Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10651 |
| ensemblid | ENSG00000128654.14 |
| hgncid | 7506 |
| symbol | MTX2 |
| name | metaxin 2 |
| refseq_nuc | NM_006554.5 |
| refseq_prot | NP_006545.1 |
| ensembl_nuc | ENST00000249442.11 |
| ensembl_prot | ENSP00000249442.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 176269442 |
| end | 176338025 |
| strand | + |
| ver | v1.2 |
| region | chr2:176269442-176338025 |
| region5000 | chr2:176264442-176343025 |
| regionname0 | MTX2_chr2_176269442_176338025 |
| regionname5000 | MTX2_chr2_176264442_176343025 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 263 | 334 | 93 | 66 | 133 | 12 | 28 | 110 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| a0002 | 0/0 | 263 | 9 | 0 | 0 | 9 | 0 | 0 | 6 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| a0003 | 0/0 | 263 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| a0004 | 0/0 | 263 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| a0005 | 0/0 | 263 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| a0006 | 0/0 | 263 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| a0007 | 0/0 | 263 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | MSLVA others(258): Show |
chr2 | 176264442 | 176343025 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 789 | 333 | 92 | 66 | 133 | 12 | 28 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0001c0006 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0002c0002 | 0/0 | 789 | 9 | 0 | 0 | 9 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0003c0008 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0004c0003 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0005c0004 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0006c0007 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 | ||
| a0007c0005 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | ATGTC others(784): Show |
chr2 | 176264442 | 176343025 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1341 | 230 | 61 | 38 | 101 | 11 | 17 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0001c0001t0002 | 0/0 | 1341 | 84 | 19 | 25 | 32 | 1 | 7 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0001c0001t0004 | 0/0 | 1341 | 7 | 5 | 2 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0001c0001t0005 | 0/0 | 1338 | 6 | 5 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1333): Show |
chr2 | 176264442 | 176343025 |
| a0001c0001t0006 | 0/0 | 1341 | 4 | 0 | 0 | 0 | 0 | 4 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0001c0001t0007 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0001c0001t0008 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1333): Show |
chr2 | 176264442 | 176343025 |
| a0001c0006t0001 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0002c0002t0003 | 0/0 | 1341 | 9 | 0 | 0 | 9 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0003c0008t0002 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0004c0003t0001 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0005c0004t0002 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTTCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0006c0007t0001 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| a0007c0005t0001 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | GTCCC others(1336): Show |
chr2 | 176264442 | 176343025 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 15 | 0 | 2 | 10 | 1 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0006g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0001c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0003c0008t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0004c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0005c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0006c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| a0007c0005t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0237 | EUR | FIN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00558 | hp2 | a0003 | c0008 | t0002 | g0233 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00673 | hp1 | a0004 | c0003 | t0001 | g0158 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0226 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02040 | hp2 | a0002 | c0002 | t0003 | g0042 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0041 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02976 | hp2 | a0001 | c0006 | t0001 | g0023 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03209 | hp1 | a0005 | c0004 | t0002 | g0222 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0017 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0017 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0240 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | STU | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0239 | SAS | STU | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | YRI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0043 | EAS | CHB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | YRI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18954 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0229 | AFR | LWK | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | LWK | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19078 | hp2 | a0006 | c0007 | t0001 | g0152 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19080 | hp2 | a0007 | c0005 | t0001 | g0186 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19086 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ASW | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | USA | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | USA | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA18955 | hp2 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | LWK | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0163 | REF | REF | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | MTX2_chr2_176264442_176343025 | MTX2 | chr2 | 176264442 | 176343025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:176326870 | T | C | 1 | a0004 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.254T>C | p.Leu85Pro | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/10 | 442/1341 | 254/792 | 85/263 | chr2 | 176326870 | |||
| chr2:176326878 | A | G | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.262A>G | p.Ile88Val | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/10 | 450/1341 | 262/792 | 88/263 | chr2 | 176326878 | |||
| chr2:176328297 | A | G | 1 | a0006 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.290A>G | p.His97Arg | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 6/10 | 478/1341 | 290/792 | 97/263 | chr2 | 176328297 | |||
| chr2:176328359 | G | A | 1 | a0002 | 9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
missense_variant | MODERATE | c.352G>A | p.Val118Ile | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 6/10 | 540/1341 | 352/792 | 118/263 | chr2 | 176328359 | |||
| chr2:176337533 | A | G | 1 | a0007 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.661A>G | p.Thr221Ala | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 849/1341 | 661/792 | 221/263 | chr2 | 176337533 | |||
| chr2:176337593 | A | G | 1 | a0005 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.721A>G | p.Asn241Asp | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 909/1341 | 721/792 | 241/263 | chr2 | 176337593 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:176337508 | C | T | 1 | a0001c0006 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.636C>T | p.Asp212Asp | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 824/1341 | 636/792 | 212/263 | chr2 | 176337508 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:176269444 | C | T | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(4): Show |
106 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-186C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/10 | 186 | chr2 | 176269444 | ||||||
| chr2:176269563 | G | C | 1 | a0002c0002t0003 | 9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/10 | 67 | chr2 | 176269563 | ||||||
| chr2:176269609 | G | A | 1 | a0001c0001t0006 | 4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-21G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/10 | 21 | chr2 | 176269609 | ||||||
| chr2:176337670 | T | A | 1 | a0001c0001t0008 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 6 | chr2 | 176337670 | ||||||
| chr2:176337786 | A | G | 1 | a0001c0001t0007 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 122 | chr2 | 176337786 | ||||||
| chr2:176337810 | ATTG | A | 2 | a0001c0001t0005 a0001c0001t0008 |
7 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*149_*151delGTT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 149 | INFO_REALIGN_3_PRIME | chr2 | 176337810 | |||||
| chr2:176337904 | A | G | 1 | a0001c0001t0004 | 7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*240A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 10/10 | 240 | chr2 | 176337904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:176269812 | A | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+143A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176269812 | |||||||
| chr2:176269845 | G | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.40+176G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176269845 | |||||||
| chr2:176269859 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+190G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176269859 | |||||||
| chr2:176269883 | C | A | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+214C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176269883 | |||||||
| chr2:176269992 | A | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+323A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176269992 | |||||||
| chr2:176270147 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.40+478A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270147 | |||||||
| chr2:176270185 | G | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+516G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270185 | |||||||
| chr2:176270232 | A | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+563A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270232 | |||||||
| chr2:176270329 | C | A | 1 | a0001c0001t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.40+660C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270329 | |||||||
| chr2:176270505 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 |
4 | NA18982.hp1 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+836G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270505 | |||||||
| chr2:176270568 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+899A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270568 | |||||||
| chr2:176270745 | A | G | 92 | a0001c0001t0001g0235 a0001c0001t0001g0300 a0001c0001t0001g0301 others(89): Show |
104 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.40+1076A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270745 | |||||||
| chr2:176270747 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.40+1078A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270747 | |||||||
| chr2:176270778 | C | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+1109C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270778 | |||||||
| chr2:176270836 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.40+1167T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270836 | |||||||
| chr2:176270913 | T | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+1244T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176270913 | |||||||
| chr2:176271552 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+1883T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176271552 | |||||||
| chr2:176271756 | G | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(54): Show |
67 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.40+2087G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176271756 | |||||||
| chr2:176271802 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+2133A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176271802 | |||||||
| chr2:176271920 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.40+2251G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176271920 | |||||||
| chr2:176272456 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40+2787A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176272456 | |||||||
| chr2:176272761 | G | A | 74 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(71): Show |
86 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.40+3092G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176272761 | |||||||
| chr2:176273115 | G | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+3446G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176273115 | |||||||
| chr2:176273402 | T | A | 112 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(109): Show |
126 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.40+3733T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176273402 | |||||||
| chr2:176273672 | A | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG02071.hp2 NA18954.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+4003A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176273672 | |||||||
| chr2:176273718 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.40+4049G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176273718 | |||||||
| chr2:176273727 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.40+4058T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176273727 | |||||||
| chr2:176273913 | T | TA | 62 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(59): Show |
72 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.40+4257dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176273913 | ||||||
| chr2:176273913 | TA | T | 15 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+4257delA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176273913 | ||||||
| chr2:176274042 | G | C | 74 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(71): Show |
86 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.40+4373G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274042 | |||||||
| chr2:176274272 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.40+4603A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274272 | |||||||
| chr2:176274400 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+4731A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274400 | |||||||
| chr2:176274488 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(54): Show |
67 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.40+4819G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274488 | |||||||
| chr2:176274507 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.40+4838A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274507 | |||||||
| chr2:176274546 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | HG01361.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.40+4877C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274546 | |||||||
| chr2:176274663 | G | T | 5 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0284 others(2): Show |
5 | NA18966.hp2 NA18993.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+4994G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274663 | |||||||
| chr2:176274721 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.40+5052C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274721 | |||||||
| chr2:176274810 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.40+5141A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274810 | |||||||
