Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 92597 |
|---|---|
| ensemblid | ENSG00000173542.9 |
| hgncid | 29801 |
| symbol | MOB1B |
| name | MOB kinase activator 1B |
| refseq_nuc | NM_173468.4 |
| refseq_prot | NP_775739.1 |
| ensembl_nuc | ENST00000309395.7 |
| ensembl_prot | ENSP00000310189.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 70902369 |
| end | 70988168 |
| strand | + |
| ver | v1.2 |
| region | chr4:70902369-70988168 |
| region5000 | chr4:70897369-70993168 |
| regionname0 | MOB1B_chr4_70902369_70988168 |
| regionname5000 | MOB1B_chr4_70897369_70993168 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 651 | 282 | 86 | 45 | 111 | 8 | 30 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| c0002 | 0/0 | 651 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| c0003 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 6280 | 141 | 33 | 36 | 52 | 5 | 14 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0002 | 0/0 | 6280 | 41 | 3 | 2 | 34 | 0 | 2 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0003 | 1/0 | 6280 | 21 | 6 | 1 | 9 | 0 | 4 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0004 | 0/0 | 6280 | 15 | 11 | 1 | 0 | 3 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0005 | 0/0 | 6280 | 13 | 1 | 2 | 5 | 0 | 5 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0006 | 0/0 | 6280 | 12 | 10 | 1 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0007 | 0/0 | 6279 | 7 | 7 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0008 | 0/0 | 6280 | 7 | 6 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0009 | 0/0 | 6280 | 5 | 0 | 0 | 5 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0010 | 0/0 | 6280 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0011 | 0/0 | 6280 | 2 | 2 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0012 | 0/0 | 6280 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0013 | 0/0 | 6280 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0014 | 0/0 | 6280 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0015 | 0/0 | 6279 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0016 | 0/0 | 6280 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0017 | 0/0 | 6280 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0018 | 0/0 | 6280 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0019 | 0/0 | 6280 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0020 | 0/0 | 6280 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0021 | 0/0 | 6280 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0022 | 0/0 | 6280 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0023 | 0/0 | 6280 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0024 | 0/0 | 6280 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0025 | 0/0 | 6280 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0026 | 0/0 | 6280 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| t0027 | 0/0 | 6280 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 651 | 282 | 86 | 45 | 111 | 8 | 30 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0002 | 0/0 | 651 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0002c0003 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6930 | 140 | 33 | 36 | 51 | 5 | 14 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0002 | 0/0 | 6930 | 41 | 3 | 2 | 34 | 0 | 2 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0003 | 1/0 | 6930 | 21 | 6 | 1 | 9 | 0 | 4 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0004 | 0/0 | 6930 | 15 | 11 | 1 | 0 | 3 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0005 | 0/0 | 6930 | 13 | 1 | 2 | 5 | 0 | 5 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0006 | 0/0 | 6930 | 11 | 10 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0007 | 0/0 | 6929 | 7 | 7 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0008 | 0/0 | 6930 | 7 | 6 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0009 | 0/0 | 6930 | 5 | 0 | 0 | 5 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0010 | 0/0 | 6930 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0011 | 0/0 | 6930 | 2 | 2 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0012 | 0/0 | 6930 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0013 | 0/0 | 6930 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0014 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0015 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0016 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0017 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0018 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0019 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0020 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0021 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0022 | 0/0 | 6930 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0023 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0024 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0025 | 0/0 | 6930 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0026 | 0/0 | 6930 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0001t0027 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0001c0002t0006 | 0/0 | 6930 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| a0002c0003t0001 | 0/0 | 6930 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | copy fasta | chr4 | 70897369 | 70993168 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0014g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0016g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0018g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0019g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0020g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0021g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0022g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0024g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0025g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0026g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0027g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0002t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0220 | EUR | FIN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0208 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0224 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0052 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01243 | hp2 | a0001 | c0001 | t0026 | g0011 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01261 | hp1 | a0001 | c0001 | t0022 | g0200 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0080 | EUR | IBS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0081 | EUR | IBS | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01884 | hp1 | a0001 | c0001 | t0027 | g0065 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0003 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02132 | hp1 | a0001 | c0001 | t0012 | g0174 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0281 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0083 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0223 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02602 | hp1 | a0001 | c0001 | t0024 | g0063 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0102 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0263 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0002 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02723 | hp2 | a0001 | c0001 | t0017 | g0097 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02738 | hp2 | a0001 | c0001 | t0019 | g0283 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0266 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0275 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0204 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0280 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0078 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0207 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0064 | SAS | STU | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03834 | hp2 | a0001 | c0001 | t0014 | g0203 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0202 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18906 | hp1 | a0001 | c0001 | t0020 | g0261 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18956 | hp2 | a0001 | c0001 | t0013 | g0122 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18968 | hp2 | a0001 | c0001 | t0010 | g0006 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18978 | hp1 | a0001 | c0001 | t0009 | g0181 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18979 | hp2 | a0001 | c0001 | t0025 | g0012 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18983 | hp1 | a0001 | c0001 | t0012 | g0175 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0276 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0070 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19057 | hp1 | a0001 | c0001 | t0013 | g0211 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0252 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19082 | hp2 | a0002 | c0003 | t0001 | g0180 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19083 | hp2 | a0001 | c0001 | t0009 | g0257 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0265 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0262 | AFR | ASW | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20905 | hp2 | a0001 | c0001 | t0021 | g0161 | SAS | GIH | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0279 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | USA | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | USA | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | USA | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0218 | REF | REF | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0072 | REF | REF | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70979138
|
C | A | 1 | a0002 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.420C>A | p.Phe140Leu | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/6 | 588/6930 | 420/651 | 140/216 | chr4 | 70979138 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70979135
|
G | A | 1 | a0001c0002 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.417G>A | p.Pro139Pro | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/6 | 585/6930 | 417/651 | 139/216 | chr4 | 70979135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70902405
|
G | C | 1 | a0001c0001t0010 | 2 | NA18968.hp2 NA19057.hp2 |
5_prime_UTR_variant | MODIFIER | c.-132G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/6 | 132 | chr4 | 70902405 | |||||
| chr4:70902449
|
T | C | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-88T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/6 | 88 | chr4 | 70902449 | |||||
| chr4:70902509
|
C | T | 1 | a0001c0001t0013 | 2 | NA18956.hp2 NA19057.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-28C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/6 | chr4 | 70902509 | ||||||
| chr4:70982143
|
A | T | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0010others(5): Show | 59 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*86A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 86 | chr4 | 70982143 | |||||
| chr4:70982367
|
G | A | 1 | a0001c0001t0014 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*310G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 310 | chr4 | 70982367 | |||||
| chr4:70982428
|
T | C | 3 | a0001c0001t0006a0001c0001t0024a0001c0002t0006 | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*371T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 371 | chr4 | 70982428 | |||||
| chr4:70982969
|
T | C | 1 | a0001c0001t0011 | 2 | HG02886.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*912T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 912 | chr4 | 70982969 | |||||
| chr4:70983030
|
T | C | 1 | a0001c0001t0009 | 5 | HG00408.hp1 NA18978.hp1 NA19003.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*973T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 973 | chr4 | 70983030 | |||||
| chr4:70983076
|
A | G | 1 | a0001c0001t0023 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 1019 | chr4 | 70983076 | |||||
| chr4:70983717
|
T | G | 1 | a0001c0001t0015 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1660T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 1660 | chr4 | 70983717 | |||||
| chr4:70983797
|
C | T | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 1740 | chr4 | 70983797 | |||||
| chr4:70983980
|
C | T | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(21): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*1923C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 1923 | chr4 | 70983980 | |||||
| chr4:70984171
|
G | T | 11 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(8): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*2114G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 2114 | chr4 | 70984171 | |||||
| chr4:70984554
|
A | G | 3 | a0001c0001t0005a0001c0001t0014a0001c0001t0022 | 15 | HG00621.hp1 HG00642.hp1 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2497A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 2497 | chr4 | 70984554 | |||||
| chr4:70984636
|
C | T | 1 | a0001c0001t0021 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2579C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 2579 | chr4 | 70984636 | |||||
| chr4:70984763
|
T | C | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2706T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 2706 | chr4 | 70984763 | |||||
| chr4:70984971
|
A | G | 1 | a0001c0001t0017 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2914A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 2914 | chr4 | 70984971 | |||||
| chr4:70985074
|
G | A | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3017G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 3017 | chr4 | 70985074 | |||||
| chr4:70985578
|
C | T | 2 | a0001c0001t0018a0001c0001t0023 | 2 | HG01891.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3521C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 3521 | chr4 | 70985578 | |||||
| chr4:70985692
|
A | G | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3635A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 3635 | chr4 | 70985692 | |||||
| chr4:70985823
|
A | G | 1 | a0001c0001t0022 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3766A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 3766 | chr4 | 70985823 | |||||
| chr4:70985959
|
A | C | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(24): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*3902A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 3902 | chr4 | 70985959 | |||||
| chr4:70986084
|
A | G | 1 | a0001c0001t0012 | 2 | HG02132.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4027A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4027 | chr4 | 70986084 | |||||
| chr4:70986251
|
C | T | 1 | a0001c0001t0026 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4194C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4194 | chr4 | 70986251 | |||||
| chr4:70986441
|
A | T | 1 | a0001c0001t0020 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4384A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4384 | chr4 | 70986441 | |||||
| chr4:70986693
|
G | A | 11 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(8): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*4636G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4636 | chr4 | 70986693 | |||||
| chr4:70986786
|
T | G | 2 | a0001c0001t0018a0001c0001t0023 | 2 | HG01891.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4729T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4729 | chr4 | 70986786 | |||||
| chr4:70986820
|
T | A | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4763T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4763 | chr4 | 70986820 | |||||
| chr4:70986823
|
A | G | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4766A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 4766 | chr4 | 70986823 | |||||
| chr4:70987213
|
T | A | 2 | a0001c0001t0019a0001c0001t0024 | 2 | HG02602.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5156T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 5156 | chr4 | 70987213 | |||||
| chr4:70987278
|
C | T | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5221C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 5221 | chr4 | 70987278 | |||||
| chr4:70987486
|
T | C | 1 | a0001c0001t0025 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5429T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 5429 | chr4 | 70987486 | |||||
| chr4:70987916
|
A | G | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5859A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 5859 | chr4 | 70987916 | |||||
| chr4:70988095
|
GT | G | 2 | a0001c0001t0007a0001c0001t0015 | 8 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6051delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 6/6 | 6051 | INFO_REALIGN_3_PRIME | chr4 | 70988095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70902602
|
C | CCCGCCCG | 64 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0002g0004others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.14+67_14+73dupCCGC others(3): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70902602 | |||||
| chr4:70902602
|
CCCGCCCG | C | 19 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(16): Show | 19 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+67_14+73delCCGC others(3): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70902602 | |||||
| chr4:70902801
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.14+251C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70902801 | ||||||
| chr4:70902842
|
C | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+292C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70902842 | ||||||
| chr4:70902870
|
T | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+320T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70902870 | ||||||
| chr4:70903042
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.14+492C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70903042 | ||||||
| chr4:70903176
|
A | G | 3 | a0001c0001t0008g0262a0001c0001t0008g0263a0001c0001t0008g0264 | 3 | HG02717.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.14+626A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70903176 | ||||||
| chr4:70903213
|
T | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+663T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70903213 | ||||||
| chr4:70903597
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+1047T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70903597 | ||||||
| chr4:70903792
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0020g0261 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.14+1242A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70903792 | ||||||
| chr4:70903906
|
G | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14+1356G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70903906 | ||||||
| chr4:70903945
|
T | TAAAAAAG others(346): Show |
1 | a0001c0001t0004g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.14+1406_14+1407ins others(353): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70903945 | |||||
| chr4:70903974
|
C | CT | 68 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0077others(65): Show | 68 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.14+1448dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70903974 | |||||
| chr4:70903974
|
C | CTT | 152 | a0001c0001t0001g0054a0001c0001t0001g0066a0001c0001t0001g0098others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.14+1447_14+1448dup others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70903974 | |||||
| chr4:70903974
|
C | CTTT | 37 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0230others(34): Show | 38 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.14+1446_14+1448dup others(3): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70903974 | |||||
| chr4:70904029
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0098 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.14+1479G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904029 | ||||||
| chr4:70904349
|
C | G | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+1799C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904349 | ||||||
| chr4:70904498
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.14+1948T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904498 | ||||||
| chr4:70904584
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.14+2034C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904584 | ||||||
| chr4:70904716
|
G | A | 1 | a0001c0001t0004g0282 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.14+2166G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904716 | ||||||
| chr4:70904758
|
C | CA | 16 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0100others(13): Show | 16 | HG00609.hp2 HG01243.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.14+2226dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70904758 | |||||
| chr4:70904758
|
CA | C | 23 | a0001c0001t0001g0071a0001c0001t0002g0048a0001c0001t0004g0267others(20): Show | 23 | HG01243.hp2 HG01891.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+2226delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70904758 | |||||
| chr4:70904773
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.14+2223A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904773 | ||||||
| chr4:70904802
|
T | TGG | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+2253_14+2254dup others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70904802 | |||||
| chr4:70904867
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.14+2317T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904867 | ||||||
| chr4:70904995
|
C | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+2445C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70904995 | ||||||
| chr4:70905004
|
G | T | 1 | a0001c0001t0004g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.14+2454G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905004 | ||||||
| chr4:70905037
|
C | T | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG01258.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+2487C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905037 | ||||||
| chr4:70905046
|
T | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01433.hp2 HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.14+2496T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905046 | ||||||
| chr4:70905047
|
A | G | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+2497A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905047 | ||||||
| chr4:70905136
|
A | T | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+2586A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905136 | ||||||
| chr4:70905192
|
T | C | 4 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0081others(1): Show | 4 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+2642T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905192 | ||||||
| chr4:70905207
|
A | G | 2 | a0001c0001t0004g0273a0001c0001t0004g0282 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.14+2657A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905207 | ||||||
| chr4:70905275
|
G | A | 6 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(3): Show | 6 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+2725G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905275 | ||||||
| chr4:70905279
|
A | G | 1 | a0001c0001t0004g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.14+2729A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905279 | ||||||
| chr4:70905429
|
G | T | 6 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(3): Show | 6 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+2879G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905429 | ||||||
| chr4:70906009
|
C | T | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+3459C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906009 | ||||||
| chr4:70906046
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.14+3496T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906046 | ||||||
| chr4:70906099
|
G | A | 1 | a0001c0001t0003g0082 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.14+3549G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906099 | ||||||
| chr4:70906234
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0066others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.14+3684C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906234 | ||||||
| chr4:70906387
|
A | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0042others(5): Show | 8 | NA18942.hp2 NA18955.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.14+3837A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906387 | ||||||
| chr4:70906517
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.14+3967G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906517 | ||||||
| chr4:70906541
|
A | G | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+3991A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906541 | ||||||
| chr4:70906769
|
A | G | 1 | a0001c0001t0004g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.14+4219A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906769 | ||||||
| chr4:70906922
|
A | G | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+4372A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70906922 | ||||||
| chr4:70907371
|
T | C | 2 | a0001c0001t0003g0221a0001c0001t0003g0222 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.14+4821T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70907371 | ||||||
| chr4:70907453
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+4903C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70907453 | ||||||
| chr4:70907495
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.14+4945G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70907495 | ||||||
| chr4:70907639
|
G | A | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+5089G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70907639 | ||||||
| chr4:70907760
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.14+5210C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70907760 | ||||||
| chr4:70908014
|
A | G | 14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.14+5464A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908014 | ||||||
| chr4:70908029
|
C | CT | 12 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(9): Show | 12 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.14+5493dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70908029 | |||||
| chr4:70908057
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14+5507G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908057 | ||||||
| chr4:70908064
|
C | T | 4 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0081others(1): Show | 4 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+5514C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908064 | ||||||
| chr4:70908086
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0013g0211 | 2 | HG02258.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.14+5536C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908086 | ||||||
| chr4:70908114
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.14+5564C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908114 | ||||||
| chr4:70908146
|
C | T | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+5596C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908146 | ||||||
| chr4:70908330
|
CT | C | 11 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | NA18941.hp1 NA18941.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+5796delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70908330 | |||||
| chr4:70908398
|
A | G | 2 | a0001c0001t0006g0053a0001c0001t0006g0061 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.14+5848A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908398 | ||||||
| chr4:70908459
|
C | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14+5909C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908459 | ||||||
| chr4:70908618
|
C | CA | 7 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(4): Show | 7 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+6075dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70908618 | |||||
| chr4:70908623
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.14+6073A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908623 | ||||||
| chr4:70908630
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(244): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.14+6080T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908630 | ||||||
| chr4:70908709
|
A | C | 1 | a0001c0001t0007g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.14+6159A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908709 | ||||||
| chr4:70908769
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.14+6219C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908769 | ||||||
| chr4:70908774
|
TA | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(272): Show | 276 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.14+6236delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70908774 | |||||
| chr4:70908774
|
TAA | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG00140.hp2 HG01433.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+6235_14+6236del others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70908774 | |||||
| chr4:70908878
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+6328C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908878 | ||||||
| chr4:70908893
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.14+6343T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908893 | ||||||
| chr4:70908982
|
C | T | 15 | a0001c0001t0005g0078a0001c0001t0005g0102a0001c0001t0005g0103others(12): Show | 15 | HG00621.hp1 HG00642.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+6432C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70908982 | ||||||
| chr4:70909029
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG02083.hp1 HG02280.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+6479C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70909029 | ||||||
| chr4:70909050
|
C | CA | 30 | a0001c0001t0001g0066a0001c0001t0001g0112a0001c0001t0001g0113others(27): Show | 30 | HG00597.hp1 HG01261.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.14+6517dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70909050 | |||||
| chr4:70909050
|
CA | C | 7 | a0001c0001t0001g0054a0001c0001t0001g0196a0001c0001t0001g0197others(4): Show | 7 | HG01168.hp2 HG02280.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+6517delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70909050 | |||||
| chr4:70909069
|
T | C | 1 | a0001c0001t0005g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.14+6519T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70909069 | ||||||
| chr4:70909107
|
T | TTGTA | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+6560_14+6561ins others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70909107 | |||||
| chr4:70909219
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+6669C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70909219 | ||||||
| chr4:70909680
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.14+7130A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70909680 | ||||||
| chr4:70909732
|
C | CT | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+7194dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70909732 | |||||
| chr4:70909820
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.14+7270G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70909820 | ||||||
| chr4:70910187
|
T | C | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+7637T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70910187 | ||||||
| chr4:70910206
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.14+7656A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70910206 | ||||||
| chr4:70910383
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.14+7833C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70910383 | ||||||
| chr4:70910477
|
A | T | 47 | a0001c0001t0001g0193a0001c0001t0002g0004a0001c0001t0002g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.14+7927A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70910477 | ||||||
| chr4:70910605
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+8055G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70910605 | ||||||
| chr4:70910699
|
C | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(181): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.14+8149C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70910699 | ||||||
| chr4:70911005
|
C | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+8455C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911005 | ||||||
| chr4:70911075
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(147): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.14+8525C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911075 | ||||||
| chr4:70911218
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0068others(80): Show | 84 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.14+8668A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911218 | ||||||
| chr4:70911304
|
A | C | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+8754A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911304 | ||||||
| chr4:70911471
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+8921G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911471 | ||||||
| chr4:70911581
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+9031T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911581 | ||||||
| chr4:70911769
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.14+9219A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911769 | ||||||
| chr4:70911857
|
C | T | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+9307C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911857 | ||||||
| chr4:70911858
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.14+9308G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911858 | ||||||
| chr4:70911897
|
C | CT | 9 | a0001c0001t0001g0191a0001c0001t0001g0243a0001c0001t0001g0254others(6): Show | 9 | HG01109.hp2 HG02056.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+9364dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70911897 | |||||
| chr4:70911897
|
CT | C | 8 | a0001c0001t0001g0073a0001c0001t0001g0121a0001c0001t0002g0017others(5): Show | 8 | HG01928.hp2 HG02717.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+9364delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70911897 | |||||
| chr4:70911968
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+9418C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911968 | ||||||
| chr4:70912087
|
G | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+9537G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912087 | ||||||
| chr4:70912176
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0020g0261 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.14+9626C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912176 | ||||||
| chr4:70912177
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+9627G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912177 | ||||||
| chr4:70912225
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+9675T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912225 | ||||||
| chr4:70912283
|
AT | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(243): Show | 247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.14+9747delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70912283 | |||||
| chr4:70912329
|
G | C | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+9779G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912329 | ||||||
| chr4:70912333
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+9783G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912333 | ||||||
| chr4:70912436
|
C | A | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+9886C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912436 | ||||||
| chr4:70912659
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.14+10109C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912659 | ||||||
| chr4:70912728
|
T | A | 57 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.14+10178T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912728 | ||||||
| chr4:70912836
|
C | T | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+10286C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70912836 | ||||||
| chr4:70913099
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+10549C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70913099 | ||||||
| chr4:70913259
|
G | GGTAT | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0242others(2): Show | 5 | HG00621.hp1 HG02129.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+10750_14+10753d others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70913259 | |||||
| chr4:70913259
|
GGTAT | G | 75 | a0001c0001t0001g0100a0001c0001t0001g0123a0001c0001t0001g0124others(72): Show | 75 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.14+10750_14+10753d others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70913259 | |||||
| chr4:70913259
|
GGTATGTA others(5): Show |
G | 12 | a0001c0001t0001g0066a0001c0001t0001g0112a0001c0001t0001g0113others(9): Show | 12 | HG00597.hp1 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.14+10742_14+10753d others(14): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70913259 | |||||
| chr4:70913259
|
GGTATGTA others(9): Show |
G | 1 | a0001c0001t0003g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.14+10738_14+10753d others(18): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70913259 | |||||
| chr4:70913304
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.14+10754C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70913304 | ||||||
| chr4:70913317
|
G | C | 15 | a0001c0001t0002g0009a0001c0001t0006g0047a0001c0001t0006g0049others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+10767G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70913317 | ||||||
| chr4:70913618
|
T | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+11068T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70913618 | ||||||
| chr4:70913635
|
C | T | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+11085C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70913635 | ||||||
| chr4:70913918
|
C | CT | 166 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.14+11379dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70913918 | |||||
| chr4:70914177
|
A | T | 5 | a0001c0001t0003g0076a0001c0001t0003g0089a0001c0001t0003g0095others(2): Show | 5 | HG03710.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+11627A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70914177 | ||||||
| chr4:70914376
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.14+11826A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70914376 | ||||||
| chr4:70914387
|
CT | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+11839delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70914387 | |||||
| chr4:70914447
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.14+11897A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70914447 | ||||||
| chr4:70914789
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+12239C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70914789 | ||||||
| chr4:70914858
|
T | C | 5 | a0001c0001t0004g0069a0001c0001t0004g0079a0001c0001t0004g0080others(2): Show | 5 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+12308T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70914858 | ||||||
| chr4:70914922
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.14+12372G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70914922 | ||||||
| chr4:70915047
|
A | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14+12497A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915047 | ||||||
| chr4:70915056
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.14+12506C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915056 | ||||||
| chr4:70915101
|
T | C | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+12551T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915101 | ||||||
| chr4:70915176
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.14+12626T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915176 | ||||||
| chr4:70915271
|
A | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG00140.hp1 HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.14+12721A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915271 | ||||||
| chr4:70915469
|
C | T | 28 | a0001c0001t0001g0077a0001c0001t0001g0117a0001c0001t0001g0121others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.14+12919C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915469 | ||||||
| chr4:70915714
|
C | A | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+13164C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915714 | ||||||
| chr4:70915905
|
CTTAAGT | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+13358_14+13363d others(8): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70915905 | |||||
| chr4:70915964
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+13414G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70915964 | ||||||
| chr4:70916019
|
C | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.14+13469C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916019 | ||||||
| chr4:70916120
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14+13570G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916120 | ||||||
| chr4:70916410
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.14+13860G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916410 | ||||||
| chr4:70916473
|
C | T | 7 | a0001c0001t0006g0047a0001c0001t0006g0053a0001c0001t0006g0057others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+13923C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916473 | ||||||
| chr4:70916602
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0149a0001c0001t0001g0197 | 3 | HG02559.hp2 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.14+14052A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916602 | ||||||
| chr4:70916621
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.14+14071G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916621 | ||||||
| chr4:70916692
|
C | T | 7 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(4): Show | 7 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+14142C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916692 | ||||||
| chr4:70916783
|
C | G | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+14233C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916783 | ||||||
| chr4:70916838
|
G | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+14288G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70916838 | ||||||
| chr4:70917193
|
T | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14+14643T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917193 | ||||||
| chr4:70917212
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+14662C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917212 | ||||||
| chr4:70917276
|
G | C | 9 | a0001c0001t0003g0075a0001c0001t0003g0082a0001c0001t0003g0088others(6): Show | 9 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+14726G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917276 | ||||||
