024a0001c0001t0005g0095a0001c0001t0005g0195others(1): Show | 4 | HG01243.hp2 HG03098.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-3338dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109679240 | |||||
| chr4:109679240
|
C | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-3342C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679240 | ||||||
| chr4:109679241
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.452-3341G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679241 | ||||||
| chr4:109679249
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.452-3333G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679249 | ||||||
| chr4:109679324
|
C | T | 1 | a0007c0010t0001g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.452-3258C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679324 | ||||||
| chr4:109679325
|
G | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-3257G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679325 | ||||||
| chr4:109679376
|
G | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-3206G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679376 | ||||||
| chr4:109679406
|
G | A | 17 | a0001c0001t0001g0325a0004c0004t0001g0013a0004c0004t0001g0028others(14): Show | 17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-3176G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679406 | ||||||
| chr4:109679412
|
G | A | 116 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.452-3170G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679412 | ||||||
| chr4:109679420
|
C | A | 1 | a0001c0001t0004g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.452-3162C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679420 | ||||||
| chr4:109679433
|
G | A | 1 | a0002c0002t0002g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.452-3149G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679433 | ||||||
| chr4:109679454
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3128C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679454 | ||||||
| chr4:109679460
|
A | G | 1 | a0002c0011t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.452-3122A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679460 | ||||||
| chr4:109679516
|
C | T | 17 | a0001c0001t0001g0017a0001c0001t0004g0016a0001c0001t0004g0018others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.452-3066C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679516 | ||||||
| chr4:109679565
|
C | T | 1 | a0002c0002t0002g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.452-3017C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679565 | ||||||
| chr4:109679598
|
G | A | 15 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(12): Show | 15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-2984G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679598 | ||||||
| chr4:109679604
|
A | G | 1 | a0001c0005t0006g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.452-2978A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679604 | ||||||
| chr4:109679690
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.452-2892G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679690 | ||||||
| chr4:109679772
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(224): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.452-2810G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679772 | ||||||
| chr4:109679787
|
T | TTTGTTGT others(2): Show |
9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-2774_452-2766d others(11): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109679787 | |||||
| chr4:109679787
|
TTTGTTGT others(8): Show |
T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2780_452-2766d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109679787 | |||||
| chr4:109679836
|
G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.452-2746G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679836 | ||||||
| chr4:109679840
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.452-2742C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679840 | ||||||
| chr4:109679841
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(225): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.452-2741A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679841 | ||||||
| chr4:109679858
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2724G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679858 | ||||||
| chr4:109680095
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.452-2487C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680095 | ||||||
| chr4:109680131
|
C | G | 1 | a0002c0002t0002g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.452-2451C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680131 | ||||||
| chr4:109680198
|
T | C | 1 | a0001c0005t0006g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.452-2384T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680198 | ||||||
| chr4:109680322
|
C | G | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-2260C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680322 | ||||||
| chr4:109680518
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0225others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-2064A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680518 | ||||||
| chr4:109680536
|
T | TATGTATA others(314): Show |
1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.452-2033_452-2032i others(323): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | |||||
| chr4:109680536
|
T | TATGTATA others(315): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0280 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-2033_452-2032i others(324): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | |||||
| chr4:109680536
|
T | TATGTATA others(316): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0225a0001c0001t0001g0299others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-2033_452-2032i others(325): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | |||||
| chr4:109680536
|
T | TATGTATA others(317): Show |
3 | a0001c0001t0001g0301a0001c0001t0001g0309a0001c0005t0006g0169 | 3 | HG02559.hp2 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.452-2033_452-2032i others(326): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | |||||
| chr4:109680536
|
T | TATGTATA others(318): Show |
4 | a0001c0005t0006g0008a0001c0005t0006g0009a0001c0005t0006g0046others(1): Show | 4 | HG00738.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-2033_452-2032i others(327): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | |||||
| chr4:109680632
|
A | G | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-1950A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680632 | ||||||
| chr4:109680769
|
C | G | 1 | a0002c0002t0002g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.452-1813C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680769 | ||||||
| chr4:109680880
|
A | G | 32 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0036others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.452-1702A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680880 | ||||||
| chr4:109680973
|
A | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0280 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-1609A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680973 | ||||||
| chr4:109680986
|
A | G | 2 | a0001c0001t0004g0227a0001c0001t0004g0297 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.452-1596A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680986 | ||||||
| chr4:109681274
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.452-1308T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681274 | ||||||
| chr4:109681328
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.452-1254G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681328 | ||||||
| chr4:109681352
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.452-1230T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681352 | ||||||
| chr4:109681446
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-1136G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681446 | ||||||
| chr4:109681480
|
G | A | 3 | a0003c0007t0001g0102a0003c0007t0001g0269a0003c0007t0001g0308 | 3 | HG02155.hp2 NA18949.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.452-1102G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681480 | ||||||
| chr4:109681528
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-1054G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681528 | ||||||
| chr4:109681543
|
G | A | 2 | a0002c0002t0002g0130a0002c0002t0002g0157 | 2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.452-1039G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681543 | ||||||
| chr4:109681587
|
A | G | 1 | a0002c0002t0002g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.452-995A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681587 | ||||||
| chr4:109681597
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-985G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681597 | ||||||
| chr4:109681672
|
G | T | 1 | a0001c0001t0009g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.452-910G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681672 | ||||||
| chr4:109681795
|
A | T | 15 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-787A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681795 | ||||||
| chr4:109681922
|
G | A | 1 | a0002c0002t0002g0199 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.452-660G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681922 | ||||||
| chr4:109681959
|
T | C | 3 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0167 | 3 | HG00323.hp1 HG00642.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.452-623T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681959 | ||||||
| chr4:109682075
|
CTGGT | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.452-503_452-500del others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109682075 | |||||
| chr4:109682090
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.452-492C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682090 | ||||||
| chr4:109682122
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(6): Show | 9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.452-460G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682122 | ||||||
| chr4:109682123
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-459C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682123 | ||||||
| chr4:109682180
|
T | C | 5 | a0001c0005t0006g0008a0001c0005t0006g0009a0001c0005t0006g0046others(2): Show | 5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-402T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682180 | ||||||
| chr4:109682261
|
C | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-321C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682261 | ||||||
| chr4:109682274
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.452-308A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682274 | ||||||
| chr4:109682324
|
C | CT | 191 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(188): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.452-245dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109682324 | |||||
| chr4:109682324
|
CT | C | 24 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0068others(21): Show | 24 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-245delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109682324 | |||||
| chr4:109682335
|
T | G | 1 | a0002c0002t0002g0278 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.452-247T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682335 | ||||||
| chr4:109682838
|
C | G | 1 | a0004c0004t0001g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.612+96C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109682838 | ||||||
| chr4:109682896
|
C | T | 1 | a0004c0004t0001g0034 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.612+154C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109682896 | ||||||
| chr4:109683015
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(5): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.612+273C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683015 | ||||||
| chr4:109683301
|
G | A | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+559G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683301 | ||||||
| chr4:109683429
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.612+687C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683429 | ||||||
| chr4:109683508
|
C | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0052others(25): Show | 28 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.612+766C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683508 | ||||||
| chr4:109683738
|
G | A | 2 | a0003c0003t0001g0053a0003c0003t0001g0054 | 2 | HG01975.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.613-705G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683738 | ||||||
| chr4:109683777
|
G | T | 11 | a0001c0001t0003g0231a0001c0001t0005g0095a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.613-666G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683777 | ||||||
| chr4:109683827
|
C | G | 1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613-616C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683827 | ||||||
| chr4:109683830
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.613-613A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683830 | ||||||
| chr4:109683932
|
T | C | 1 | a0002c0002t0002g0153 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.613-511T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683932 | ||||||
| chr4:109683940
|
T | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(230): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.613-503T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683940 | ||||||
| chr4:109684020
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.613-423C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684020 | ||||||
| chr4:109684058
|
CTCTTT | C | 3 | a0001c0005t0006g0046a0001c0005t0006g0169a0001c0005t0006g0326 | 3 | HG00738.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.613-378_613-374del others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 109684058 | |||||
| chr4:109684065
|