| chr2:176274942 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.40+5273C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274942 | |||||||
| chr2:176274999 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.40+5330G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176274999 | |||||||
| chr2:176275044 | G | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+5375G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275044 | |||||||
| chr2:176275241 | A | AT | 9 | a0001c0001t0001g0025 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02055.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.40+5586dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176275241 | ||||||
| chr2:176275319 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.40+5650A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275319 | |||||||
| chr2:176275362 | T | G | 127 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(124): Show |
142 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.40+5693T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275362 | |||||||
| chr2:176275498 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.40+5829C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275498 | |||||||
| chr2:176275576 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.40+5907T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275576 | |||||||
| chr2:176275635 | A | C | 100 | a0001c0001t0001g0235 a0001c0001t0001g0300 a0001c0001t0001g0301 others(97): Show |
112 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.40+5966A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275635 | |||||||
| chr2:176275659 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+5990C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275659 | |||||||
| chr2:176275711 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.40+6042T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275711 | |||||||
| chr2:176275983 | G | T | 1 | a0001c0001t0002g0286 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.40+6314G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176275983 | |||||||
| chr2:176276111 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+6442G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176276111 | |||||||
| chr2:176276152 | A | G | 7 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(4): Show |
7 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+6483A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176276152 | |||||||
| chr2:176276170 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.40+6501A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176276170 | |||||||
| chr2:176276280 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+6611A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176276280 | |||||||
| chr2:176276817 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+7148C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176276817 | |||||||
| chr2:176276978 | CGTT | C | 3 | a0001c0001t0006g0017 a0001c0001t0006g0239 a0001c0001t0006g0240 |
4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+7312_40+7314del others(3): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176276978 | ||||||
| chr2:176277092 | C | T | 22 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0267 others(19): Show |
24 | HG00408.hp2 HG02040.hp1 HG02602.hp1 others(21): Show |
intron_variant | MODIFIER | c.40+7423C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277092 | |||||||
| chr2:176277100 | C | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG00280.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.40+7431C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277100 | |||||||
| chr2:176277152 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+7483T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277152 | |||||||
| chr2:176277434 | C | T | 2 | a0001c0001t0002g0223 a0005c0004t0002g0222 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.40+7765C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277434 | |||||||
| chr2:176277488 | C | T | 1 | a0002c0002t0003g0044 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.40+7819C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277488 | |||||||
| chr2:176277489 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.40+7820G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277489 | |||||||
| chr2:176277560 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+7891A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277560 | |||||||
| chr2:176277817 | G | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+8148G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277817 | |||||||
| chr2:176277849 | T | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+8180T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277849 | |||||||
| chr2:176277977 | T | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+8308T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176277977 | |||||||
| chr2:176278041 | G | GT | 84 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0023 others(81): Show |
86 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.40+8399dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176278041 | ||||||
| chr2:176278041 | G | GTT | 14 | a0001c0001t0001g0047 a0001c0001t0001g0188 a0001c0001t0001g0189 others(11): Show |
15 | HG00639.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+8398_40+8399dup others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176278041 | ||||||
| chr2:176278041 | GT | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0026 others(27): Show |
32 | HG00741.hp2 HG01169.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+8399delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176278041 | ||||||
| chr2:176278041 | GTT | G | 67 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0019 others(64): Show |
78 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.40+8398_40+8399del others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176278041 | ||||||
| chr2:176278041 | GTTT | G | 9 | a0001c0001t0001g0235 a0001c0001t0002g0018 a0001c0001t0002g0231 others(6): Show |
10 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.40+8397_40+8399del others(3): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176278041 | ||||||
| chr2:176278041 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.40+8390_40+8399del others(10): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176278041 | ||||||
| chr2:176278134 | T | C | 1 | a0001c0001t0005g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.40+8465T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278134 | |||||||
| chr2:176278136 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.40+8467T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278136 | |||||||
| chr2:176278239 | C | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+8570C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278239 | |||||||
| chr2:176278760 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0001t0002g0219 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+9091C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278760 | |||||||
| chr2:176278796 | T | A | 109 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(106): Show |
123 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.40+9127T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278796 | |||||||
| chr2:176278821 | A | G | 95 | a0001c0001t0001g0235 a0001c0001t0002g0002 a0001c0001t0002g0004 others(92): Show |
107 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.40+9152A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278821 | |||||||
| chr2:176278841 | A | G | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+9172A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176278841 | |||||||
| chr2:176279046 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+9377G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279046 | |||||||
| chr2:176279168 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.40+9499A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279168 | |||||||
| chr2:176279202 | A | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.40+9533A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279202 | |||||||
| chr2:176279249 | T | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.40+9580T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279249 | |||||||
| chr2:176279262 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.40+9593A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279262 | |||||||
| chr2:176279268 | T | A | 1 | a0001c0001t0002g0286 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.40+9599T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279268 | |||||||
| chr2:176279301 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(50): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.40+9632A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279301 | |||||||
| chr2:176279962 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.40+10293A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176279962 | |||||||
| chr2:176280303 | T | A | 86 | a0001c0001t0001g0235 a0001c0001t0002g0002 a0001c0001t0002g0004 others(83): Show |
98 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.40+10634T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176280303 | |||||||
| chr2:176280354 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0164 |
2 | HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.40+10685C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176280354 | |||||||
| chr2:176280558 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.40+10889C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176280558 | |||||||
| chr2:176280649 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+10980T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176280649 | |||||||
| chr2:176280711 | C | T | 14 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(11): Show |
16 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+11042C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176280711 | |||||||
| chr2:176281042 | T | A | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.40+11373T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281042 | |||||||
| chr2:176281217 | T | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(55): Show |
68 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.40+11548T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281217 | |||||||
| chr2:176281224 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.40+11555C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281224 | |||||||
| chr2:176281363 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
5 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+11694G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281363 | |||||||
| chr2:176281477 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40+11808A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281477 | |||||||
| chr2:176281547 | T | C | 98 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(95): Show |
110 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.40+11878T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281547 | |||||||
| chr2:176281772 | A | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.40+12103A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281772 | |||||||
| chr2:176281780 | G | C | 1 | a0001c0001t0004g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40+12111G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281780 | |||||||
| chr2:176281820 | G | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+12151G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281820 | |||||||
| chr2:176281834 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.40+12165T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281834 | |||||||
| chr2:176281963 | A | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+12294A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176281963 | |||||||
| chr2:176282122 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.40+12453A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282122 | |||||||
| chr2:176282126 | G | GT | 101 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.40+12485dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTT | 40 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0046 others(37): Show |
41 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.40+12484_40+12485d others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
15 | HG01515.hp2 HG02074.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+12483_40+12485d others(5): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT | 7 | a0001c0001t0001g0235 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+12479_40+12485d others(9): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0002g0241 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.40+12464_40+12465i others(12): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0002g0243 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.40+12465_40+12466i others(12): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(4): Show |
32 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(29): Show |
43 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.40+12465_40+12466i others(13): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(5): Show |
29 | a0001c0001t0002g0020 a0001c0001t0002g0218 a0001c0001t0002g0219 others(26): Show |
30 | HG00408.hp2 HG00733.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.40+12465_40+12466i others(14): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(6): Show |
4 | a0001c0001t0002g0215 a0001c0001t0002g0259 a0001c0001t0002g0266 others(1): Show |
4 | HG00741.hp2 HG02071.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+12465_40+12466i others(15): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(7): Show |
3 | a0001c0001t0002g0033 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02615.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.40+12465_40+12466i others(16): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0002g0034 a0001c0001t0002g0036 a0001c0001t0002g0221 |
3 | HG02055.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.40+12465_40+12466i others(17): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.40+12465_40+12466i others(18): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40+12475_40+12485d others(13): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0002g0260 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.40+12474_40+12485d others(14): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | GTTTT | G | 8 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(5): Show |
8 | HG02040.hp2 HG02083.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+12482_40+12485d others(6): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282126 | GTTTTTTT others(4): Show |
G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.40+12475_40+12485d others(13): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282126 | ||||||
| chr2:176282130 | T | TTTTTGTT others(5): Show |
1 | a0001c0001t0002g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.40+12465_40+12466i others(14): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282130 | ||||||
| chr2:176282133 | T | TTGTTTTT others(4): Show |
1 | a0001c0001t0002g0267 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.40+12465_40+12466i others(13): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282133 | ||||||
| chr2:176282134 | T | TGTTTTTT others(4): Show |
1 | a0001c0001t0002g0268 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.40+12465_40+12466i others(13): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282134 | |||||||
