Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 216 | 283 | 86 | 46 | 111 | 8 | 30 | 79 | MOB1B_chr4_70897369_70993168 | MOB1B | MSFLF others(211): Show |
chr4 | 70897369 | 70993168 |
| a0002 | 0/0 | 216 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | MSFLF others(211): Show |
chr4 | 70897369 | 70993168 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 648 | 282 | 86 | 45 | 111 | 8 | 30 | MOB1B_chr4_70897369_70993168 | MOB1B | ATGAG others(643): Show |
chr4 | 70897369 | 70993168 | ||
| a0001c0002 | 0/0 | 648 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATGAG others(643): Show |
chr4 | 70897369 | 70993168 | ||
| a0002c0003 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATGAG others(643): Show |
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 | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0002 | 0/0 | 6930 | 41 | 3 | 2 | 34 | 0 | 2 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0003 | 1/0 | 6930 | 21 | 6 | 1 | 9 | 0 | 4 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0004 | 0/0 | 6930 | 15 | 11 | 1 | 0 | 3 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0005 | 0/0 | 6930 | 13 | 1 | 2 | 5 | 0 | 5 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0006 | 0/0 | 6930 | 11 | 10 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0007 | 0/0 | 6930 | 7 | 7 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0008 | 0/0 | 6930 | 7 | 6 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0009 | 0/0 | 6930 | 5 | 0 | 0 | 5 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0010 | 0/0 | 6930 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0011 | 0/0 | 6930 | 2 | 2 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0012 | 0/0 | 6930 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0013 | 0/0 | 6930 | 2 | 0 | 0 | 2 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0014 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0015 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0016 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0017 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0018 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0019 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0020 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0021 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0022 | 0/0 | 6930 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0023 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0024 | 0/0 | 6930 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0025 | 0/0 | 6930 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0026 | 0/0 | 6930 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0001t0027 | 0/0 | 6930 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0001c0002t0006 | 0/0 | 6930 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
chr4 | 70897369 | 70993168 |
| a0002c0003t0001 | 0/0 | 6930 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | ATTGG others(6925): Show |
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 |
| a0001c0001t0001g0072 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0122 | 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 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0070 | 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 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0005g0211 | 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 |
| a0001c0001t0008g0071 | 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 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0009g0182 | 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 |
| a0001c0001t0012g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0013g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0013g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0014g0204 | 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 |
| a0001c0001t0021g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| a0001c0001t0022g0201 | 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 |
| a0002c0003t0001g0181 | 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 | g0189 | EUR | GBR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0217 | 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 | g0216 | EUR | FIN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0178 | 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 | g0155 | 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 | g0175 | 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 | g0210 | 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 | g0202 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0215 | 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 | g0032 | 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 | g0195 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0187 | 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 | g0163 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0209 | 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 | g0137 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0197 | 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 | g0214 | 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 | g0147 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01261 | hp1 | a0001 | c0001 | t0022 | g0201 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0106 | 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 | g0105 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0140 | 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 | g0139 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | 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 | g0165 | 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 | g0107 | 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 | g0129 | 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 | g0183 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0136 | 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 | g0131 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | 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 | g0160 | 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 | g0120 | 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 | g0158 | 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 | g0191 | 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 | g0196 | 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 | g0103 | 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 | g0049 | 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 | g0180 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0143 | 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 | g0132 | 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 | g0138 | AFR | GWD | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0149 | 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 | g0190 | 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 | g0051 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0150 | 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 | g0161 | SAS | PJL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0205 | 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 | g0168 | 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 | g0104 | 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 | g0270 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0060 | 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 | g0269 | AFR | ESN | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0146 | 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 | g0027 | 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 | g0130 | AFR | MSL | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0050 | 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 | g0208 | 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 | g0059 | 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 | g0185 | 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 | g0204 | 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 | g0118 | SAS | BEB | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0203 | 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 | g0100 | SAS | STU | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0156 | 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 | g0128 | AFR | YRI | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0110 | 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 | g0164 | 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 | g0177 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0102 | 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 | g0109 | 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 | g0206 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18956 | hp2 | a0001 | c0001 | t0013 | g0123 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0159 | 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 | g0154 | 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 | g0169 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0026 | 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 | g0182 | 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 | g0117 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0028 | 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 | g0111 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA18983 | hp1 | a0001 | c0001 | t0012 | g0176 | 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 | g0207 | 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 | g0184 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0179 | 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 | g0192 | 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 | g0194 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0148 | 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 | g0071 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19057 | hp1 | a0001 | c0001 | t0013 | g0212 | 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 | g0101 | 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 | g0116 | 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 | g0072 | 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 | g0114 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19082 | hp2 | a0002 | c0003 | t0001 | g0181 | 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 | g0211 | EAS | JPT | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0151 | 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 | g0198 | AFR | ASW | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA20905 | hp2 | a0001 | c0001 | t0021 | g0162 | SAS | GIH | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0188 | 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 | g0171 | 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 | g0112 | 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 | g0157 | 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 | g0119 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0099 | REF | REF | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0070 | REF | REF | MOB1B_chr4_70897369_70993168 | MOB1B | chr4 | 70897369 | 70993168 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(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 | a0001c0001t0006 a0001c0001t0024 a0001c0002t0006 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(21): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): 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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(8): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0022 |
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 | a0001c0001t0018 a0001c0001t0023 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): 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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(8): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0018 a0001c0001t0023 |
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 | a0001c0001t0019 a0001c0001t0024 |
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 | a0001c0001t0007 a0001c0001t0015 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70902602 | C | CCCGCCCG | 64 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0002g0004 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0008g0262 a0001c0001t0008g0263 a0001c0001t0008g0264 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0260 a0001c0001t0020g0261 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0077 others(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 | 151 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0098 others(148): Show |
151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): 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 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0230 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | |||||||
| chr4:70904584 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0072 a0001c0001t0002g0048 a0001c0001t0004g0267 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0259 |
3 | HG01258.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.14+2487C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70905037 | |||||||
| chr4:70905046 | T | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0081 others(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 | a0001c0001t0004g0273 a0001c0001t0004g0282 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0066 others(162): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0002g0013 a0001c0001t0002g0041 a0001c0001t0002g0042 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0003g0221 a0001c0001t0003g0222 |
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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0081 others(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 | a0001c0001t0002g0004 a0001c0001t0013g0212 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0006g0053 a0001c0001t0006g0061 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(243): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(244): 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 | 274 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(271): Show |
275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): 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 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0005g0078 a0001c0001t0005g0103 a0001c0001t0005g0104 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0005g0103 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0194 a0001c0001t0002g0004 a0001c0001t0002g0005 others(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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(180): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(181): 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 | a0001c0001t0001g0195 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(146): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.14+8525C>T | MOB1B | ENSG00000173542.9 | transcript | ENST00000309395.7 | protein_coding | 1/5 | chr4 | 70911075 | |||||||
| chr4:70911218 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0068 others(79): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(80): 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0122 a0001c0001t0002g0017 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0260 a0001c0001t0020g0261 |
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 | a0001c0001t0001g0150 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | 245 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(242): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0002g0009 a0001c0001t0006g0047 a0001c0001t0006g0049 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(162): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0003g0076 a0001c0001t0003g0089 a0001c0001t0003g0095 others(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 | |||||||
| chr4:70914387 | CT | C | 7 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(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 | a0001c0001t0004g0069 a0001c0001t0004g0079 a0001c0001t0004g0080 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0122 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0196 | 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 | 280 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): 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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0006g0047 a0001c0001t0006g0053 a0001c0001t0006g0057 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0150 a0001c0001t0001g0198 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0003g0075 a0001c0001t0003g0082 a0001c0001t0003g0088 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | 184 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(181): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(182): 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 81 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0068 others(78): Show |
82 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(79): 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0253 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0002g0020 a0001c0001t0002g0048 |
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 | a0001c0001t0010g0006 a0001c0001t0010g0015 |
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 | a0001c0001t0007g0278 a0001c0001t0007g0281 |
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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0260 a0001c0001t0020g0261 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0128 | 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 | a0001c0001t0005g0203 | 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 280 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): 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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0137 a0001c0001t0001g0238 |
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 | a0001c0001t0002g0009 a0001c0001t0006g0047 a0001c0001t0006g0049 others(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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0001g0239 a0001c0001t0001g0242 |
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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0122 others(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 |
173 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0066 others(170): Show |
174 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(171): 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 | a0001c0001t0001g0054 a0001c0001t0001g0121 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0100 a0001c0001t0001g0108 a0001c0001t0001g0234 others(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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0185 | 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 | a0001c0001t0008g0010 a0001c0001t0008g0084 a0001c0001t0008g0224 others(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 | a0001c0001t0002g0009 a0001c0001t0006g0047 a0001c0001t0006g0049 others(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 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(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 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0128 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0021 |
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 | a0001c0001t0002g0020 a0001c0001t0002g0038 a0001c0001t0002g0048 |
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 | a0001c0001t0014g0204 | 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 | a0001c0001t0008g0262 a0001c0001t0008g0263 a0001c0001t0008g0264 |