C | CT | 76 | a0001c0001t0001g0173a0001c0001t0003g0003a0001c0001t0003g0011others(73): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.613-363dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 109684065 | |||||
| chr4:109684109
|
CTGGAGTG others(3): Show |
C | 6 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-326_613-317del others(10): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 109684109 | |||||
| chr4:109684278
|
G | C | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0309 | 3 | HG02559.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.613-165G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684278 | ||||||
| chr4:109684284
|
G | A | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684284 | ||||||
| chr4:109684297
|
C | T | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-146C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684297 | ||||||
| chr4:109684298
|
G | A | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-145G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684298 | ||||||
| chr4:109684305
|
G | A | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-138G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684305 | ||||||
| chr4:109684309
|
A | G | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-134A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684309 | ||||||
| chr4:109684314
|
G | A | 3 | a0003c0003t0001g0004a0003c0003t0001g0288a0003c0003t0001g0306 | 4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-129G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684314 | ||||||
| chr4:109684365
|
G | A | 1 | a0001c0001t0003g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.613-78G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684365 | ||||||
| chr4:109684910
|
T | TA | 42 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0082others(39): Show | 42 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.816+272dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 109684910 | |||||
| chr4:109684944
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0325a0005c0009t0001g0226 | 3 | HG02257.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+298G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109684944 | ||||||
| chr4:109684987
|
C | T | 3 | a0003c0003t0001g0314a0003c0003t0001g0315a0003c0003t0001g0316 | 3 | HG02698.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.817-264C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109684987 | ||||||
| chr4:109685064
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.817-187G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109685064 | ||||||
| chr4:109685109
|
T | C | 1 | a0002c0002t0002g0141 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.817-142T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109685109 | ||||||
| chr4:109685235
|
TCTC | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0325a0004c0004t0001g0013others(16): Show | 19 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.817-15_817-13delCT others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109685235 | ||||||
| chr4:109685238
|
C | CT | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(226): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
splice_region_variant&intron_variant | LOW | c.817-4dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 109685238 | |||||
| chr4:109685557
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(188): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.933+190T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109685557 | ||||||
| chr4:109685570
|
A | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+203A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109685570 | ||||||
| chr4:109685661
|
G | A | 3 | a0001c0006t0005g0002a0001c0006t0005g0128a0001c0006t0005g0136 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+294G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109685661 | ||||||
| chr4:109686182
|
C | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.933+815C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686182 | ||||||
| chr4:109686221
|
T | C | 1 | a0002c0002t0002g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.933+854T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686221 | ||||||
| chr4:109686224
|
G | A | 1 | a0003c0003t0001g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.933+857G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686224 | ||||||
| chr4:109686302
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.933+935T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686302 | ||||||
| chr4:109686355
|
T | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0044a0001c0001t0002g0067others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+988T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686355 | ||||||
| chr4:109686398
|
C | G | 2 | a0001c0005t0006g0169a0001c0005t0006g0326 | 2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.933+1031C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686398 | ||||||
| chr4:109686484
|
G | A | 1 | a0003c0003t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.934-1031G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686484 | ||||||
| chr4:109686627
|
G | A | 1 | a0004c0004t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.934-888G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686627 | ||||||
| chr4:109686964
|
GTTTT | G | 16 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-544_934-541del others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 109686964 | |||||
| chr4:109686965
|
T | G | 2 | a0002c0002t0002g0130a0002c0002t0002g0157 | 2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.934-550T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686965 | ||||||
| chr4:109687013
|
CTG | C | 16 | a0004c0004t0001g0013a0004c0004t0001g0028a0004c0004t0001g0030others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-500_934-499del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 109687013 | |||||
| chr4:109687032
|
A | G | 1 | a0002c0002t0002g0075 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.934-483A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687032 | ||||||
| chr4:109687105
|
G | A | 77 | a0003c0003t0001g0004a0003c0003t0001g0025a0003c0003t0001g0027others(74): Show | 79 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.934-410G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687105 | ||||||
| chr4:109687174
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(5): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-341G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687174 | ||||||
| chr4:109687337
|
T | C | 1 | a0004c0004t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.934-178T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687337 | ||||||
| chr4:109687367
|
T | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(5): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-148T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687367 | ||||||
| chr4:109687380
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(234): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.934-135C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687380 |