| chr2:176282136 | T | G | 1 | a0001c0001t0005g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+12467T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282136 | |||||||
| chr2:176282186 | A | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+12517A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282186 | |||||||
| chr2:176282216 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.40+12547T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282216 | |||||||
| chr2:176282405 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+12736C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282405 | |||||||
| chr2:176282468 | A | G | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+12799A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282468 | |||||||
| chr2:176282706 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.40+13037T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282706 | |||||||
| chr2:176282707 | T | G | 111 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(108): Show |
123 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.40+13038T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282707 | |||||||
| chr2:176282710 | G | GT | 24 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0107 others(21): Show |
25 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.40+13052dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176282710 | ||||||
| chr2:176282903 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
5 | NA18964.hp1 NA18980.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+13234C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282903 | |||||||
| chr2:176282930 | C | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+13261C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176282930 | |||||||
| chr2:176283240 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+13571C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176283240 | |||||||
| chr2:176283427 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-13433C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176283427 | |||||||
| chr2:176283623 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.41-13237A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176283623 | |||||||
| chr2:176283631 | T | C | 99 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(96): Show |
111 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.41-13229T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176283631 | |||||||
| chr2:176283636 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.41-13224A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176283636 | |||||||
| chr2:176283993 | A | G | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(125): Show |
143 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.41-12867A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176283993 | |||||||
| chr2:176284257 | T | A | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-12603T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284257 | |||||||
| chr2:176284332 | A | G | 7 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(4): Show |
7 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-12528A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284332 | |||||||
| chr2:176284389 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41-12471T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284389 | |||||||
| chr2:176284656 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 |
4 | NA18982.hp1 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-12204A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284656 | |||||||
| chr2:176284788 | T | C | 11 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0242 others(8): Show |
16 | HG00642.hp2 HG01099.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-12072T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284788 | |||||||
| chr2:176284797 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-12063A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284797 | |||||||
| chr2:176284914 | T | G | 1 | a0001c0001t0001g0299 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-11946T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284914 | |||||||
| chr2:176284930 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.41-11930A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176284930 | |||||||
| chr2:176285286 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41-11574T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285286 | |||||||
| chr2:176285343 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.41-11517A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285343 | |||||||
| chr2:176285372 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0160 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.41-11488A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285372 | |||||||
| chr2:176285418 | C | CT | 82 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0025 others(79): Show |
85 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.41-11423dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176285418 | ||||||
| chr2:176285418 | C | CTT | 8 | a0001c0001t0001g0059 a0001c0001t0001g0162 a0002c0002t0003g0039 others(5): Show |
8 | HG02040.hp2 HG02083.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-11424_41-11423d others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176285418 | ||||||
| chr2:176285418 | CT | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0029 others(29): Show |
40 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.41-11423delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176285418 | ||||||
| chr2:176285513 | A | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-11347A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285513 | |||||||
| chr2:176285637 | C | CT | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-11211dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176285637 | ||||||
| chr2:176285649 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-11211T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285649 | |||||||
| chr2:176285783 | C | T | 10 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0242 others(7): Show |
15 | HG00642.hp2 HG01099.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-11077C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285783 | |||||||
| chr2:176285913 | G | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-10947G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285913 | |||||||
| chr2:176285964 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41-10896C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176285964 | |||||||
| chr2:176286147 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.41-10713G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286147 | |||||||
| chr2:176286329 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-10531T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286329 | |||||||
| chr2:176286483 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.41-10377G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286483 | |||||||
| chr2:176286514 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.41-10346A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286514 | |||||||
| chr2:176286550 | C | CT | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
14 | HG01175.hp1 HG02040.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-10296dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176286550 | ||||||
| chr2:176286713 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-10147C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286713 | |||||||
| chr2:176286828 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-10032C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286828 | |||||||
| chr2:176286996 | C | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.41-9864C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176286996 | |||||||
| chr2:176287615 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(227): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.41-9245G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176287615 | |||||||
| chr2:176287687 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.41-9173T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176287687 | |||||||
| chr2:176287888 | TACTG | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-8967_41-8964del others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176287888 | ||||||
| chr2:176287897 | C | CT | 7 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0139 others(4): Show |
8 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-8948dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176287897 | ||||||
| chr2:176287897 | CT | C | 85 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0113 others(82): Show |
97 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.41-8948delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176287897 | ||||||
| chr2:176287912 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.41-8948T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176287912 | |||||||
| chr2:176287932 | A | G | 58 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(55): Show |
68 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.41-8928A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176287932 | |||||||
| chr2:176287981 | AAACACTG others(4): Show |
A | 72 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(69): Show |
84 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.41-8878_41-8868del others(11): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176287981 | |||||||
| chr2:176288192 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-8668C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288192 | |||||||
| chr2:176288228 | ATAAAGTC others(22): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.41-8627_41-8599del others(29): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176288228 | ||||||
| chr2:176288394 | T | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-8466T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288394 | |||||||
| chr2:176288421 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.41-8439C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288421 | |||||||
| chr2:176288538 | C | G | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.41-8322C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288538 | |||||||
| chr2:176288591 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.41-8269A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288591 | |||||||
| chr2:176288634 | A | T | 1 | a0001c0001t0001g0012 | 2 | NA18993.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.41-8226A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288634 | |||||||
| chr2:176288659 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.41-8201T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288659 | |||||||
| chr2:176288804 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-8056A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288804 | |||||||
| chr2:176288839 | C | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | HG02280.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-8021C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176288839 | |||||||
| chr2:176289116 | GT | G | 86 | a0001c0001t0001g0235 a0001c0001t0002g0002 a0001c0001t0002g0004 others(83): Show |
98 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.41-7736delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176289116 | ||||||
| chr2:176289207 | C | T | 74 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(71): Show |
86 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.41-7653C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289207 | |||||||
| chr2:176289369 | A | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-7491A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289369 | |||||||
| chr2:176289420 | A | G | 93 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(90): Show |
105 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.41-7440A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289420 | |||||||
| chr2:176289493 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.41-7367T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289493 | |||||||
| chr2:176289500 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-7360C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289500 | |||||||
| chr2:176289656 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.41-7204A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289656 | |||||||
| chr2:176289666 | G | A | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(125): Show |
143 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.41-7194G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289666 | |||||||
| chr2:176289688 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-7172G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289688 | |||||||
| chr2:176289830 | A | C | 11 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0001g0174 others(8): Show |
11 | HG00408.hp1 HG01261.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-7030A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289830 | |||||||
| chr2:176289940 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41-6920A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176289940 | |||||||
| chr2:176290157 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-6703C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176290157 | |||||||
| chr2:176290345 | G | T | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-6515G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176290345 | |||||||
| chr2:176290577 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-6283A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176290577 | |||||||
| chr2:176290696 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01071.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.41-6164A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176290696 | |||||||
| chr2:176290742 | T | C | 11 | a0001c0001t0001g0235 a0001c0001t0002g0033 a0001c0001t0002g0034 others(8): Show |
11 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-6118T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176290742 | |||||||
| chr2:176290748 | G | GT | 76 | a0001c0001t0001g0111 a0001c0001t0001g0137 a0001c0001t0002g0002 others(73): Show |
88 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.41-6095dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176290748 | ||||||
| chr2:176290832 | C | CAT | 98 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(95): Show |
110 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.41-6026_41-6025dup others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176290832 | ||||||
| chr2:176290849 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.41-6011T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176290849 | |||||||
| chr2:176291063 | G | A | 1 | a0001c0001t0005g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.41-5797G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291063 | |||||||
| chr2:176291111 | G | C | 1 | a0001c0001t0002g0232 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.41-5749G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291111 | |||||||
| chr2:176291309 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.41-5551C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291309 | |||||||
| chr2:176291449 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.41-5411C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291449 | |||||||