| chr4:70917381
|
G | T | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+14831G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917381 | ||||||
| chr4:70917407
|
T | G | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+14857T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917407 | ||||||
| chr4:70917501
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.14+14951T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917501 | ||||||
| chr4:70917805
|
G | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(182): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.14+15255G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917805 | ||||||
| chr4:70917877
|
A | G | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+15327A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917877 | ||||||
| chr4:70917880
|
A | C | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.14+15330A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70917880 | ||||||
| chr4:70917921
|
A | ATATC | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+15372_14+15373i others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70917921 | |||||
| chr4:70918197
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0068others(79): Show | 83 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.14+15647G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918197 | ||||||
| chr4:70918475
|
G | C | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+15925G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918475 | ||||||
| chr4:70918481
|
A | G | 1 | a0001c0001t0002g0031 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.14+15931A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918481 | ||||||
| chr4:70918504
|
G | A | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+15954G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918504 | ||||||
| chr4:70918570
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0253 | 2 | HG00735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.14+16020A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918570 | ||||||
| chr4:70918571
|
T | C | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+16021T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918571 | ||||||
| chr4:70918597
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0048 | 2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.14+16047G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918597 | ||||||
| chr4:70918652
|
C | T | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+16102C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918652 | ||||||
| chr4:70918701
|
T | A | 2 | a0001c0001t0010g0006a0001c0001t0010g0015 | 2 | NA18968.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.14+16151T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918701 | ||||||
| chr4:70918874
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.14+16324C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70918874 | ||||||
| chr4:70919020
|
A | G | 2 | a0001c0001t0007g0278a0001c0001t0007g0281 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.14+16470A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919020 | ||||||
| chr4:70919315
|
TA | T | 20 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(17): Show | 20 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.14+16778delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70919315 | |||||
| chr4:70919342
|
C | T | 6 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(3): Show | 6 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+16792C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919342 | ||||||
| chr4:70919437
|
C | T | 1 | a0001c0002t0006g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14+16887C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919437 | ||||||
| chr4:70919520
|
A | C | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+16970A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919520 | ||||||
| chr4:70919563
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0020g0261 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.14+17013A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919563 | ||||||
| chr4:70919596
|
T | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+17046T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919596 | ||||||
| chr4:70919646
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.14+17096G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919646 | ||||||
| chr4:70919661
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.14+17111G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919661 | ||||||
| chr4:70919678
|
T | C | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+17128T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919678 | ||||||
| chr4:70919864
|
A | T | 1 | a0001c0002t0006g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14+17314A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919864 | ||||||
| chr4:70919866
|
G | A | 1 | a0001c0001t0026g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+17316G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70919866 | ||||||
| chr4:70920165
|
C | T | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+17615C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920165 | ||||||
| chr4:70920247
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.14+17697C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920247 | ||||||
| chr4:70920253
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.14+17703C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920253 | ||||||
| chr4:70920377
|
G | A | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+17827G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920377 | ||||||
| chr4:70920426
|
T | C | 9 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(6): Show | 9 | HG02615.hp2 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+17876T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920426 | ||||||
| chr4:70920558
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.14+18008T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920558 | ||||||
| chr4:70920559
|
G | A | 28 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(25): Show | 28 | HG00673.hp1 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+18009G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920559 | ||||||
| chr4:70920573
|
G | A | 1 | a0001c0001t0011g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.14+18023G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920573 | ||||||
| chr4:70920574
|
T | C | 1 | a0001c0001t0024g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.14+18024T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920574 | ||||||
| chr4:70920689
|
T | C | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+18139T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920689 | ||||||
| chr4:70920890
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0136a0001c0001t0001g0238 | 3 | HG01167.hp2 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.14+18340G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920890 | ||||||
| chr4:70920994
|
T | A | 15 | a0001c0001t0002g0009a0001c0001t0006g0047a0001c0001t0006g0049others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+18444T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70920994 | ||||||
| chr4:70921067
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.14+18517A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921067 | ||||||
| chr4:70921078
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+18528A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921078 | ||||||
| chr4:70921266
|
C | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0242 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.14+18716C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921266 | ||||||
| chr4:70921446
|
G | A | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+18896G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921446 | ||||||
| chr4:70921476
|
T | TCTCCCCT others(3): Show |
1 | a0001c0001t0001g0244 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.14+18928_14+18929i others(12): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921476 | |||||
| chr4:70921479
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0244 | 2 | HG01978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.14+18929T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921479 | ||||||
| chr4:70921481
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0244 | 2 | HG01978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.14+18931T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921481 | ||||||
| chr4:70921481
|
T | TCTCCC | 29 | a0001c0001t0001g0077a0001c0001t0001g0117a0001c0001t0001g0121others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.14+18959_14+18963d others(7): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921481 | |||||
| chr4:70921481
|
T | TCTCCCCT others(3): Show |
174 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0066others(171): Show | 175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.14+18954_14+18963d others(12): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921481 | |||||
| chr4:70921481
|
T | TCTCCCCT others(8): Show |
12 | a0001c0001t0001g0054a0001c0001t0001g0120a0001c0001t0001g0128others(9): Show | 12 | HG00438.hp2 HG01361.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.14+18949_14+18963d others(17): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921481 | |||||
| chr4:70921481
|
T | TCTCCCCT others(9): Show |
1 | a0001c0001t0001g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.14+18932_14+18947d others(18): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921481 | |||||
| chr4:70921481
|
T | TCTCCCCT others(13): Show |
7 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+18944_14+18963d others(22): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921481 | |||||
| chr4:70921481
|
TCTCCCCT others(8): Show |
T | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+18949_14+18963d others(17): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921481 | |||||
| chr4:70921482
|
C | CTCCCCTC others(8): Show |
2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14+18946_14+18947i others(17): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921482 | |||||
| chr4:70921487
|
C | CTCCCCTC others(3): Show |
4 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0234others(1): Show | 4 | HG03492.hp2 HG04115.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+18946_14+18947i others(12): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921487 | |||||
| chr4:70921488
|
T | TCCCCTCC others(4): Show |
1 | a0001c0001t0001g0073 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.14+18942_14+18952d others(13): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921488 | |||||
| chr4:70921499
|
C | CCCCTCCC others(8): Show |
9 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(6): Show | 9 | HG02615.hp2 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+18954_14+18968d others(17): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70921499 | |||||
| chr4:70921499
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14+18949C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921499 | ||||||
| chr4:70921514
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.14+18964T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921514 | ||||||
| chr4:70921597
|
G | A | 4 | a0001c0001t0008g0010a0001c0001t0008g0084a0001c0001t0008g0224others(1): Show | 4 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+19047G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921597 | ||||||
| chr4:70921613
|
A | G | 15 | a0001c0001t0002g0009a0001c0001t0006g0047a0001c0001t0006g0049others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+19063A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921613 | ||||||
| chr4:70921628
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+19078G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921628 | ||||||
| chr4:70921677
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.14+19127T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921677 | ||||||
| chr4:70921701
|
G | T | 1 | a0001c0001t0003g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14+19151G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921701 | ||||||
| chr4:70921755
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.14+19205C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921755 | ||||||
| chr4:70921801
|
C | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.14+19251C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921801 | ||||||
| chr4:70921874
|
A | G | 1 | a0001c0001t0011g0265 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.14+19324A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921874 | ||||||
| chr4:70921893
|
A | G | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+19343A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921893 | ||||||
| chr4:70921944
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.14+19394C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70921944 | ||||||
| chr4:70922144
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0021 | 3 | NA18982.hp1 NA19065.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.14+19594T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922144 | ||||||
| chr4:70922371
|
A | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0038a0001c0001t0002g0048 | 3 | HG01975.hp1 HG01993.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.14+19821A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922371 | ||||||
| chr4:70922526
|
G | T | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+19976G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922526 | ||||||
| chr4:70922589
|
G | A | 1 | a0001c0001t0014g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.14+20039G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922589 | ||||||
| chr4:70922692
|
T | G | 3 | a0001c0001t0008g0262a0001c0001t0008g0263a0001c0001t0008g0264 | 3 | HG02717.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.14+20142T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922692 | ||||||
| chr4:70922704
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+20154T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922704 | ||||||
| chr4:70922829
|
G | A | 18 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.14+20279G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70922829 | ||||||
| chr4:70923023
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.14+20473A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923023 | ||||||
| chr4:70923158
|
G | A | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+20608G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923158 | ||||||
| chr4:70923355
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.14+20805G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923355 | ||||||
| chr4:70923452
|
C | T | 11 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+20902C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923452 | ||||||
| chr4:70923480
|
G | A | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+20930G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923480 | ||||||
| chr4:70923546
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.14+20996T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923546 | ||||||
| chr4:70923678
|
G | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14+21128G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923678 | ||||||
| chr4:70923777
|
C | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.14+21227C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923777 | ||||||
| chr4:70923940
|
C | CA | 99 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0001g0186others(96): Show | 99 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.14+21407dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70923940 | |||||
| chr4:70923940
|
CA | C | 38 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0117others(35): Show | 38 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.14+21407delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70923940 | |||||
| chr4:70923959
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.14+21409T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70923959 | ||||||
| chr4:70923965
|
C | CA | 178 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(175): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.14+21428dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70923965 | |||||
| chr4:70923965
|
C | CAA | 91 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(88): Show | 91 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.14+21427_14+21428d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70923965 | |||||
| chr4:70924026
|
A | G | 5 | a0001c0001t0004g0069a0001c0001t0004g0079a0001c0001t0004g0080others(2): Show | 5 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+21476A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924026 | ||||||
| chr4:70924056
|
A | G | 7 | a0001c0001t0006g0047a0001c0001t0006g0053a0001c0001t0006g0057others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+21506A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924056 | ||||||
| chr4:70924091
|
A | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+21541A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924091 | ||||||
| chr4:70924127
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.14+21577C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924127 | ||||||
| chr4:70924524
|
G | A | 14 | a0001c0001t0001g0054a0001c0001t0001g0156a0001c0001t0001g0157others(11): Show | 14 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.14+21974G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924524 | ||||||
| chr4:70924568
|
G | C | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+22018G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924568 | ||||||
| chr4:70924665
|
A | G | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+22115A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924665 | ||||||
| chr4:70924755
|
C | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+22205C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924755 | ||||||
| chr4:70924952
|
G | A | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+22402G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70924952 | ||||||
| chr4:70925087
|
A | C | 1 | a0001c0001t0005g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.14+22537A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925087 | ||||||
| chr4:70925416
|
A | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0225 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.14+22866A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925416 | ||||||
| chr4:70925434
|
A | T | 1 | a0001c0001t0016g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+22884A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925434 | ||||||
| chr4:70925530
|
G | C | 9 | a0001c0001t0001g0066a0001c0001t0001g0112a0001c0001t0001g0113others(6): Show | 9 | HG00597.hp1 HG02074.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+22980G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925530 | ||||||
| chr4:70925560
|
A | G | 1 | a0001c0001t0005g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.14+23010A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925560 | ||||||
| chr4:70925576
|
T | C | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+23026T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925576 | ||||||
| chr4:70925739
|
G | A | 1 | a0001c0001t0003g0082 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.14+23189G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925739 | ||||||
| chr4:70925766
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.14+23216C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925766 | ||||||
| chr4:70925785
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(55): Show | 58 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.14+23235C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925785 | ||||||
| chr4:70925885
|
T | C | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+23335T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70925885 | ||||||
| chr4:70926071
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.14+23521T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926071 | ||||||
| chr4:70926086
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.14+23536C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926086 | ||||||
| chr4:70926131
|
G | A | 3 | a0001c0001t0008g0010a0001c0001t0008g0084a0001c0001t0008g0224 | 3 | HG01167.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.14+23581G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926131 | ||||||
| chr4:70926208
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14+23658C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926208 | ||||||
| chr4:70926264
|
A | AT | 15 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0131others(12): Show | 15 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.14+23730dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70926264 | |||||
| chr4:70926264
|
A | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14+23714A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926264 | ||||||
| chr4:70926280
|
T | A | 2 | a0001c0001t0001g0260a0001c0001t0020g0261 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.14+23730T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926280 | ||||||
| chr4:70926548
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.14+23998C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926548 | ||||||
| chr4:70926626
|