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 | a0001c0001t0001g0150 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | |||||||
| chr4:70923940 | C | CA | 99 | a0001c0001t0001g0129 a0001c0001t0001g0156 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0198 | 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 | 177 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(174): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0004g0069 a0001c0001t0004g0079 a0001c0001t0004g0080 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0053 a0001c0001t0006g0057 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0005g0203 | 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 | a0001c0001t0003g0085 a0001c0001t0003g0225 |
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 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0005g0208 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0008g0010 a0001c0001t0008g0084 a0001c0001t0008g0224 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0001g0132 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0260 a0001c0001t0020g0261 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0005g0209 | 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(248): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): 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 | a0001c0001t0005g0205 | 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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(232): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(233): 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 | a0001c0001t0005g0205 | 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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0021g0162 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0003g0221 a0001c0001t0003g0222 |
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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(248): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0184 a0001c0001t0002g0029 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0196 |
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 | 214 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): 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 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0002g0004 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0002g0016 a0001c0001t0002g0021 |
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 | a0001c0001t0003g0085 a0001c0001t0003g0225 a0001c0001t0007g0275 others(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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(161): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): 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 | a0001c0001t0005g0203 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0132 a0001c0001t0001g0154 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | |||||||
| chr4:70929879 | C | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0225 |
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 | |||||||
| chr4:70930498 | G | A | 1 | a0001c0001t0008g0071 | 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 | a0001c0001t0003g0076 a0001c0001t0003g0082 a0001c0001t0003g0088 others(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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0066 others(157): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): 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 | a0001c0001t0001g0054 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0260 a0001c0001t0020g0261 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0005g0104 a0001c0001t0005g0202 a0001c0001t0005g0209 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0005g0208 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0171 a0001c0001t0004g0267 a0001c0001t0004g0268 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0100 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0110 a0001c0001t0001g0125 others(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 | a0001c0001t0004g0080 a0001c0001t0004g0267 a0001c0001t0004g0268 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(241): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(242): 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 | a0001c0001t0001g0108 a0001c0001t0004g0067 a0001c0001t0004g0069 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | 141 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0068 others(138): Show |
142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): 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 | a0001c0001t0001g0066 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0007g0276 a0001c0001t0007g0280 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0198 | 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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0005g0211 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0010g0006 a0001c0001t0010g0015 |
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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(232): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(233): 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0005g0211 a0001c0001t0006g0047 a0001c0001t0006g0049 others(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 | a0001c0001t0004g0269 a0001c0001t0004g0274 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0242 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0098 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0218 a0001c0001t0018g0002 others(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 | 69 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0102 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(66): 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 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0155 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0133 a0001c0001t0003g0095 a0001c0001t0003g0226 others(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 | a0001c0001t0007g0276 a0001c0001t0007g0279 a0001c0001t0011g0265 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0122 | 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 | 280 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): 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 | 218 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(215): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): 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 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0001c0001t0001g0200 others(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 | a0001c0001t0002g0019 a0001c0001t0005g0078 a0001c0001t0005g0103 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0009g0178 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | |||||||
| chr4:70939659 | G | A | 7 | a0001c0001t0006g0047 a0001c0001t0006g0053 a0001c0001t0006g0057 others(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 | a0001c0001t0004g0273 a0001c0001t0004g0282 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0004g0080 a0001c0001t0004g0081 |
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 | a0001c0001t0006g0064 a0001c0001t0024g0063 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0143 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0002g0056 a0001c0001t0007g0275 a0001c0001t0007g0276 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0146 a0001c0001t0001g0149 others(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 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(248): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): 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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0277 a0001c0001t0007g0278 others(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 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(162): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0012g0176 | 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 | a0001c0001t0006g0049 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0001g0124 a0001c0001t0001g0145 |
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 | a0001c0001t0009g0179 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0100 others(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 | |||||||
| chr4:70945719 | A | C | 2 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
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 | a0001c0001t0001g0246 a0001c0001t0006g0047 a0001c0001t0006g0049 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0278 others(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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(208): Show |
212 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(209): 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 | a0001c0001t0008g0071 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0004g0080 a0001c0001t0004g0081 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0062 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0005g0207 a0001c0001t0005g0256 |
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 | a0001c0001t0001g0124 | 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 | a0001c0001t0005g0208 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0008g0071 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0225 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0267 a0001c0001t0004g0268 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0021g0162 | 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 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0008g0071 | 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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0270 | 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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0239 a0001c0001t0001g0242 |