| chr2:176291471 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.41-5389C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291471 | |||||||
| chr2:176291624 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.41-5236G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291624 | |||||||
| chr2:176291666 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(33): Show |
37 | HG00408.hp1 HG00597.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.41-5194A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291666 | |||||||
| chr2:176291725 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-5135G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291725 | |||||||
| chr2:176291748 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41-5112G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291748 | |||||||
| chr2:176291887 | G | C | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-4973G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176291887 | |||||||
| chr2:176292059 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.41-4801G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176292059 | |||||||
| chr2:176292100 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41-4760A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176292100 | |||||||
| chr2:176292244 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41-4616G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176292244 | |||||||
| chr2:176292340 | A | T | 11 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0001g0174 others(8): Show |
11 | HG00408.hp1 HG01261.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-4520A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176292340 | |||||||
| chr2:176292439 | CTT | C | 85 | a0001c0001t0001g0235 a0001c0001t0002g0002 a0001c0001t0002g0004 others(82): Show |
97 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.41-4418_41-4417del others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176292439 | ||||||
| chr2:176292655 | C | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
11 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-4205C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176292655 | |||||||
| chr2:176292843 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.41-4017A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176292843 | |||||||
| chr2:176293053 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.41-3807G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293053 | |||||||
| chr2:176293458 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.41-3402G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293458 | |||||||
| chr2:176293524 | T | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-3336T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293524 | |||||||
| chr2:176293577 | G | A | 85 | a0001c0001t0001g0235 a0001c0001t0002g0002 a0001c0001t0002g0004 others(82): Show |
97 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.41-3283G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293577 | |||||||
| chr2:176293588 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.41-3272C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293588 | |||||||
| chr2:176293589 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | HG02280.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-3271C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293589 | |||||||
| chr2:176293694 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | NA18941.hp1 NA18970.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3166C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293694 | |||||||
| chr2:176293712 | T | C | 1 | a0005c0004t0002g0222 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.41-3148T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293712 | |||||||
| chr2:176293731 | A | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-3129A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293731 | |||||||
| chr2:176293854 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0153 |
2 | NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.41-3006C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293854 | |||||||
| chr2:176293882 | T | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.41-2978T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293882 | |||||||
| chr2:176293912 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.41-2948C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293912 | |||||||
| chr2:176293914 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.41-2946T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176293914 | |||||||
| chr2:176294278 | C | CT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0059 others(10): Show |
14 | HG01071.hp1 HG01074.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-2561dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176294278 | ||||||
| chr2:176294278 | CT | C | 88 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0092 others(85): Show |
100 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.41-2561delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 176294278 | ||||||
| chr2:176294444 | C | T | 12 | a0001c0001t0001g0143 a0001c0001t0002g0002 a0001c0001t0002g0020 others(9): Show |
17 | HG00642.hp2 HG01099.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-2416C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294444 | |||||||
| chr2:176294521 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-2339C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294521 | |||||||
| chr2:176294526 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.41-2334C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294526 | |||||||
| chr2:176294646 | A | G | 2 | a0001c0001t0002g0263 a0001c0001t0002g0266 |
2 | HG00741.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.41-2214A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294646 | |||||||
| chr2:176294689 | C | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-2171C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294689 | |||||||
| chr2:176294754 | G | A | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-2106G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294754 | |||||||
| chr2:176294760 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0153 |
2 | NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.41-2100C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294760 | |||||||
| chr2:176294981 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-1879C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176294981 | |||||||
| chr2:176295199 | T | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1661T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295199 | |||||||
| chr2:176295264 | G | C | 1 | a0001c0001t0002g0276 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.41-1596G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295264 | |||||||
| chr2:176295291 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.41-1569G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295291 | |||||||
| chr2:176295484 | GC | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-1375delC | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295484 | |||||||
| chr2:176295608 | A | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0181 |
2 | NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.41-1252A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295608 | |||||||
| chr2:176295631 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1229A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295631 | |||||||
| chr2:176295678 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-1182A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295678 | |||||||
| chr2:176295692 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1168T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295692 | |||||||
| chr2:176295792 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-1068G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295792 | |||||||
| chr2:176295943 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | NA18956.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.41-917T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295943 | |||||||
| chr2:176295958 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.41-902A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295958 | |||||||
| chr2:176295966 | T | C | 2 | a0001c0001t0004g0057 a0001c0001t0004g0058 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.41-894T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176295966 | |||||||
| chr2:176296084 | A | T | 7 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(4): Show |
7 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-776A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296084 | |||||||
| chr2:176296086 | T | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
50 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-774T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296086 | |||||||
| chr2:176296128 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.41-732T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296128 | |||||||
| chr2:176296240 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0112 |
2 | HG00438.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.41-620A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296240 | |||||||
| chr2:176296314 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-546C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296314 | |||||||
| chr2:176296329 | G | T | 5 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0251 others(2): Show |
7 | NA18939.hp2 NA18980.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-531G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296329 | |||||||
| chr2:176296400 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-460C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296400 | |||||||
| chr2:176296469 | A | T | 127 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(124): Show |
142 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.41-391A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296469 | |||||||
| chr2:176296570 | G | T | 1 | a0001c0001t0005g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.41-290G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296570 | |||||||
| chr2:176296592 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-268C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296592 | |||||||
| chr2:176296612 | A | G | 1 | a0002c0002t0003g0045 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.41-248A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296612 | |||||||
| chr2:176296736 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.41-124T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296736 | |||||||
| chr2:176296815 | T | C | 7 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(4): Show |
7 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-45T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 1/9 | chr2 | 176296815 | |||||||
| chr2:176296999 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.88+92A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176296999 | |||||||
| chr2:176297110 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.88+203T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297110 | |||||||
| chr2:176297327 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0138 a0001c0001t0001g0141 others(5): Show |
8 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+420C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297327 | |||||||
| chr2:176297431 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-418C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297431 | |||||||
| chr2:176297477 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.89-372C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297477 | |||||||
| chr2:176297543 | C | G | 121 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(118): Show |
135 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.89-306C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297543 | |||||||
| chr2:176297566 | A | C | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-283A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297566 | |||||||
| chr2:176297571 | G | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-278G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297571 | |||||||
| chr2:176297729 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.89-120T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 2/9 | chr2 | 176297729 | |||||||
| chr2:176298076 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.135+181T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298076 | |||||||
| chr2:176298110 | CAT | C | 10 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0090 others(7): Show |
10 | HG00099.hp2 HG00642.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+217_135+218del others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176298110 | ||||||
| chr2:176298116 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.135+221T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298116 | |||||||
| chr2:176298129 | T | A | 1 | a0001c0001t0005g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+234T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298129 | |||||||
| chr2:176298350 | A | G | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(125): Show |
143 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.135+455A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298350 | |||||||
| chr2:176298421 | A | G | 2 | a0001c0001t0002g0272 a0001c0001t0002g0275 |
2 | NA18945.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.135+526A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298421 | |||||||
| chr2:176298500 | T | G | 2 | a0001c0001t0005g0224 a0001c0001t0005g0228 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.135+605T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298500 | |||||||
| chr2:176298533 | G | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+638G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298533 | |||||||
| chr2:176298567 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+672A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298567 | |||||||
| chr2:176298596 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.135+701A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298596 | |||||||
| chr2:176298706 | G | A | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(125): Show |
143 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.135+811G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298706 | |||||||
| chr2:176298891 | G | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+996G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298891 | |||||||
| chr2:176298913 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+1018G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176298913 | |||||||
| chr2:176299082 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.135+1187A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299082 | |||||||
| chr2:176299139 | A | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+1244A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299139 | |||||||
| chr2:176299191 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+1296T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299191 | |||||||
| chr2:176299292 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.135+1397G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299292 | |||||||