A | G | 28 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0105others(25): Show | 28 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+24076A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926626 | ||||||
| chr4:70926628
|
G | T | 42 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.14+24078G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926628 | ||||||
| chr4:70926778
|
T | C | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(55): Show | 58 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.14+24228T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926778 | ||||||
| chr4:70926804
|
G | A | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+24254G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926804 | ||||||
| chr4:70926820
|
C | T | 1 | a0001c0001t0005g0208 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.14+24270C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926820 | ||||||
| chr4:70926858
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+24308G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926858 | ||||||
| chr4:70926914
|
G | A | 9 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+24364G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926914 | ||||||
| chr4:70926916
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(249): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.14+24366A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926916 | ||||||
| chr4:70926926
|
G | C | 1 | a0001c0001t0005g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14+24376G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70926926 | ||||||
| chr4:70927003
|
G | GA | 236 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(233): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.14+24466dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70927003 | |||||
| chr4:70927124
|
G | A | 1 | a0001c0001t0005g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14+24574G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927124 | ||||||
| chr4:70927323
|
G | C | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+24773G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927323 | ||||||
| chr4:70927336
|
C | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+24786C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927336 | ||||||
| chr4:70927394
|
G | A | 1 | a0001c0001t0021g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.14+24844G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927394 | ||||||
| chr4:70927539
|
C | CA | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+25002dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70927539 | |||||
| chr4:70927539
|
CA | C | 23 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(20): Show | 23 | HG00673.hp1 HG01123.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+25002delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70927539 | |||||
| chr4:70927580
|
T | C | 2 | a0001c0001t0003g0221a0001c0001t0003g0222 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.14+25030T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927580 | ||||||
| chr4:70927649
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(249): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.14+25099T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927649 | ||||||
| chr4:70927668
|
A | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+25118A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927668 | ||||||
| chr4:70927671
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.14+25121C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927671 | ||||||
| chr4:70927673
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.14+25123G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927673 | ||||||
| chr4:70927767
|
C | T | 20 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(17): Show | 20 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.14+25217C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927767 | ||||||
| chr4:70927858
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.14+25308G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927858 | ||||||
| chr4:70927859
|
C | G | 1 | a0001c0001t0002g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.14+25309C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927859 | ||||||
| chr4:70927977
|
T | C | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+25427T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70927977 | ||||||
| chr4:70928299
|
G | GT | 7 | a0001c0001t0001g0068a0001c0001t0001g0183a0001c0001t0002g0029others(4): Show | 7 | HG02738.hp1 HG02738.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+25763dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70928299 | |||||
| chr4:70928364
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+25814C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70928364 | ||||||
| chr4:70928380
|
C | G | 10 | a0001c0001t0001g0066a0001c0001t0001g0112a0001c0001t0001g0113others(7): Show | 10 | HG00597.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.14+25830C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70928380 | ||||||
| chr4:70928412
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.14+25862C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70928412 | ||||||
| chr4:70928932
|
T | C | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.14+26382T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70928932 | ||||||
| chr4:70928966
|
A | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+26416A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70928966 | ||||||
| chr4:70928997
|
C | T | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.14+26447C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70928997 | ||||||
| chr4:70929045
|
T | G | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.14+26495T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929045 | ||||||
| chr4:70929163
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.14+26613C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929163 | ||||||
| chr4:70929174
|
C | CTTCTTTT others(3): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0195 | 2 | HG02451.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.14+26626_14+26627i others(12): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70929174 | |||||
| chr4:70929182
|
CT | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.14+26650delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70929182 | |||||
| chr4:70929182
|
CTT | C | 8 | a0001c0001t0001g0098a0001c0001t0001g0137a0001c0001t0002g0004others(5): Show | 8 | HG01891.hp2 HG01975.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+26649_14+26650d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70929182 | |||||
| chr4:70929190
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+26640T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929190 | ||||||
| chr4:70929282
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0021 | 2 | NA18982.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.14+26732G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929282 | ||||||
| chr4:70929339
|
C | T | 9 | a0001c0001t0003g0085a0001c0001t0003g0225a0001c0001t0007g0275others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+26789C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929339 | ||||||
| chr4:70929420
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.14+26870C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929420 | ||||||
| chr4:70929518
|
T | A | 1 | a0001c0002t0006g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14+26968T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929518 | ||||||
| chr4:70929545
|
A | G | 1 | a0001c0001t0005g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.14+26995A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929545 | ||||||
| chr4:70929629
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.14+27079C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929629 | ||||||
| chr4:70929647
|
AT | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0131a0001c0001t0001g0153others(3): Show | 6 | HG02155.hp2 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+27113delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70929647 | |||||
| chr4:70929677
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.14+27127A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929677 | ||||||
| chr4:70929684
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+27134C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929684 | ||||||
| chr4:70929794
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.14+27244C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929794 | ||||||
| chr4:70929868
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.14+27318T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929868 | ||||||
| chr4:70929879
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG01891.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+27329C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929879 | ||||||
| chr4:70929906
|
T | C | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+27356T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929906 | ||||||
| chr4:70929983
|
G | C | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14+27433G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70929983 | ||||||
| chr4:70930071
|
A | C | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.14+27521A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930071 | ||||||
| chr4:70930196
|
A | G | 1 | a0001c0001t0006g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.14+27646A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930196 | ||||||
| chr4:70930215
|
T | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0225 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.14+27665T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930215 | ||||||
| chr4:70930345
|
T | A | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14+27795T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930345 | ||||||
| chr4:70930359
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.14+27809T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930359 | ||||||
| chr4:70930449
|
T | A | 1 | a0001c0001t0004g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.14+27899T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930449 | ||||||
| chr4:70930483
|
C | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.14+27933C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930483 | ||||||
| chr4:70930498
|
G | A | 1 | a0001c0001t0008g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14+27948G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930498 | ||||||
| chr4:70930536
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.14+27986T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70930536 | ||||||
| chr4:70930965
|
C | CT | 33 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0088others(30): Show | 33 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(30): Show |
intron_variant | MODIFIER | c.15-27888dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70930965 | |||||
| chr4:70930965
|
CT | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0066others(158): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.15-27888delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70930965 | |||||
| chr4:70930965
|
CTT | C | 9 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | HG01070.hp1 HG01070.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.15-27889_15-27888d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70930965 | |||||
| chr4:70931259
|
A | G | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.15-27615A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931259 | ||||||
| chr4:70931422
|
A | G | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.15-27452A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931422 | ||||||
| chr4:70931655
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-27219G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931655 | ||||||
| chr4:70931746
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0020g0261 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.15-27128C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931746 | ||||||
| chr4:70931753
|
C | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-27121C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931753 | ||||||
| chr4:70931918
|
C | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-26956C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931918 | ||||||
| chr4:70931930
|
G | T | 3 | a0001c0001t0005g0103a0001c0001t0005g0201a0001c0001t0005g0208 | 3 | HG00642.hp1 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.15-26944G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70931930 | ||||||
| chr4:70932122
|
A | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-26752A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932122 | ||||||
| chr4:70932189
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.15-26685A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932189 | ||||||
| chr4:70932218
|
A | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-26656A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932218 | ||||||
| chr4:70932323
|
C | A | 1 | a0001c0001t0005g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.15-26551C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932323 | ||||||
| chr4:70932408
|
T | G | 7 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(4): Show | 7 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-26466T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932408 | ||||||
| chr4:70932409
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.15-26465T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932409 | ||||||
| chr4:70932447
|
T | A | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-26427T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932447 | ||||||
| chr4:70932453
|
T | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG00609.hp1 HG01433.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.15-26421T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932453 | ||||||
| chr4:70932937
|
G | A | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.15-25937G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70932937 | ||||||
| chr4:70933058
|
T | C | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-25816T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70933058 | ||||||
| chr4:70933238
|
G | A | 1 | a0001c0001t0007g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15-25636G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70933238 | ||||||
| chr4:70933259
|
A | G | 8 | a0001c0001t0001g0170a0001c0001t0004g0267a0001c0001t0004g0268others(5): Show | 8 | HG02486.hp2 HG02615.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-25615A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70933259 | ||||||
| chr4:70933280
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.15-25594C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70933280 | ||||||
| chr4:70933542
|
C | CT | 22 | a0001c0001t0001g0068a0001c0001t0001g0099a0001c0001t0001g0117others(19): Show | 22 | HG01433.hp1 HG02129.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.15-25305dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70933542 | |||||
| chr4:70933542
|
CT | C | 24 | a0001c0001t0001g0054a0001c0001t0001g0109a0001c0001t0001g0124others(21): Show | 24 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.15-25305delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70933542 | |||||
| chr4:70933542
|
CTT | C | 14 | a0001c0001t0004g0080a0001c0001t0004g0267a0001c0001t0004g0268others(11): Show | 14 | HG01515.hp2 HG02145.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.15-25306_15-25305d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70933542 | |||||
| chr4:70933542
|
CTTTTTTT others(2): Show |
C | 65 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.15-25313_15-25305d others(11): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70933542 | |||||
| chr4:70933612
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(242): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.15-25262T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70933612 | ||||||
| chr4:70933952
|
C | T | 16 | a0001c0001t0001g0107a0001c0001t0004g0067a0001c0001t0004g0069others(13): Show | 16 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.15-24922C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70933952 | ||||||
| chr4:70934292
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.15-24582G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70934292 | ||||||
| chr4:70934476
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-24398C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70934476 | ||||||
| chr4:70934481
|
C | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-24393C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70934481 | ||||||
| chr4:70934912
|
T | A | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.15-23962T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70934912 | ||||||
| chr4:70935026
|
C | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-23848C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935026 | ||||||
| chr4:70935035
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15-23839A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935035 | ||||||
| chr4:70935293
|
G | A | 1 | a0001c0001t0008g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.15-23581G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935293 | ||||||
| chr4:70935528
|
C | G | 1 | a0001c0001t0007g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15-23346C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935528 | ||||||
| chr4:70935577
|
T | G | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-23297T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935577 | ||||||
| chr4:70935601
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.15-23273G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935601 | ||||||
| chr4:70935655
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.15-23219T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935655 | ||||||
| chr4:70935747
|
C | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-23127C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935747 | ||||||
| chr4:70935778
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.15-23096C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70935778 | ||||||
| chr4:70935847
|
A | AT | 142 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0068others(139): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.15-23005dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70935847 | |||||
| chr4:70935847
|
A | ATT | 81 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0001g0108others(78): Show | 81 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.15-23006_15-23005d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70935847 | |||||
| chr4:70935847
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-23015_15-23005d others(13): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70935847 | |||||
| chr4:70935847
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0007g0276a0001c0001t0007g0280 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15-23016_15-23005d others(14): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70935847 | |||||
| chr4:70935847
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0007g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.15-23017_15-23005d others(15): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70935847 | |||||
| chr4:70935847
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-23016_15-23005d others(14): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70935847 | |||||
| chr4:70936098
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-22776G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936098 | ||||||
| chr4:70936102
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-22772C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936102 | ||||||
| chr4:70936129
|
G | T | 14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.15-22745G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936129 | ||||||
| chr4:70936175
|
G | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-22699G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936175 | ||||||
| chr4:70936511
|
C | T | 1 | a0001c0001t0005g0210 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.15-22363C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936511 | ||||||
| chr4:70936541
|
TTTTTGAC others(2481): Show |
T | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15-22332_15-19845d others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936541 | ||||||
| chr4:70936717
|
C | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-22157C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936717 | ||||||
| chr4:70936749
|
G | A | 2 | a0001c0001t0010g0006a0001c0001t0010g0015 | 2 | NA18968.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.15-22125G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936749 | ||||||
| chr4:70936925
|
T | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(233): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.15-21949T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70936925 | ||||||
| chr4:70937063
|
G | A | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-21811G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70937063 | ||||||
| chr4:70937516
|
G | GT | 14 | a0001c0001t0005g0210a0001c0001t0006g0047a0001c0001t0006g0049others(11): Show | 14 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.15-21349dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70937516 | |||||