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 | a0001c0001t0006g0051 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0190 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0053 a0001c0001t0006g0057 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0144 |
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 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0036 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0001c0001t0002g0046 |
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 | a0001c0001t0001g0128 | 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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0239 a0001c0001t0002g0023 a0001c0001t0002g0031 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0143 | 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 | 37 | a0001c0001t0001g0068 a0001c0001t0001g0102 a0001c0001t0001g0106 others(34): Show |
37 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(34): 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 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0082 a0001c0001t0003g0085 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0277 |
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 | a0001c0001t0001g0106 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0008g0010 a0001c0001t0008g0084 a0001c0001t0008g0224 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0006g0057 a0001c0001t0006g0060 |
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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0062 a0001c0001t0002g0004 a0001c0001t0002g0005 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0196 |
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 | a0001c0001t0001g0183 | 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0008g0262 a0001c0001t0008g0263 a0001c0001t0008g0264 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0008g0071 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0239 a0001c0001t0001g0241 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0137 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0122 others(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 | a0001c0001t0006g0049 a0001c0001t0006g0050 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0120 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0197 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0005g0104 a0001c0001t0005g0202 a0001c0001t0005g0209 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0005g0210 | 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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0150 | 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 | a0001c0001t0002g0028 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0009g0178 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0150 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0048 a0001c0001t0004g0282 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0239 a0001c0001t0001g0241 others(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 | a0001c0001t0003g0075 a0001c0001t0007g0275 a0001c0001t0007g0276 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0164 |
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 | 1 | a0001c0001t0001g0218 | 1 | HG01258.hp2 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0196 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0003g0221 a0001c0001t0003g0222 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0145 |
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 | 216 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0072 others(213): Show |
216 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(213): 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0076 a0001c0001t0003g0089 |
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 | a0001c0001t0003g0076 a0001c0001t0003g0089 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0260 a0001c0001t0020g0261 |
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 | a0001c0001t0005g0203 a0001c0001t0005g0208 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0129 a0001c0001t0001g0131 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0169 a0001c0001t0001g0244 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0006g0049 a0001c0001t0006g0050 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0008g0071 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0194 a0001c0001t0001g0199 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0040 a0001c0001t0002g0044 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0111 a0001c0001t0001g0113 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0278 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0113 a0001c0001t0001g0129 others(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 | a0001c0001t0004g0069 a0001c0001t0004g0080 a0001c0001t0004g0081 others(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 | a0001c0001t0003g0082 a0001c0001t0003g0088 a0001c0001t0003g0089 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0002g0043 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0005g0203 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0195 |
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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0267 a0001c0001t0004g0268 others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0137 a0001c0001t0001g0238 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0276 a0001c0001t0007g0279 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0001g0139 a0001c0001t0001g0168 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0142 a0001c0001t0001g0196 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | 74 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0068 others(71): Show |
75 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(72): 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 | a0001c0001t0002g0004 a0001c0001t0004g0273 a0001c0001t0008g0010 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0164 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0239 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0005g0104 a0001c0001t0005g0202 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0196 |
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 | a0001c0001t0006g0053 a0001c0001t0006g0061 |
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 | a0001c0001t0001g0066 a0001c0001t0001g0109 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0154 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0090 a0001c0001t0003g0221 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0225 |
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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0040 a0001c0001t0002g0056 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0256 |
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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0004g0273 a0001c0001t0004g0282 |
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 | a0001c0001t0001g0155 | 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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0049 a0001c0001t0006g0050 others(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 | a0001c0001t0002g0022 a0001c0001t0002g0026 a0001c0001t0002g0030 |
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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0005g0104 a0001c0001t0005g0208 a0001c0001t0008g0224 |
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 | a0001c0001t0006g0049 | 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 | a0001c0001t0006g0050 a0001c0002t0006g0052 |
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 | a0001c0001t0002g0009 a0001c0001t0006g0051 a0001c0001t0026g0011 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0053 a0001c0001t0006g0057 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0082 others(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 | a0001c0001t0007g0276 a0001c0001t0007g0279 a0001c0001t0007g0280 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0277 a0001c0001t0007g0278 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0180 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0260 a0001c0001t0003g0085 a0001c0001t0003g0086 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0026 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0171 |
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 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 | a0001c0001t0011g0265 a0001c0001t0011g0266 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0256 |
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 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0081 others(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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0100 a0001c0001t0001g0234 |
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 | a0001c0001t0004g0067 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | a0001c0001t0022g0201 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0018g0002 a0001c0001t0023g0003 |
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 | a0001c0001t0001g0113 a0001c0001t0002g0004 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0009 a0001c0001t0026g0011 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0041 a0001c0001t0002g0044 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0256 |
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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0007g0275 a0001c0001t0007g0276 a0001c0001t0007g0277 others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0008g0010 a0001c0001t0008g0071 a0001c0001t0008g0084 others(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 | a0001c0001t0002g0009 a0001c0001t0026g0011 |
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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(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 |