| chr2:176299401 | GA | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0289 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+1512delA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176299401 | ||||||
| chr2:176299402 | A | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+1507A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299402 | |||||||
| chr2:176299436 | A | T | 1 | a0002c0002t0003g0039 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.135+1541A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299436 | |||||||
| chr2:176299586 | C | A | 118 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(115): Show |
132 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.135+1691C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299586 | |||||||
| chr2:176299756 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.135+1861A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299756 | |||||||
| chr2:176299942 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.135+2047G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176299942 | |||||||
| chr2:176299949 | T | TGAACTCT others(1496): Show |
1 | a0001c0001t0001g0090 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.135+2071_135+2072i others(1505): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176299949 | ||||||
| chr2:176300133 | TAGAGAGA others(1): Show |
T | 91 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(88): Show |
103 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.135+2246_135+2253d others(10): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176300133 | ||||||
| chr2:176300193 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.135+2298T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176300193 | |||||||
| chr2:176300236 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+2341C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176300236 | |||||||
| chr2:176300556 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.135+2661T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176300556 | |||||||
| chr2:176300647 | A | C | 11 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0001g0174 others(8): Show |
11 | HG00408.hp1 HG01261.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+2752A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176300647 | |||||||
| chr2:176300694 | G | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2799G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176300694 | |||||||
| chr2:176300767 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135+2872A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176300767 | |||||||
| chr2:176301048 | ATGTTTG | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3163_135+3168d others(8): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176301048 | ||||||
| chr2:176301080 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.135+3185A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301080 | |||||||
| chr2:176301309 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG01952.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.135+3414C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301309 | |||||||
| chr2:176301370 | T | G | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3475T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301370 | |||||||
| chr2:176301667 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.135+3772A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301667 | |||||||
| chr2:176301714 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135+3819A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301714 | |||||||
| chr2:176301758 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+3863A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301758 | |||||||
| chr2:176301787 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3892A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301787 | |||||||
| chr2:176301795 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG02280.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+3900A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176301795 | |||||||
| chr2:176302096 | T | C | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+4201T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176302096 | |||||||
| chr2:176302126 | G | GT | 31 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0051 others(28): Show |
33 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.135+4247dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176302126 | ||||||
| chr2:176302131 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.135+4236T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176302131 | |||||||
| chr2:176302145 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.135+4250A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176302145 | |||||||
| chr2:176302459 | T | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+4564T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176302459 | |||||||
| chr2:176302475 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.135+4580C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176302475 | |||||||
| chr2:176302517 | A | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+4622A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176302517 | |||||||
| chr2:176303388 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0140 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+5493T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176303388 | |||||||
| chr2:176303549 | A | G | 84 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(81): Show |
96 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.135+5654A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176303549 | |||||||
| chr2:176303603 | A | T | 3 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0285 |
3 | NA18966.hp2 NA18993.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.135+5708A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176303603 | |||||||
| chr2:176303866 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.135+5971A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176303866 | |||||||
| chr2:176303931 | GT | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0072 a0001c0001t0001g0094 others(3): Show |
7 | HG00639.hp1 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+6039delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176303931 | ||||||
| chr2:176303964 | G | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.135+6069G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176303964 | |||||||
| chr2:176304043 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.135+6148G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304043 | |||||||
| chr2:176304221 | A | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+6326A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304221 | |||||||
| chr2:176304527 | C | A | 100 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(97): Show |
112 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.135+6632C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304527 | |||||||
| chr2:176304537 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0106 a0001c0001t0001g0188 |
4 | HG00639.hp1 HG01099.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+6642T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304537 | |||||||
| chr2:176304649 | A | G | 121 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(118): Show |
135 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.135+6754A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304649 | |||||||
| chr2:176304675 | G | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.135+6780G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304675 | |||||||
| chr2:176304710 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.135+6815T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304710 | |||||||
| chr2:176304838 | G | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+6943G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176304838 | |||||||
| chr2:176305068 | A | G | 8 | a0001c0001t0001g0087 a0001c0001t0001g0138 a0001c0001t0001g0141 others(5): Show |
8 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+7173A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305068 | |||||||
| chr2:176305145 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.135+7250G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305145 | |||||||
| chr2:176305190 | G | A | 80 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(77): Show |
92 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.135+7295G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305190 | |||||||
| chr2:176305440 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(68): Show |
83 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.135+7545C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305440 | |||||||
| chr2:176305699 | T | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+7804T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305699 | |||||||
| chr2:176305747 | C | T | 7 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(4): Show |
7 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+7852C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305747 | |||||||
| chr2:176305874 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.135+7979T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305874 | |||||||
| chr2:176305947 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.135+8052G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176305947 | |||||||
| chr2:176306037 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.135+8142A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306037 | |||||||
| chr2:176306141 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.135+8246A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306141 | |||||||
| chr2:176306308 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.135+8413T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306308 | |||||||
| chr2:176306545 | A | G | 110 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(107): Show |
122 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.135+8650A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306545 | |||||||
| chr2:176306586 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+8691T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306586 | |||||||
| chr2:176306629 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.135+8734T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306629 | |||||||
| chr2:176306698 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.135+8803G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306698 | |||||||
| chr2:176306715 | A | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG02071.hp2 NA18954.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+8820A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306715 | |||||||
| chr2:176306809 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+8914C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306809 | |||||||
| chr2:176306827 | T | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(227): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.135+8932T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306827 | |||||||
| chr2:176306870 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.135+8975T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306870 | |||||||
| chr2:176306890 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135+8995G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306890 | |||||||
| chr2:176306926 | C | T | 3 | a0001c0001t0002g0249 a0001c0001t0002g0261 a0001c0001t0002g0262 |
3 | HG02145.hp1 HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.135+9031C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176306926 | |||||||
| chr2:176307127 | G | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+9232G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307127 | |||||||
| chr2:176307300 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
5 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+9405T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307300 | |||||||
| chr2:176307338 | G | A | 97 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(94): Show |
109 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.135+9443G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307338 | |||||||
| chr2:176307417 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.135+9522T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307417 | |||||||
| chr2:176307567 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+9672C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307567 | |||||||
| chr2:176307715 | T | C | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+9820T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307715 | |||||||
| chr2:176307834 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.135+9939T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307834 | |||||||
| chr2:176307916 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.135+10021C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307916 | |||||||
| chr2:176307938 | C | G | 1 | a0001c0001t0005g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.135+10043C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307938 | |||||||
| chr2:176307976 | G | A | 91 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(88): Show |
103 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.135+10081G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176307976 | |||||||
| chr2:176308111 | A | G | 110 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(107): Show |
122 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.135+10216A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308111 | |||||||
| chr2:176308146 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.135+10251G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308146 | |||||||
| chr2:176308165 | T | G | 1 | a0001c0001t0002g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.135+10270T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308165 | |||||||
| chr2:176308213 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.135+10318G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308213 | |||||||
| chr2:176308299 | T | C | 92 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(89): Show |
104 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.135+10404T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308299 | |||||||
| chr2:176308326 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.135+10431G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308326 | |||||||
| chr2:176308752 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00323.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.135+10857T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308752 | |||||||
| chr2:176308928 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.135+11033T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308928 | |||||||
| chr2:176308981 | G | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+11086G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308981 | |||||||
| chr2:176308999 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+11104G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176308999 | |||||||
| chr2:176309052 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+11157C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309052 | |||||||
| chr2:176309068 | T | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+11173T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309068 | |||||||