| chr4:70937944
|
C | A | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-20930C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70937944 | ||||||
| chr4:70937997
|
C | T | 2 | a0001c0001t0004g0270a0001c0001t0004g0274 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.15-20877C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70937997 | ||||||
| chr4:70938030
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-20844G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938030 | ||||||
| chr4:70938098
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-20776G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938098 | ||||||
| chr4:70938313
|
G | GC | 5 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0154others(2): Show | 5 | HG00438.hp2 HG02080.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-20556dupC | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938313 | |||||
| chr4:70938319
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.15-20555G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938319 | ||||||
| chr4:70938319
|
G | GC | 16 | a0001c0001t0001g0160a0001c0001t0001g0242a0001c0001t0003g0082others(13): Show | 16 | HG00323.hp1 HG01071.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15-20540dupC | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938319 | |||||
| chr4:70938319
|
GC | G | 19 | a0001c0001t0001g0077a0001c0001t0001g0098a0001c0001t0001g0140others(16): Show | 19 | HG00673.hp1 HG01169.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.15-20540delC | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938319 | |||||
| chr4:70938333
|
C | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0217a0001c0001t0018g0002others(1): Show | 4 | HG01258.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-20541C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938333 | ||||||
| chr4:70938334
|
C | A | 70 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0101others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.15-20540C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938334 | ||||||
| chr4:70938334
|
C | CA | 70 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0066others(67): Show | 71 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.15-20525dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938334 | |||||
| chr4:70938334
|
C | CAA | 8 | a0001c0001t0001g0112a0001c0001t0001g0154a0001c0001t0001g0187others(5): Show | 8 | HG00438.hp2 HG01123.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-20526_15-20525d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938334 | |||||
| chr4:70938334
|
C | CCA | 40 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0129others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.15-20540_15-20539i others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938334 | ||||||
| chr4:70938335
|
A | C | 13 | a0001c0001t0001g0133a0001c0001t0003g0095a0001c0001t0003g0226others(10): Show | 13 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.15-20539A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938335 | ||||||
| chr4:70938336
|
A | C | 4 | a0001c0001t0007g0276a0001c0001t0007g0279a0001c0001t0011g0265others(1): Show | 4 | HG02559.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-20538A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938336 | ||||||
| chr4:70938337
|
A | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-20537A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938337 | ||||||
| chr4:70938573
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.15-20301G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938573 | ||||||
| chr4:70938710
|
TCCTAAAT others(1): Show |
T | 281 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.15-20155_15-20148d others(10): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938710 | |||||
| chr4:70938777
|
GT | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.15-20081delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938777 | |||||
| chr4:70938777
|
GTT | G | 56 | a0001c0001t0001g0132a0001c0001t0001g0163a0001c0001t0001g0198others(53): Show | 56 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-20082_15-20081d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70938777 | |||||
| chr4:70938792
|
T | G | 16 | a0001c0001t0002g0019a0001c0001t0005g0078a0001c0001t0005g0102others(13): Show | 16 | HG00621.hp1 HG00642.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.15-20082T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938792 | ||||||
| chr4:70938960
|
A | G | 31 | a0001c0001t0001g0077a0001c0001t0001g0112a0001c0001t0001g0117others(28): Show | 31 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.15-19914A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938960 | ||||||
| chr4:70938999
|
A | T | 1 | a0001c0001t0009g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.15-19875A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70938999 | ||||||
| chr4:70939031
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15-19843G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939031 | ||||||
| chr4:70939033
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15-19841G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939033 | ||||||
| chr4:70939093
|
G | C | 1 | a0001c0001t0004g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15-19781G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939093 | ||||||
| chr4:70939205
|
A | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-19669A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939205 | ||||||
| chr4:70939247
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA19005.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.15-19627C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939247 | ||||||
| chr4:70939288
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.15-19586A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939288 | ||||||
| chr4:70939349
|
T | C | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-19525T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939349 | ||||||
| chr4:70939640
|
A | G | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-19234A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939640 | ||||||
| chr4:70939654
|
C | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.15-19220C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939654 | ||||||
| chr4:70939659
|
G | A | 7 | a0001c0001t0006g0047a0001c0001t0006g0053a0001c0001t0006g0057others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-19215G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939659 | ||||||
| chr4:70939790
|
A | T | 2 | a0001c0001t0004g0273a0001c0001t0004g0282 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.15-19084A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939790 | ||||||
| chr4:70939945
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.15-18929G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70939945 | ||||||
| chr4:70940064
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.15-18810C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940064 | ||||||
| chr4:70940102
|
C | T | 2 | a0001c0001t0006g0064a0001c0001t0024g0063 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.15-18772C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940102 | ||||||
| chr4:70940201
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-18673C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940201 | ||||||
| chr4:70940301
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.15-18573C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940301 | ||||||
| chr4:70940349
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02056.hp2 NA19005.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.15-18525G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940349 | ||||||
| chr4:70940632
|
G | A | 16 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(13): Show | 16 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.15-18242G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940632 | ||||||
| chr4:70940672
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15-18202A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940672 | ||||||
| chr4:70940676
|
A | AT | 54 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0124others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.15-18181dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70940676 | |||||
| chr4:70940676
|
AT | A | 8 | a0001c0001t0001g0125a0001c0001t0001g0142a0001c0001t0001g0162others(5): Show | 8 | HG01070.hp1 HG01070.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-18181delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70940676 | |||||
| chr4:70940737
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-18137C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940737 | ||||||
| chr4:70940833
|
C | T | 1 | a0001c0001t0026g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-18041C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940833 | ||||||
| chr4:70940837
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.15-18037C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940837 | ||||||
| chr4:70940969
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.15-17905G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70940969 | ||||||
| chr4:70941160
|
C | CT | 8 | a0001c0001t0002g0056a0001c0001t0007g0275a0001c0001t0007g0276others(5): Show | 8 | HG00438.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-17699dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70941160 | |||||
| chr4:70941160
|
CT | C | 10 | a0001c0001t0001g0098a0001c0001t0001g0145a0001c0001t0001g0148others(7): Show | 10 | HG01517.hp1 HG01891.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.15-17699delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70941160 | |||||
| chr4:70941202
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-17672G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941202 | ||||||
| chr4:70941276
|
A | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-17598A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941276 | ||||||
| chr4:70941498
|
C | T | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.15-17376C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941498 | ||||||
| chr4:70941546
|
T | C | 1 | a0001c0001t0025g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.15-17328T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941546 | ||||||
| chr4:70941627
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(249): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.15-17247T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941627 | ||||||
| chr4:70941632
|
T | C | 19 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(16): Show | 19 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.15-17242T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941632 | ||||||
| chr4:70941671
|
G | T | 1 | a0001c0001t0001g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.15-17203G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941671 | ||||||
| chr4:70941754
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.15-17120C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941754 | ||||||
| chr4:70941986
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15-16888T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70941986 | ||||||
| chr4:70942101
|
A | G | 4 | a0001c0001t0007g0275a0001c0001t0007g0277a0001c0001t0007g0278others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-16773A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942101 | ||||||
| chr4:70942239
|
A | G | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.15-16635A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942239 | ||||||
| chr4:70942255
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.15-16619A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942255 | ||||||
| chr4:70942300
|
T | C | 1 | a0001c0001t0003g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-16574T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942300 | ||||||
| chr4:70942575
|
C | A | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-16299C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942575 | ||||||
| chr4:70942857
|
CAAAAT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.15-16013_15-16009d others(7): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70942857 | |||||
| chr4:70942975
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15-15899G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942975 | ||||||
| chr4:70942976
|
G | C | 17 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.15-15898G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70942976 | ||||||
| chr4:70943015
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.15-15859T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943015 | ||||||
| chr4:70943060
|
A | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-15814A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943060 | ||||||
| chr4:70943527
|
T | G | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-15347T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943527 | ||||||
| chr4:70943551
|
A | T | 1 | a0001c0001t0012g0175 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.15-15323A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943551 | ||||||
| chr4:70943842
|
T | G | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-15032T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943842 | ||||||
| chr4:70943880
|
A | C | 1 | a0001c0001t0003g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.15-14994A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943880 | ||||||
| chr4:70943881
|
C | A | 1 | a0001c0001t0006g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.15-14993C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70943881 | ||||||
| chr4:70944075
|
G | A | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-14799G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944075 | ||||||
| chr4:70944236
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.15-14638T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944236 | ||||||
| chr4:70944618
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.15-14256G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944618 | ||||||
| chr4:70944776
|
A | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0143 | 2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.15-14098A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944776 | ||||||
| chr4:70944788
|
T | C | 1 | a0001c0001t0009g0178 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.15-14086T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944788 | ||||||
| chr4:70944818
|
G | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-14056G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944818 | ||||||
| chr4:70944977
|
G | A | 28 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0099others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.15-13897G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70944977 | ||||||
| chr4:70945249
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.15-13625G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70945249 | ||||||
| chr4:70945719
|
A | C | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.15-13155A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70945719 | ||||||
| chr4:70945942
|
C | CT | 14 | a0001c0001t0001g0246a0001c0001t0006g0047a0001c0001t0006g0049others(11): Show | 14 | HG00597.hp2 HG01243.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.15-12921dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70945942 | |||||
| chr4:70946084
|
C | CTT | 6 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0278others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-12769_15-12768d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70946084 | |||||
| chr4:70946084
|
CT | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(209): Show | 213 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.15-12768delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70946084 | |||||
| chr4:70946287
|
A | G | 4 | a0001c0001t0008g0070a0001c0001t0008g0262a0001c0001t0008g0263others(1): Show | 4 | HG02717.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-12587A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946287 | ||||||
| chr4:70946430
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-12444G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946430 | ||||||
| chr4:70946447
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15-12427G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946447 | ||||||
| chr4:70946606
|
A | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-12268A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946606 | ||||||
| chr4:70946634
|
A | G | 1 | a0001c0001t0008g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15-12240A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946634 | ||||||
| chr4:70946641
|
A | G | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.15-12233A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946641 | ||||||
| chr4:70946714
|
T | C | 8 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-12160T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946714 | ||||||
| chr4:70946741
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.15-12133A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946741 | ||||||
| chr4:70946806
|
T | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-12068T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946806 | ||||||
| chr4:70946948
|
A | G | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-11926A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70946948 | ||||||
| chr4:70947021
|
A | G | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.15-11853A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947021 | ||||||
| chr4:70947048
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-11826C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947048 | ||||||
| chr4:70947088
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.15-11786G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947088 | ||||||
| chr4:70947124
|
G | T | 2 | a0001c0001t0005g0206a0001c0001t0005g0256 | 2 | NA18992.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.15-11750G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947124 | ||||||
| chr4:70947185
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.15-11689A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947185 | ||||||
| chr4:70947196
|
T | C | 1 | a0001c0001t0005g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.15-11678T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947196 | ||||||
| chr4:70947339
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.15-11535A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947339 | ||||||
| chr4:70947447
|
T | C | 66 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.15-11427T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947447 | ||||||
| chr4:70947455
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.15-11419G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947455 | ||||||
| chr4:70947476
|
T | A | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-11398T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947476 | ||||||
| chr4:70947577
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15-11297G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947577 | ||||||
| chr4:70947666
|
G | C | 4 | a0001c0001t0008g0070a0001c0001t0008g0262a0001c0001t0008g0263others(1): Show | 4 | HG02717.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-11208G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947666 | ||||||
| chr4:70947691
|
A | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-11183A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947691 | ||||||
| chr4:70947932
|
A | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0225 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.15-10942A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947932 | ||||||
| chr4:70947934
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-10940G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947934 | ||||||
| chr4:70947967
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.15-10907A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70947967 | ||||||
| chr4:70948342
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.15-10532C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70948342 | ||||||
| chr4:70948346
|
C | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-10528C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70948346 | ||||||
| chr4:70948394
|
G | A | 10 | a0001c0001t0004g0067a0001c0001t0004g0267a0001c0001t0004g0268others(7): Show | 10 | HG02615.hp2 HG02630.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-10480G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70948394 | ||||||
| chr4:70948571
|
GTC | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-10299_15-10298d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70948571 | |||||
| chr4:70948810
|
T | TAG | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.15-10061_15-10060d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70948810 | |||||
| chr4:70948979
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.15-9895C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70948979 | ||||||
| chr4:70949265
|
A | G | 1 | a0001c0001t0021g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.15-9609A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949265 | ||||||
| chr4:70949327
|
T | G | 9 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269others(6): Show | 9 | HG02615.hp2 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.15-9547T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949327 | ||||||