| chr2:176309491 | G | T | 6 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG00280.hp1 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+11596G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309491 | |||||||
| chr2:176309506 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+11611A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309506 | |||||||
| chr2:176309516 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.135+11621T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309516 | |||||||
| chr2:176309680 | T | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+11785T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309680 | |||||||
| chr2:176309685 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0164 |
2 | HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.135+11790G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309685 | |||||||
| chr2:176309720 | C | CT | 46 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(43): Show |
50 | HG00558.hp2 HG01081.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.135+11845dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176309720 | ||||||
| chr2:176309720 | CT | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0164 others(10): Show |
13 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.135+11845delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176309720 | ||||||
| chr2:176309748 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.135+11853A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309748 | |||||||
| chr2:176309835 | T | C | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+11940T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309835 | |||||||
| chr2:176309866 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.135+11971A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309866 | |||||||
| chr2:176309941 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.135+12046G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176309941 | |||||||
| chr2:176309994 | T | TA | 11 | a0001c0001t0001g0235 a0001c0001t0002g0033 a0001c0001t0002g0034 others(8): Show |
11 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+12101dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176309994 | ||||||
| chr2:176310082 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+12187C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310082 | |||||||
| chr2:176310181 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0137 |
3 | NA18941.hp1 NA18970.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.135+12286A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310181 | |||||||
| chr2:176310249 | T | C | 127 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(124): Show |
142 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.135+12354T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310249 | |||||||
| chr2:176310272 | T | TCTG | 110 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(107): Show |
122 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.135+12378_135+1238 others(7): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176310272 | ||||||
| chr2:176310310 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.135+12415A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310310 | |||||||
| chr2:176310546 | G | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+12651G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310546 | |||||||
| chr2:176310654 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136-12738C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310654 | |||||||
| chr2:176310694 | A | G | 1 | a0001c0001t0002g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.136-12698A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310694 | |||||||
| chr2:176310934 | T | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-12458T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310934 | |||||||
| chr2:176310978 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-12414C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310978 | |||||||
| chr2:176310979 | A | G | 127 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(124): Show |
142 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.136-12413A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176310979 | |||||||
| chr2:176311380 | T | G | 110 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(107): Show |
122 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.136-12012T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311380 | |||||||
| chr2:176311400 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.136-11992C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311400 | |||||||
| chr2:176311404 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-11988C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311404 | |||||||
| chr2:176311457 | A | C | 1 | a0001c0001t0006g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136-11935A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311457 | |||||||
| chr2:176311467 | A | T | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.136-11925A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311467 | |||||||
| chr2:176311494 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.136-11898A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311494 | |||||||
| chr2:176311518 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-11874G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311518 | |||||||
| chr2:176311538 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-11854T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311538 | |||||||
| chr2:176311555 | C | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(54): Show |
67 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.136-11837C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311555 | |||||||
| chr2:176311621 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.136-11771C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311621 | |||||||
| chr2:176311698 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.136-11694A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311698 | |||||||
| chr2:176311763 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.136-11629A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311763 | |||||||
| chr2:176311850 | C | G | 80 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(77): Show |
92 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.136-11542C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311850 | |||||||
| chr2:176311850 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.136-11542C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311850 | |||||||
| chr2:176311897 | A | G | 2 | a0001c0001t0002g0271 a0001c0001t0002g0287 |
2 | NA18964.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.136-11495A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311897 | |||||||
| chr2:176311901 | G | C | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-11491G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311901 | |||||||
| chr2:176311980 | C | T | 1 | a0001c0001t0004g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136-11412C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176311980 | |||||||
| chr2:176312022 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.136-11370C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312022 | |||||||
| chr2:176312097 | G | A | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0304 |
3 | HG01243.hp2 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.136-11295G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312097 | |||||||
| chr2:176312133 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01071.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.136-11259T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312133 | |||||||
| chr2:176312181 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-11211G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312181 | |||||||
| chr2:176312189 | T | C | 95 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(92): Show |
107 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-11203T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312189 | |||||||
| chr2:176312190 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-11202G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312190 | |||||||
| chr2:176312232 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11160C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312232 | |||||||
| chr2:176312235 | G | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0046 others(74): Show |
79 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.136-11157G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312235 | |||||||
| chr2:176312304 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-11088G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312304 | |||||||
| chr2:176312601 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.136-10791C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312601 | |||||||
| chr2:176312606 | G | C | 1 | a0001c0001t0002g0237 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-10786G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312606 | |||||||
| chr2:176312794 | C | T | 11 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0002c0002t0003g0037 others(8): Show |
11 | HG02040.hp2 HG02083.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-10598C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312794 | |||||||
| chr2:176312823 | A | AT | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-10567dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176312823 | ||||||
| chr2:176312863 | C | CA | 54 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0027 others(51): Show |
58 | HG00741.hp1 HG01081.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.136-10508dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176312863 | ||||||
| chr2:176312863 | CA | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0110 a0001c0001t0001g0124 others(7): Show |
11 | HG00099.hp1 HG01081.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-10508delA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176312863 | ||||||
| chr2:176312938 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.136-10454T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176312938 | |||||||
| chr2:176313030 | T | A | 1 | a0001c0001t0004g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-10362T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313030 | |||||||
| chr2:176313312 | C | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-10080C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313312 | |||||||
| chr2:176313388 | C | CT | 56 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0061 others(53): Show |
59 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.136-9983dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176313388 | ||||||
| chr2:176313388 | C | CTT | 49 | a0001c0001t0001g0106 a0001c0001t0002g0002 a0001c0001t0002g0018 others(46): Show |
59 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.136-9984_136-9983d others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176313388 | ||||||
| chr2:176313388 | C | CTTT | 18 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0290 others(15): Show |
18 | HG01099.hp2 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.136-9985_136-9983d others(5): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176313388 | ||||||
| chr2:176313388 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.136-9995_136-9983d others(15): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176313388 | ||||||
| chr2:176313388 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-10002_136-9983 others(23): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176313388 | ||||||
| chr2:176313388 | CT | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
17 | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.136-9983delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176313388 | ||||||
| chr2:176313432 | T | A | 100 | a0001c0001t0001g0023 a0001c0001t0001g0235 a0001c0001t0001g0290 others(97): Show |
112 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.136-9960T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313432 | |||||||
| chr2:176313479 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.136-9913A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313479 | |||||||
| chr2:176313600 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.136-9792G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313600 | |||||||
| chr2:176313792 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
5 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-9600C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313792 | |||||||
| chr2:176313909 | G | A | 4 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0042 others(1): Show |
4 | HG02040.hp2 NA18747.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-9483G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313909 | |||||||
| chr2:176313998 | A | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-9394A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176313998 | |||||||
| chr2:176314043 | T | G | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-9349T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176314043 | |||||||
| chr2:176314047 | C | CT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
13 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-9335dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176314047 | ||||||
| chr2:176314193 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.136-9199T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176314193 | |||||||
| chr2:176314436 | C | CA | 7 | a0001c0001t0001g0133 a0001c0001t0001g0156 a0001c0001t0001g0180 others(4): Show |
7 | HG02071.hp2 HG02615.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-8943dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176314436 | ||||||
| chr2:176314545 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136-8847T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176314545 | |||||||
| chr2:176314889 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.136-8503C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176314889 | |||||||
| chr2:176315039 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-8353G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176315039 | |||||||
| chr2:176315707 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.136-7685T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176315707 | |||||||
| chr2:176316018 | CA | C | 14 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(11): Show |
16 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-7373delA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316018 | |||||||
| chr2:176316127 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.136-7265A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316127 | |||||||
| chr2:176316128 | A | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-7264A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316128 | |||||||
| chr2:176316170 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-7222T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316170 | |||||||
| chr2:176316199 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136-7193T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316199 | |||||||
| chr2:176316260 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
5 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-7132A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316260 | |||||||