| chr4:70949427
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.15-9447C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949427 | ||||||
| chr4:70949486
|
A | T | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(44): Show | 47 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.15-9388A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949486 | ||||||
| chr4:70949556
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.15-9318G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949556 | ||||||
| chr4:70949581
|
T | G | 1 | a0001c0001t0008g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.15-9293T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949581 | ||||||
| chr4:70949585
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.15-9289G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949585 | ||||||
| chr4:70949719
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15-9155C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949719 | ||||||
| chr4:70949737
|
C | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-9137C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949737 | ||||||
| chr4:70949783
|
A | G | 1 | a0001c0001t0004g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.15-9091A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949783 | ||||||
| chr4:70949797
|
C | T | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.15-9077C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949797 | ||||||
| chr4:70949904
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0242 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.15-8970G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70949904 | ||||||
| chr4:70950160
|
G | C | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.15-8714G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950160 | ||||||
| chr4:70950252
|
A | G | 1 | a0001c0001t0006g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15-8622A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950252 | ||||||
| chr4:70950382
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.15-8492C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950382 | ||||||
| chr4:70950427
|
C | CA | 9 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0098others(6): Show | 9 | HG01109.hp2 HG01978.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.15-8425dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70950427 | |||||
| chr4:70950427
|
CA | C | 17 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0189others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.15-8425delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70950427 | |||||
| chr4:70950427
|
CAA | C | 101 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(98): Show | 101 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.15-8426_15-8425del others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70950427 | |||||
| chr4:70950749
|
C | T | 7 | a0001c0001t0006g0047a0001c0001t0006g0053a0001c0001t0006g0057others(4): Show | 7 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-8125C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950749 | ||||||
| chr4:70950760
|
T | G | 1 | a0001c0001t0004g0282 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15-8114T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950760 | ||||||
| chr4:70950761
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15-8113C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950761 | ||||||
| chr4:70950763
|
G | C | 1 | a0001c0001t0004g0282 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15-8111G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70950763 | ||||||
| chr4:70951159
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-7715G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951159 | ||||||
| chr4:70951253
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-7621C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951253 | ||||||
| chr4:70951425
|
G | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-7449G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951425 | ||||||
| chr4:70951598
|
T | C | 1 | a0001c0001t0026g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-7276T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951598 | ||||||
| chr4:70951635
|
A | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-7239A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951635 | ||||||
| chr4:70951674
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0144 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.15-7200G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951674 | ||||||
| chr4:70951676
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0036 | 3 | HG00673.hp2 HG02015.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.15-7198T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951676 | ||||||
| chr4:70951907
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0098 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.15-6967T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951907 | ||||||
| chr4:70951936
|
A | G | 1 | a0001c0001t0008g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.15-6938A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951936 | ||||||
| chr4:70951993
|
T | C | 85 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(82): Show | 85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.15-6881T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70951993 | ||||||
| chr4:70952110
|
C | T | 115 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(112): Show | 115 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.15-6764C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952110 | ||||||
| chr4:70952114
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.15-6760C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952114 | ||||||
| chr4:70952115
|
G | C | 3 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0002g0046 | 3 | NA18955.hp2 NA18975.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.15-6759G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952115 | ||||||
| chr4:70952263
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15-6611A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952263 | ||||||
| chr4:70952416
|
G | C | 14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.15-6458G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952416 | ||||||
| chr4:70952512
|
G | A | 48 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(45): Show | 48 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.15-6362G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952512 | ||||||
| chr4:70952642
|
C | CA | 84 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0105others(81): Show | 84 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.15-6215dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70952642 | |||||
| chr4:70952642
|
C | CAA | 10 | a0001c0001t0001g0239a0001c0001t0002g0023a0001c0001t0002g0031others(7): Show | 10 | HG02074.hp1 HG02602.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.15-6216_15-6215dup others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70952642 | |||||
| chr4:70952642
|
CA | C | 8 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-6215delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70952642 | |||||
| chr4:70952653
|
A | C | 1 | a0001c0001t0019g0283 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15-6221A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952653 | ||||||
| chr4:70952655
|
A | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-6219A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952655 | ||||||
| chr4:70952676
|
A | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-6198A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952676 | ||||||
| chr4:70952804
|
A | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-6070A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952804 | ||||||
| chr4:70952873
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-6001T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952873 | ||||||
| chr4:70952883
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.15-5991C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952883 | ||||||
| chr4:70952935
|
C | CT | 38 | a0001c0001t0001g0068a0001c0001t0001g0101a0001c0001t0001g0105others(35): Show | 38 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.15-5914dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70952935 | |||||
| chr4:70952935
|
CT | C | 49 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(46): Show | 49 | HG00408.hp2 HG00673.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.15-5914delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70952935 | |||||
| chr4:70952935
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-5922_15-5914del others(9): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70952935 | |||||
| chr4:70952957
|
T | C | 28 | a0001c0001t0003g0075a0001c0001t0003g0082a0001c0001t0003g0085others(25): Show | 28 | HG00673.hp1 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.15-5917T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70952957 | ||||||
| chr4:70953016
|
C | T | 2 | a0001c0001t0007g0275a0001c0001t0007g0277 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.15-5858C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953016 | ||||||
| chr4:70953096
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.15-5778G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953096 | ||||||
| chr4:70953150
|
G | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-5724G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953150 | ||||||
| chr4:70953177
|
G | T | 3 | a0001c0001t0008g0010a0001c0001t0008g0084a0001c0001t0008g0224 | 3 | HG01167.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.15-5697G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953177 | ||||||
| chr4:70953185
|
C | T | 17 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.15-5689C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953185 | ||||||
| chr4:70953297
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.15-5577G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953297 | ||||||
| chr4:70953316
|
G | C | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-5558G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953316 | ||||||
| chr4:70953552
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.15-5322T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953552 | ||||||
| chr4:70953693
|
C | T | 2 | a0001c0001t0006g0057a0001c0001t0006g0059 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.15-5181C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953693 | ||||||
| chr4:70953850
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.15-5024A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70953850 | ||||||
| chr4:70954051
|
G | A | 116 | a0001c0001t0001g0062a0001c0001t0002g0004a0001c0001t0002g0005others(113): Show | 116 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.15-4823G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70954051 | ||||||
| chr4:70954322
|
A | AT | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-4547dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70954322 | |||||
| chr4:70954463
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-4411C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70954463 | ||||||
| chr4:70954782
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0195 | 2 | HG02451.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.15-4092G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70954782 | ||||||
| chr4:70954800
|
G | C | 1 | a0001c0001t0002g0036 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.15-4074G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70954800 | ||||||
| chr4:70955081
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.15-3793C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955081 | ||||||
| chr4:70955167
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-3707G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955167 | ||||||
| chr4:70955405
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.15-3469A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955405 | ||||||
| chr4:70955408
|
C | G | 3 | a0001c0001t0008g0262a0001c0001t0008g0263a0001c0001t0008g0264 | 3 | HG02717.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.15-3466C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955408 | ||||||
| chr4:70955410
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(55): Show | 58 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.15-3464C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955410 | ||||||
| chr4:70955457
|
A | G | 4 | a0001c0001t0008g0070a0001c0001t0008g0262a0001c0001t0008g0263others(1): Show | 4 | HG02717.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-3417A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955457 | ||||||
| chr4:70955464
|
C | CT | 123 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0071others(120): Show | 123 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.15-3388dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70955464 | |||||
| chr4:70955464
|
C | CTT | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0136others(6): Show | 9 | HG00621.hp1 HG01167.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.15-3389_15-3388dup others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70955464 | |||||
| chr4:70955762
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0239a0001c0001t0001g0241others(1): Show | 4 | HG02922.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-3112C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70955762 | ||||||
| chr4:70956051
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.15-2823A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956051 | ||||||
| chr4:70956163
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15-2711G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956163 | ||||||
| chr4:70956320
|
G | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-2554G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956320 | ||||||
| chr4:70956326
|
C | G | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-2548C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956326 | ||||||
| chr4:70956517
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-2357A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956517 | ||||||
| chr4:70956641
|
T | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-2233T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956641 | ||||||
| chr4:70956970
|
G | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-1904G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70956970 | ||||||
| chr4:70957100
|
G | GT | 64 | a0001c0001t0001g0062a0001c0001t0001g0136a0001c0001t0001g0165others(61): Show | 64 | HG00438.hp1 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.15-1758dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957100 | |||||
| chr4:70957105
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.15-1769T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957105 | ||||||
| chr4:70957188
|
A | T | 21 | a0001c0001t0001g0077a0001c0001t0001g0117a0001c0001t0001g0121others(18): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-1686A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957188 | ||||||
| chr4:70957247
|
G | A | 2 | a0001c0001t0006g0050a0001c0001t0006g0051 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.15-1627G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957247 | ||||||
| chr4:70957259
|
C | CA | 53 | a0001c0001t0001g0109a0001c0001t0001g0119a0001c0001t0001g0147others(50): Show | 53 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.15-1596dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957259 | |||||
| chr4:70957259
|
CA | C | 60 | a0001c0001t0001g0196a0001c0001t0002g0005a0001c0001t0002g0007others(57): Show | 60 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.15-1596delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957259 | |||||
| chr4:70957259
|
CAAA | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-1598_15-1596del others(3): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957259 | |||||
| chr4:70957423
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.15-1451G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957423 | ||||||
| chr4:70957434
|
C | CT | 24 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0105others(21): Show | 24 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.15-1425dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957434 | |||||
| chr4:70957436
|
T | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.15-1438T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957436 | ||||||
| chr4:70957475
|
C | T | 3 | a0001c0001t0005g0103a0001c0001t0005g0201a0001c0001t0005g0208 | 3 | HG00642.hp1 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.15-1399C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957475 | ||||||
| chr4:70957508
|
A | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-1366A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957508 | ||||||
| chr4:70957522
|
C | T | 1 | a0001c0001t0005g0209 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15-1352C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957522 | ||||||
| chr4:70957555
|
C | T | 17 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.15-1319C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957555 | ||||||
| chr4:70957645
|
A | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.15-1229A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957645 | ||||||
| chr4:70957666
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-1208C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957666 | ||||||
| chr4:70957703
|
C | G | 1 | a0001c0001t0002g0026 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.15-1171C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957703 | ||||||
| chr4:70957711
|
T | A | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.15-1163T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957711 | ||||||
| chr4:70957753
|
A | AT | 6 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0009g0177others(3): Show | 6 | HG00408.hp1 HG02074.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-1103dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957753 | |||||
| chr4:70957753
|
AT | A | 107 | a0001c0001t0001g0125a0001c0001t0001g0149a0001c0001t0001g0196others(104): Show | 107 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.15-1103delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957753 | |||||
| chr4:70957753
|
ATT | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0048a0001c0001t0004g0282others(4): Show | 7 | HG01891.hp2 HG01975.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-1104_15-1103del others(2): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70957753 | |||||
| chr4:70957756
|
T | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0239a0001c0001t0001g0241others(1): Show | 4 | HG02922.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-1118T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957756 | ||||||
| chr4:70957757
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15-1117T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957757 | ||||||
| chr4:70957758
|
T | A | 8 | a0001c0001t0003g0075a0001c0001t0007g0275a0001c0001t0007g0276others(5): Show | 8 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-1116T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957758 | ||||||
| chr4:70957798
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-1076C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957798 | ||||||
| chr4:70957986
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15-888A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70957986 | ||||||
| chr4:70958009
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0163 | 2 | NA18942.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.15-865G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958009 | ||||||
| chr4:70958013
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.15-861C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958013 | ||||||
| chr4:70958024
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.15-850T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958024 | ||||||
| chr4:70958065
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.15-809C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958065 | ||||||
| chr4:70958168
|
CT | C | 12 | a0001c0001t0001g0077a0001c0001t0001g0195a0001c0001t0001g0212others(9): Show | 12 | HG01168.hp1 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.15-692delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70958168 | |||||
| chr4:70958187
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-687C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958187 | ||||||
| chr4:70958204
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.15-670G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958204 | ||||||
| chr4:70958251
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.15-623G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958251 | ||||||
| chr4:70958284
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15-590C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958284 | ||||||
| chr4:70958363
|
C | T | 2 | a0001c0001t0003g0221a0001c0001t0003g0222 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.15-511C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958363 | ||||||
| chr4:70958396
|
AC | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-475delC | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 70958396 | |||||
| chr4:70958602
|
C | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-272C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958602 | ||||||
| chr4:70958702
|
C | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA19005.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.15-172C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958702 | ||||||
| chr4:70958820
|
A | G | 42 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.15-54A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70958820 | ||||||
| chr4:70959071
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+31G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959071 | ||||||
| chr4:70959084
|
A | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0143 | 2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.181+44A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959084 | ||||||
| chr4:70959313
|
G | A | 217 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0071others(214): Show | 217 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.181+273G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959313 | ||||||
| chr4:70959454
|
T | C | 1 | a0001c0001t0025g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.181+414T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959454 | ||||||
| chr4:70959629
|
G | A | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.181+589G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959629 | ||||||
| chr4:70959754
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+714T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959754 | ||||||
| chr4:70959772
|
A | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+732A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959772 | ||||||
| chr4:70959823
|
A | G | 30 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(27): Show | 30 | HG00673.hp1 HG01123.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.181+783A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959823 | ||||||
| chr4:70959878
|
TTTTTTA | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+855_181+860del others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70959878 | |||||
| chr4:70959924
|
C | G | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.181+884C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70959924 | ||||||
| chr4:70960037
|
C | G | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.181+997C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960037 | ||||||
| chr4:70960157
|
C | A | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181+1117C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960157 | ||||||
| chr4:70960199
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.181+1159A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960199 | ||||||
| chr4:70960243
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.181+1203A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960243 | ||||||
| chr4:70960342
|
C | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+1302C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960342 | ||||||
| chr4:70960466
|
A | G | 1 | a0001c0001t0008g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181+1426A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960466 | ||||||
| chr4:70960530
|
T | C | 1 | a0001c0001t0002g0017 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.181+1490T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960530 | ||||||
| chr4:70960580
|
G | A | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.181+1540G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960580 | ||||||
| chr4:70960643
|
T | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.181+1603T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960643 | ||||||
| chr4:70960676
|
G | C | 1 | a0001c0001t0008g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.181+1636G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70960676 | ||||||
| chr4:70961019
|
T | C | 2 | a0001c0001t0003g0076a0001c0001t0003g0089 | 2 | NA18995.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.181+1979T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70961019 | ||||||
| chr4:70961028
|
C | T | 2 | a0001c0001t0003g0076a0001c0001t0003g0089 | 2 | NA18995.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.181+1988C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70961028 | ||||||
| chr4:70961048
|
C | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+2008C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70961048 | ||||||
| chr4:70961327
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.181+2287C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70961327 | ||||||
| chr4:70961458
|
C | G | 2 | a0001c0001t0001g0260a0001c0001t0020g0261 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.181+2418C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70961458 | ||||||
| chr4:70961551
|
C | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.181+2511C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70961551 | ||||||
| chr4:70962282
|
A | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.181+3242A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70962282 | ||||||
| chr4:70962376
|
A | T | 2 | a0001c0001t0005g0202a0001c0001t0005g0207 | 2 | HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.181+3336A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70962376 | ||||||
| chr4:70962619
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+3579G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70962619 | ||||||
| chr4:70962675
|
A | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0128a0001c0001t0001g0130others(2): Show | 5 | HG00609.hp2 HG02027.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+3635A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70962675 | ||||||
| chr4:70962766
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+3726C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70962766 | ||||||
| chr4:70962990
|
C | T | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+3950C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70962990 | ||||||
| chr4:70963427
|
GATAA | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0168a0001c0001t0001g0244 | 3 | NA18948.hp1 NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.181+4391_181+4394d others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70963427 | |||||
| chr4:70963577
|
T | C | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.181+4537T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70963577 | ||||||
| chr4:70963692
|
C | T | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.181+4652C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70963692 | ||||||
| chr4:70963697
|
G | C | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.181+4657G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70963697 | ||||||
| chr4:70963827
|
GA | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+4794delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70963827 | |||||
| chr4:70963851
|
CCAAA | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+4818_181+4821d others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70963851 | |||||
| chr4:70963923
|
A | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+4883A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70963923 | ||||||
| chr4:70964130
|
T | G | 2 | a0001c0001t0006g0050a0001c0001t0006g0051 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.181+5090T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70964130 | ||||||
| chr4:70964223
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.181+5183A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70964223 | ||||||
| chr4:70964651
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.182-5280C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70964651 | ||||||
| chr4:70964761
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.182-5170C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70964761 | ||||||
| chr4:70964791
|
G | A | 4 | a0001c0001t0008g0070a0001c0001t0008g0262a0001c0001t0008g0263others(1): Show | 4 | HG02717.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-5140G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70964791 | ||||||
| chr4:70964869
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-5062G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70964869 | ||||||
| chr4:70965024
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.182-4907G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965024 | ||||||
| chr4:70965208
|
A | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.182-4723A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965208 | ||||||
| chr4:70965296
|
C | CA | 94 | a0001c0001t0001g0184a0001c0001t0001g0193a0001c0001t0001g0199others(91): Show | 94 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.182-4611dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965296 | |||||
| chr4:70965296
|
C | CAA | 16 | a0001c0001t0002g0004a0001c0001t0002g0040a0001c0001t0002g0044others(13): Show | 16 | HG01243.hp2 HG02258.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-4612_182-4611d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965296 | |||||
| chr4:70965296
|
CA | C | 14 | a0001c0001t0001g0066a0001c0001t0001g0110a0001c0001t0001g0113others(11): Show | 14 | HG00597.hp1 HG01070.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.182-4611delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965296 | |||||
| chr4:70965296
|
CAAAA | C | 6 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0278others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-4614_182-4611d others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965296 | |||||
| chr4:70965598
|
G | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-4333G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965598 | ||||||
| chr4:70965614
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG00597.hp1 HG02074.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-4317G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965614 | ||||||
| chr4:70965721
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.182-4210C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965721 | ||||||
| chr4:70965733
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-4198T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965733 | ||||||
| chr4:70965741
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-4190G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965741 | ||||||
| chr4:70965741
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.182-4190G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965741 | ||||||
| chr4:70965776
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.182-4155G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965776 | ||||||
| chr4:70965784
|
G | A | 1 | a0001c0001t0011g0265 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.182-4147G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965784 | ||||||
| chr4:70965796
|
C | CA | 65 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0068others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.182-4107dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965796
|
C | CAA | 15 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0001g0128others(12): Show | 15 | HG00741.hp2 HG01167.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-4108_182-4107d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965796
|
C | CAAA | 7 | a0001c0001t0004g0069a0001c0001t0004g0080a0001c0001t0004g0081others(4): Show | 7 | HG00323.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-4109_182-4107d others(5): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965796
|
C | CAAAAA | 12 | a0001c0001t0003g0082a0001c0001t0003g0088a0001c0001t0003g0089others(9): Show | 12 | HG00673.hp1 HG02129.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.182-4111_182-4107d others(7): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965796
|
CA | C | 27 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(24): Show | 27 | HG00438.hp2 HG00673.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.182-4107delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965796
|
CAA | C | 45 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG01975.hp1 others(42): Show |
intron_variant | MODIFIER | c.182-4108_182-4107d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965796
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.182-4118_182-4107d others(14): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70965796 | |||||
| chr4:70965972
|
C | T | 117 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(114): Show | 117 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.182-3959C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965972 | ||||||
| chr4:70965979
|
C | G | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-3952C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70965979 | ||||||
| chr4:70966043
|
G | C | 1 | a0001c0001t0015g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.182-3888G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966043 | ||||||
| chr4:70966228
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.182-3703T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966228 | ||||||
| chr4:70966374
|
C | CT | 15 | a0001c0001t0001g0152a0001c0001t0001g0199a0001c0001t0002g0043others(12): Show | 15 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.182-3540dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70966374 | |||||
| chr4:70966500
|
G | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-3431G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966500 | ||||||
| chr4:70966620
|
T | C | 1 | a0001c0001t0005g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.182-3311T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966620 | ||||||
| chr4:70966749
|
G | C | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(55): Show | 58 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.182-3182G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966749 | ||||||
| chr4:70966845
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-3086T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966845 | ||||||
| chr4:70966847
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.182-3084C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966847 | ||||||
| chr4:70966858
|
AT | A | 14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.182-3072delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70966858 | ||||||
| chr4:70966866
|
GA | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-3057delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70966866 | |||||
| chr4:70967019
|
T | C | 65 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0077others(62): Show | 65 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.182-2912T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70967019 | ||||||
| chr4:70967157
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0194 | 2 | HG00738.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.182-2774G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70967157 | ||||||
| chr4:70967307
|
G | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.182-2624G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70967307 | ||||||
| chr4:70967441
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.182-2490G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70967441 | ||||||
| chr4:70967459
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.182-2472G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70967459 | ||||||
| chr4:70967726
|
G | GA | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.182-2197dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 70967726 | |||||
| chr4:70967730
|
A | G | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-2201A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70967730 | ||||||
| chr4:70968045
|
C | T | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.182-1886C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968045 | ||||||
| chr4:70968095
|
A | G | 1 | a0001c0001t0026g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.182-1836A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968095 | ||||||
| chr4:70968145
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-1786C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968145 | ||||||
| chr4:70968164
|
G | A | 10 | a0001c0001t0004g0067a0001c0001t0004g0267a0001c0001t0004g0268others(7): Show | 10 | HG02615.hp2 HG02630.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.182-1767G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968164 | ||||||
| chr4:70968287
|
A | T | 1 | a0001c0001t0024g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.182-1644A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968287 | ||||||
| chr4:70968353
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.182-1578C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968353 | ||||||
| chr4:70968374
|
C | T | 1 | a0001c0001t0019g0283 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.182-1557C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968374 | ||||||
| chr4:70968600
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0098 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.182-1331C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968600 | ||||||
| chr4:70968751
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.182-1180C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968751 | ||||||
| chr4:70968823
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182-1108A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968823 | ||||||
| chr4:70968831
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.182-1100C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968831 | ||||||
| chr4:70968881
|
C | G | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.182-1050C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70968881 | ||||||
| chr4:70969170
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.182-761C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70969170 | ||||||
| chr4:70969759
|
G | C | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.182-172G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 2/5 | chr4 | 70969759 | ||||||
| chr4:70970105
|
G | A | 112 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(109): Show | 112 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.275+81G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70970105 | ||||||
| chr4:70970338
|
C | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0136a0001c0001t0001g0238 | 3 | HG01167.hp2 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.275+314C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70970338 | ||||||
| chr4:70970388
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+364C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70970388 | ||||||
| chr4:70970390
|
A | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+366A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70970390 | ||||||
| chr4:70970888
|
C | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+864C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70970888 | ||||||
| chr4:70971122
|
T | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1098T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971122 | ||||||
| chr4:70971129
|
C | T | 2 | a0001c0001t0007g0276a0001c0001t0007g0279 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.275+1105C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971129 | ||||||
| chr4:70971142
|
A | C | 17 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.275+1118A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971142 | ||||||
| chr4:70971296
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.275+1272G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971296 | ||||||
| chr4:70971366
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275+1342G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971366 | ||||||
| chr4:70971455
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275+1431C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971455 | ||||||
| chr4:70971478
|
C | G | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.275+1454C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971478 | ||||||
| chr4:70971504
|
C | CA | 8 | a0001c0001t0001g0140a0001c0001t0001g0165a0001c0001t0001g0170others(5): Show | 8 | HG01975.hp2 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+1498dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70971504 | |||||
| chr4:70971504
|
CA | C | 12 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0196others(9): Show | 12 | HG01168.hp2 HG01943.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.275+1498delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70971504 | |||||
| chr4:70971623
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.275+1599C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971623 | ||||||
| chr4:70971762
|
A | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0195others(1): Show | 4 | HG02451.hp2 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.275+1738A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971762 | ||||||
| chr4:70971933
|
CCTT | C | 55 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.275+1913_275+1915d others(5): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70971933 | |||||
| chr4:70971936
|
T | C | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.275+1912T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70971936 | ||||||
| chr4:70972007
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0068others(72): Show | 76 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.275+1983C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972007 | ||||||
| chr4:70972008
|