| chr2:176316334 | T | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-7058T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316334 | |||||||
| chr2:176316365 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.136-7027G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316365 | |||||||
| chr2:176316410 | G | T | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6982G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316410 | |||||||
| chr2:176316431 | T | C | 2 | a0001c0001t0002g0284 a0001c0001t0002g0286 |
2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.136-6961T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316431 | |||||||
| chr2:176316482 | G | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-6910G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316482 | |||||||
| chr2:176316515 | C | T | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-6877C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316515 | |||||||
| chr2:176316530 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-6862T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316530 | |||||||
| chr2:176316531 | A | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0072 a0001c0001t0001g0074 others(5): Show |
9 | HG00639.hp1 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-6861A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316531 | |||||||
| chr2:176316936 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.136-6456G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176316936 | |||||||
| chr2:176317029 | T | G | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
13 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-6363T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317029 | |||||||
| chr2:176317032 | C | CT | 16 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(13): Show |
18 | HG01884.hp2 HG02040.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.136-6354dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176317032 | ||||||
| chr2:176317037 | T | TA | 114 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0046 others(111): Show |
126 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.136-6355_136-6354i others(3): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317037 | |||||||
| chr2:176317037 | T | TAA | 7 | a0001c0001t0001g0083 a0001c0001t0001g0108 a0001c0001t0001g0155 others(4): Show |
7 | HG01358.hp2 HG02135.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6355_136-6354i others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317037 | |||||||
| chr2:176317038 | T | A | 135 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0024 others(132): Show |
148 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.136-6354T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317038 | |||||||
| chr2:176317038 | T | TA | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00639.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-6341dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176317038 | ||||||
| chr2:176317038 | T | TAA | 9 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0002g0035 others(6): Show |
9 | HG00280.hp1 HG00558.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-6342_136-6341d others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176317038 | ||||||
| chr2:176317038 | T | TAAA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0292 others(4): Show |
7 | HG02055.hp2 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6343_136-6341d others(5): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176317038 | ||||||
| chr2:176317052 | C | A | 169 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(166): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.136-6340C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317052 | |||||||
| chr2:176317053 | A | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(2): Show |
7 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6339A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317053 | |||||||
| chr2:176317107 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6285C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317107 | |||||||
| chr2:176317151 | T | G | 14 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(11): Show |
16 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-6241T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317151 | |||||||
| chr2:176317314 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.136-6078G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317314 | |||||||
| chr2:176317346 | T | TA | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6044dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176317346 | ||||||
| chr2:176317501 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-5891A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317501 | |||||||
| chr2:176317563 | G | GATA | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-5827_136-5826i others(5): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176317563 | ||||||
| chr2:176317698 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-5694G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317698 | |||||||
| chr2:176317726 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.136-5666A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317726 | |||||||
| chr2:176317924 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.136-5468C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317924 | |||||||
| chr2:176317949 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-5443A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317949 | |||||||
| chr2:176317991 | T | A | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-5401T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317991 | |||||||
| chr2:176317993 | TC | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-5398delC | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176317993 | |||||||
| chr2:176318206 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0159 |
3 | HG00099.hp2 HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.136-5186C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318206 | |||||||
| chr2:176318243 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-5149G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318243 | |||||||
| chr2:176318251 | C | T | 189 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(186): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.136-5141C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318251 | |||||||
| chr2:176318431 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-4961A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318431 | |||||||
| chr2:176318478 | T | C | 1 | a0001c0001t0005g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-4914T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318478 | |||||||
| chr2:176318733 | T | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-4659T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318733 | |||||||
| chr2:176318887 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.136-4505C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318887 | |||||||
| chr2:176318997 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-4395T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176318997 | |||||||
| chr2:176319005 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136-4387C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319005 | |||||||
| chr2:176319149 | T | G | 1 | a0003c0008t0002g0233 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.136-4243T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319149 | |||||||
| chr2:176319358 | G | A | 9 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
10 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-4034G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319358 | |||||||
| chr2:176319395 | AG | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-3994delG | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176319395 | ||||||
| chr2:176319442 | C | CT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0051 others(8): Show |
13 | HG00639.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-3934dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176319442 | ||||||
| chr2:176319442 | CT | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(169): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.136-3934delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176319442 | ||||||
| chr2:176319442 | CTT | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-3935_136-3934d others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176319442 | ||||||
| chr2:176319467 | A | G | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-3925A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319467 | |||||||
| chr2:176319489 | A | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-3903A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319489 | |||||||
| chr2:176319644 | C | T | 170 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(167): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.136-3748C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319644 | |||||||
| chr2:176319692 | C | T | 17 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0242 others(14): Show |
22 | HG00642.hp2 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.136-3700C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319692 | |||||||
| chr2:176319849 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136-3543T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319849 | |||||||
| chr2:176319992 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-3400T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176319992 | |||||||
| chr2:176320181 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-3211A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320181 | |||||||
| chr2:176320212 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-3180C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320212 | |||||||
| chr2:176320247 | C | CA | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-3135dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176320247 | ||||||
| chr2:176320366 | A | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(166): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.136-3026A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320366 | |||||||
| chr2:176320537 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-2855G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320537 | |||||||
| chr2:176320562 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.136-2830G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320562 | |||||||
| chr2:176320583 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-2809G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320583 | |||||||
| chr2:176320695 | CT | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(168): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.136-2680delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176320695 | ||||||
| chr2:176320725 | T | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(179): Show |
196 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.136-2667T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176320725 | |||||||
| chr2:176321145 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.136-2247G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321145 | |||||||
| chr2:176321344 | T | A | 1 | a0001c0001t0006g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.136-2048T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321344 | |||||||
| chr2:176321345 | T | C | 1 | a0001c0001t0006g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.136-2047T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321345 | |||||||
| chr2:176321346 | A | C | 1 | a0001c0001t0006g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.136-2046A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321346 | |||||||
| chr2:176321768 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-1624A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321768 | |||||||
| chr2:176321915 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1477A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321915 | |||||||
| chr2:176321948 | G | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0092 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-1444G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176321948 | |||||||
| chr2:176322281 | A | G | 1 | a0001c0001t0005g0230 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-1111A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322281 | |||||||
| chr2:176322343 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.136-1049A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322343 | |||||||
| chr2:176322351 | GTTAA | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1038_136-1035d others(6): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 176322351 | ||||||
| chr2:176322431 | C | G | 14 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(11): Show |
16 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-961C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322431 | |||||||
| chr2:176322717 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.136-675G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322717 | |||||||
| chr2:176322740 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.136-652T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322740 | |||||||
| chr2:176322775 | G | C | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-617G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322775 | |||||||
| chr2:176322855 | G | A | 181 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(178): Show |
195 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.136-537G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176322855 | |||||||
| chr2:176323013 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-379T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176323013 | |||||||
| chr2:176323225 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-167G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 3/9 | chr2 | 176323225 | |||||||
| chr2:176323860 | CA | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0091 a0001c0001t0001g0127 |
3 | HG02622.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+397delA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176323860 | |||||||
| chr2:176324022 | A | C | 1 | a0001c0001t0002g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.208+558A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324022 | |||||||
| chr2:176324158 | C | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+694C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324158 | |||||||
| chr2:176324203 | G | A | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.208+739G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324203 | |||||||
| chr2:176324398 | A | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+934A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324398 | |||||||
| chr2:176324548 | T | G | 1 | a0001c0001t0001g0110 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.208+1084T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324548 | |||||||
| chr2:176324752 | C | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1288C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324752 | |||||||
| chr2:176324795 | A | C | 1 | a0001c0001t0002g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.208+1331A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176324795 | |||||||
| chr2:176325069 | A | G | 1 | a0001c0001t0005g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+1605A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325069 | |||||||