C | CT | 10 | a0001c0001t0002g0004a0001c0001t0004g0273a0001c0001t0008g0010others(7): Show | 10 | HG01167.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.275+1995dupT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70972008 | |||||
| chr4:70972020
|
G | T | 112 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(109): Show | 112 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.275+1996G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972020 | ||||||
| chr4:70972072
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0163 | 2 | NA18942.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.275+2048G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972072 | ||||||
| chr4:70972275
|
G | A | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.275+2251G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972275 | ||||||
| chr4:70972365
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.275+2341C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972365 | ||||||
| chr4:70972574
|
C | G | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+2550C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972574 | ||||||
| chr4:70972699
|
T | C | 112 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(109): Show | 112 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.276-2454T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972699 | ||||||
| chr4:70972758
|
ATTATT | A | 112 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(109): Show | 112 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.276-2367_276-2363d others(7): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70972758 | |||||
| chr4:70972821
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-2332C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972821 | ||||||
| chr4:70972837
|
G | C | 30 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(27): Show | 30 | HG00673.hp1 HG01123.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.276-2316G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972837 | ||||||
| chr4:70972926
|
A | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-2227A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972926 | ||||||
| chr4:70972934
|
C | T | 15 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(12): Show | 15 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.276-2219C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972934 | ||||||
| chr4:70972935
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.276-2218G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972935 | ||||||
| chr4:70972989
|
T | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-2164T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972989 | ||||||
| chr4:70972994
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-2159T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972994 | ||||||
| chr4:70972995
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-2158G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70972995 | ||||||
| chr4:70973002
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-2151T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973002 | ||||||
| chr4:70973008
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-2145C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973008 | ||||||
| chr4:70973009
|
A | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(2): Show | 5 | HG02922.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-2144A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973009 | ||||||
| chr4:70973016
|
G | A | 7 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0239others(4): Show | 7 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-2137G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973016 | ||||||
| chr4:70973024
|
C | T | 9 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.276-2129C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973024 | ||||||
| chr4:70973025
|
G | A | 14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.276-2128G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973025 | ||||||
| chr4:70973033
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.276-2120A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973033 | ||||||
| chr4:70973064
|
C | T | 4 | a0001c0001t0005g0103a0001c0001t0005g0201a0001c0001t0005g0208others(1): Show | 4 | HG00642.hp1 HG01071.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-2089C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973064 | ||||||
| chr4:70973124
|
A | T | 1 | a0001c0001t0027g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.276-2029A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973124 | ||||||
| chr4:70973185
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0195 | 2 | HG02451.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.276-1968A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973185 | ||||||
| chr4:70973246
|
G | A | 2 | a0001c0001t0006g0053a0001c0001t0006g0061 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.276-1907G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973246 | ||||||
| chr4:70973381
|
G | A | 1 | a0001c0001t0016g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.276-1772G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973381 | ||||||
| chr4:70973390
|
C | T | 1 | a0001c0001t0004g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.276-1763C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973390 | ||||||
| chr4:70973469
|
C | CA | 32 | a0001c0001t0001g0066a0001c0001t0001g0108a0001c0001t0001g0111others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.276-1660dupA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70973469 | |||||
| chr4:70973469
|
CA | C | 41 | a0001c0001t0001g0134a0001c0001t0001g0153a0001c0001t0001g0196others(38): Show | 41 | HG00323.hp1 HG00673.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.276-1660delA | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70973469 | |||||
| chr4:70973469
|
CAA | C | 12 | a0001c0001t0003g0085a0001c0001t0003g0090a0001c0001t0003g0221others(9): Show | 12 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.276-1661_276-1660d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 70973469 | |||||
| chr4:70973483
|
A | C | 2 | a0001c0001t0003g0085a0001c0001t0003g0225 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.276-1670A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973483 | ||||||
| chr4:70973543
|
G | A | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(44): Show | 47 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.276-1610G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973543 | ||||||
| chr4:70973791
|
GT | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-1361delT | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973791 | ||||||
| chr4:70973835
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.276-1318G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973835 | ||||||
| chr4:70973838
|
C | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0056 | 2 | HG00438.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.276-1315C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973838 | ||||||
| chr4:70973910
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.276-1243A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973910 | ||||||
| chr4:70973921
|
A | G | 2 | a0001c0001t0005g0206a0001c0001t0005g0256 | 2 | NA18992.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.276-1232A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973921 | ||||||
| chr4:70973930
|
C | G | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(44): Show | 47 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.276-1223C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70973930 | ||||||
| chr4:70974138
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.276-1015G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974138 | ||||||
| chr4:70974191
|
C | T | 47 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(44): Show | 47 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.276-962C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974191 | ||||||
| chr4:70974256
|
G | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-897G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974256 | ||||||
| chr4:70974313
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.276-840A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974313 | ||||||
| chr4:70974399
|
C | T | 2 | a0001c0001t0004g0273a0001c0001t0004g0282 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.276-754C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974399 | ||||||
| chr4:70974489
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.276-664G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974489 | ||||||
| chr4:70974579
|
C | T | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-574C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974579 | ||||||
| chr4:70974743
|
T | G | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.276-410T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974743 | ||||||
| chr4:70974757
|
A | G | 13 | a0001c0001t0006g0047a0001c0001t0006g0049a0001c0001t0006g0050others(10): Show | 13 | HG01243.hp1 HG02602.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.276-396A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974757 | ||||||
| chr4:70974975
|
T | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0027a0001c0001t0002g0030 | 3 | NA18948.hp2 NA18971.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.276-178T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70974975 | ||||||
| chr4:70975023
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.276-130A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 3/5 | chr4 | 70975023 | ||||||
| chr4:70975311
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.409+25A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70975311 | ||||||
| chr4:70975570
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.409+284C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70975570 | ||||||
| chr4:70976121
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.409+835C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976121 | ||||||
| chr4:70976286
|
G | C | 1 | a0001c0001t0008g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.409+1000G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976286 | ||||||
| chr4:70976721
|
T | A | 1 | a0001c0001t0003g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.409+1435T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976721 | ||||||
| chr4:70976753
|
C | CAT | 25 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0111others(22): Show | 25 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.409+1488_409+1489d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATAT | 3 | a0001c0001t0005g0103a0001c0001t0005g0207a0001c0001t0008g0224 | 3 | HG01167.hp1 HG03098.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.409+1486_409+1489d others(6): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(15): Show |
1 | a0001c0001t0011g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.409+1474_409+1475i others(24): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(17): Show |
1 | a0001c0001t0011g0265 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.409+1474_409+1475i others(26): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(3): Show |
1 | a0001c0001t0006g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.409+1480_409+1489d others(12): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(5): Show |
2 | a0001c0001t0006g0051a0001c0002t0006g0052 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.409+1478_409+1489d others(14): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(9): Show |
4 | a0001c0001t0002g0009a0001c0001t0006g0049a0001c0001t0026g0011others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1474_409+1489d others(18): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(11): Show |
1 | a0001c0001t0018g0002 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.409+1472_409+1489d others(20): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(13): Show |
1 | a0001c0001t0006g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.409+1470_409+1489d others(22): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(17): Show |
1 | a0001c0001t0006g0058 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.409+1489_409+1490i others(26): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(19): Show |
7 | a0001c0001t0006g0047a0001c0001t0006g0053a0001c0001t0006g0057others(4): Show | 7 | HG02602.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.409+1489_409+1490i others(28): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
C | CATATATA others(21): Show |
1 | a0001c0001t0023g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.409+1489_409+1490i others(30): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976753
|
CAT | C | 14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0082others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.409+1488_409+1489d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976753 | |||||
| chr4:70976758
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0007g0276a0001c0001t0007g0279a0001c0001t0007g0280 | 3 | HG02559.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.409+1489_409+1490i others(20): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976758 | |||||
| chr4:70976758
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0007g0275a0001c0001t0007g0277a0001c0001t0007g0278others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1487_409+1488i others(18): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976758 | |||||
| chr4:70976774
|
A | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0179a0001c0001t0001g0199 | 3 | HG01433.hp2 HG02735.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.409+1488A>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976774 | ||||||
| chr4:70976774
|
ATC | A | 7 | a0001c0001t0001g0260a0001c0001t0003g0085a0001c0001t0003g0086others(4): Show | 7 | HG02451.hp1 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.409+1499_409+1500d others(4): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976774 | |||||
| chr4:70976774
|
ATCTCTC | A | 40 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(37): Show | 40 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.409+1495_409+1500d others(8): Show |
MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 70976774 | |||||
| chr4:70976776
|
C | A | 138 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0073others(135): Show | 138 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.409+1490C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976776 | ||||||
| chr4:70976778
|
C | A | 156 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0074others(153): Show | 156 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.409+1492C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976778 | ||||||
| chr4:70976780
|
C | A | 46 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0027others(43): Show | 46 | HG00323.hp1 HG00735.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.409+1494C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976780 | ||||||
| chr4:70976782
|
C | A | 115 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(112): Show | 115 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.409+1496C>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976782 | ||||||
| chr4:70976918
|
A | G | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.409+1632A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976918 | ||||||
| chr4:70976982
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.409+1696C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976982 | ||||||
| chr4:70976989
|
C | G | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.409+1703C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70976989 | ||||||
| chr4:70977004
|
A | G | 1 | a0001c0001t0008g0224 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.409+1718A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977004 | ||||||
| chr4:70977050
|
G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | NA18962.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.409+1764G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977050 | ||||||
| chr4:70977151
|
C | T | 115 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(112): Show | 115 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.409+1865C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977151 | ||||||
| chr4:70977167
|
G | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.409+1881G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977167 | ||||||
| chr4:70977193
|
C | G | 2 | a0001c0001t0005g0206a0001c0001t0005g0256 | 2 | NA18992.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.409+1907C>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977193 | ||||||
| chr4:70977225
|
T | C | 4 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0081others(1): Show | 4 | HG00323.hp1 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-1903T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977225 | ||||||
| chr4:70977411
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.410-1717C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977411 | ||||||
| chr4:70977521
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0234 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.410-1607A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977521 | ||||||
| chr4:70977530
|
G | T | 1 | a0001c0001t0002g0043 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.410-1598G>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977530 | ||||||
| chr4:70977698
|
A | T | 14 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0004g0079others(11): Show | 14 | HG00735.hp2 HG01515.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.410-1430A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977698 | ||||||
| chr4:70977802
|
C | T | 1 | a0001c0001t0022g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.410-1326C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977802 | ||||||
| chr4:70977822
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410-1306C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70977822 | ||||||
| chr4:70978032
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.410-1096C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70978032 | ||||||
| chr4:70978230
|
G | C | 2 | a0001c0001t0018g0002a0001c0001t0023g0003 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.410-898G>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70978230 | ||||||
| chr4:70978401
|
G | A | 113 | a0001c0001t0001g0113a0001c0001t0002g0004a0001c0001t0002g0005others(110): Show | 113 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.410-727G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70978401 | ||||||
| chr4:70978571
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.410-557C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70978571 | ||||||
| chr4:70979096
|
T | C | 2 | a0001c0001t0002g0009a0001c0001t0026g0011 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.410-32T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 4/5 | chr4 | 70979096 | ||||||
| chr4:70979842
|
T | G | 5 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0044others(2): Show | 5 | NA18942.hp2 NA18955.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+551T>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70979842 | ||||||
| chr4:70979934
|
T | C | 2 | a0001c0001t0005g0206a0001c0001t0005g0256 | 2 | NA18992.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.573+643T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70979934 | ||||||
| chr4:70980207
|
T | C | 1 | a0001c0001t0017g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.573+916T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70980207 | ||||||
| chr4:70980613
|
T | C | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+1322T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70980613 | ||||||
| chr4:70980614
|
G | A | 7 | a0001c0001t0007g0275a0001c0001t0007g0276a0001c0001t0007g0277others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+1323G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70980614 | ||||||
| chr4:70980810
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.574-1170A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70980810 | ||||||
| chr4:70981059
|
A | T | 1 | a0001c0001t0004g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.574-921A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981059 | ||||||
| chr4:70981158
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.574-822G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981158 | ||||||
| chr4:70981219
|
T | C | 8 | a0001c0001t0008g0010a0001c0001t0008g0070a0001c0001t0008g0084others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-761T>C | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981219 | ||||||
| chr4:70981353
|
T | A | 2 | a0001c0001t0002g0009a0001c0001t0026g0011 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.574-627T>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981353 | ||||||
| chr4:70981486
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.574-494A>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981486 | ||||||
| chr4:70981507
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.574-473C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981507 | ||||||
| chr4:70981564
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0014others(8): Show | 11 | HG00408.hp2 HG00438.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-416A>G | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981564 | ||||||
| chr4:70981569
|
G | A | 45 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.574-411G>A | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 5/5 | chr4 | 70981569 |