| chr2:176325111 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.208+1647A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325111 | |||||||
| chr2:176325243 | C | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
5 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-1582C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325243 | |||||||
| chr2:176325295 | C | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-1530C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325295 | |||||||
| chr2:176325578 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.209-1247A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325578 | |||||||
| chr2:176325723 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0197 |
2 | HG02074.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.209-1102C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325723 | |||||||
| chr2:176325740 | G | A | 177 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(174): Show |
191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.209-1085G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325740 | |||||||
| chr2:176325768 | A | T | 2 | a0001c0001t0002g0269 a0001c0001t0002g0277 |
2 | NA18948.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.209-1057A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325768 | |||||||
| chr2:176325821 | A | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0192 |
3 | HG01934.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.209-1004A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325821 | |||||||
| chr2:176325841 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0127 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.209-984A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325841 | |||||||
| chr2:176325952 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.209-873C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325952 | |||||||
| chr2:176325954 | C | A | 6 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0243 others(3): Show |
8 | NA18939.hp2 NA18980.hp1 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-871C>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176325954 | |||||||
| chr2:176325995 | GA | G | 168 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(165): Show |
182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.209-828delA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 176325995 | ||||||
| chr2:176326522 | T | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(53): Show |
66 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-303T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 4/9 | chr2 | 176326522 | |||||||
| chr2:176326947 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.285+46C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176326947 | |||||||
| chr2:176326978 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.285+77T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176326978 | |||||||
| chr2:176327091 | CTA | C | 148 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0046 others(145): Show |
162 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.285+192_285+193del others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 176327091 | ||||||
| chr2:176327138 | T | A | 204 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(201): Show |
221 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.285+237T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327138 | |||||||
| chr2:176327424 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+523G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327424 | |||||||
| chr2:176327481 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.285+580C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327481 | |||||||
| chr2:176327542 | A | C | 1 | a0001c0001t0001g0180 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.285+641A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327542 | |||||||
| chr2:176327563 | A | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+662A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327563 | |||||||
| chr2:176327576 | A | AT | 140 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0025 others(137): Show |
153 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.285+685dupT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 176327576 | ||||||
| chr2:176327593 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.285+692C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327593 | |||||||
| chr2:176327640 | T | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-653T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327640 | |||||||
| chr2:176327683 | G | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0046 others(131): Show |
146 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.286-610G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327683 | |||||||
| chr2:176327712 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.286-581C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327712 | |||||||
| chr2:176327937 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.286-356T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176327937 | |||||||
| chr2:176328206 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.286-87C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 5/9 | chr2 | 176328206 | |||||||
| chr2:176328410 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.378+25G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 6/9 | chr2 | 176328410 | |||||||
| chr2:176328660 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.379-214C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 6/9 | chr2 | 176328660 | |||||||
| chr2:176328711 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(54): Show |
67 | HG00408.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.379-163G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 6/9 | chr2 | 176328711 | |||||||
| chr2:176328976 | C | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.417+64C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 7/9 | chr2 | 176328976 | |||||||
| chr2:176329027 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.417+115T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 7/9 | chr2 | 176329027 | |||||||
| chr2:176329180 | A | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-121A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 7/9 | chr2 | 176329180 | |||||||
| chr2:176329248 | C | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.418-53C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 7/9 | chr2 | 176329248 | |||||||
| chr2:176329793 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG02615.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.543+367A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176329793 | |||||||
| chr2:176329878 | T | C | 5 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+452T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176329878 | |||||||
| chr2:176329882 | C | CGTCT | 196 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(193): Show |
211 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.543+465_543+468dup others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 176329882 | ||||||
| chr2:176329882 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+456C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176329882 | |||||||
| chr2:176329895 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+469A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176329895 | |||||||
| chr2:176329903 | GTCTA | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+481_543+484del others(4): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 176329903 | ||||||
| chr2:176330044 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG02280.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-540C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330044 | |||||||
| chr2:176330053 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-531G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330053 | |||||||
| chr2:176330067 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.544-517A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330067 | |||||||
| chr2:176330135 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.544-449A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330135 | |||||||
| chr2:176330155 | A | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(202): Show |
222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.544-429A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330155 | |||||||
| chr2:176330257 | T | TTA | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-324_544-323dup others(2): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 176330257 | ||||||
| chr2:176330346 | A | ACTTATAT others(24): Show |
9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-189_544-159dup others(31): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 176330346 | ||||||
| chr2:176330369 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544-215T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330369 | |||||||
| chr2:176330382 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.544-202T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330382 | |||||||
| chr2:176330457 | ATATAT | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-122_544-118del others(5): Show |
MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 176330457 | ||||||
| chr2:176330482 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.544-102T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 8/9 | chr2 | 176330482 | |||||||
| chr2:176330743 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.620+83C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176330743 | |||||||
| chr2:176330812 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.620+152C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176330812 | |||||||
| chr2:176330848 | A | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
17 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.620+188A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176330848 | |||||||
| chr2:176330883 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.620+223G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176330883 | |||||||
| chr2:176330957 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.620+297C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176330957 | |||||||
| chr2:176331088 | T | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+428T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331088 | |||||||
| chr2:176331273 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+613A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331273 | |||||||
| chr2:176331386 | G | A | 205 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(202): Show |
222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.620+726G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331386 | |||||||
| chr2:176331629 | G | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0088 others(3): Show |
8 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.620+969G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331629 | |||||||
| chr2:176331653 | A | G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.620+993A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331653 | |||||||
| chr2:176331675 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.620+1015G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331675 | |||||||
| chr2:176331702 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+1042A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331702 | |||||||
| chr2:176331760 | A | T | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+1100A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331760 | |||||||
| chr2:176331785 | A | G | 184 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(181): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.620+1125A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331785 | |||||||
| chr2:176331817 | G | C | 175 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(172): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.620+1157G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331817 | |||||||
| chr2:176331960 | C | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(2): Show |
7 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+1300C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176331960 | |||||||
| chr2:176332331 | G | A | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+1671G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176332331 | |||||||
| chr2:176332355 | A | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+1695A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176332355 | |||||||
| chr2:176332386 | G | T | 7 | a0001c0001t0001g0235 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+1726G>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176332386 | |||||||
| chr2:176332436 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+1776T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176332436 | |||||||
| chr2:176332747 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.620+2087G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176332747 | |||||||
| chr2:176332998 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.620+2338T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176332998 | |||||||
| chr2:176333005 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.620+2345G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333005 | |||||||
| chr2:176333149 | A | G | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01952.hp1 HG02523.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.620+2489A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333149 | |||||||
| chr2:176333163 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.620+2503A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333163 | |||||||
| chr2:176333197 | G | C | 2 | a0001c0001t0002g0263 a0001c0001t0002g0266 |
2 | HG00741.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.620+2537G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333197 | |||||||
| chr2:176333382 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0160 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.620+2722C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333382 | |||||||
| chr2:176333384 | T | C | 2 | a0002c0002t0003g0037 a0002c0002t0003g0038 |
2 | NA18954.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.620+2724T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333384 | |||||||
| chr2:176333425 | T | C | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+2765T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333425 | |||||||
| chr2:176333521 | C | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(189): Show |
208 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.620+2861C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333521 | |||||||
| chr2:176333607 | AT | A | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.620+2948delT | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333607 | |||||||
| chr2:176333639 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.620+2979C>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333639 | |||||||
| chr2:176333749 | T | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0269 a0001c0001t0002g0277 others(1): Show |
5 | HG02040.hp1 NA18941.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.620+3089T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333749 | |||||||
| chr2:176333764 | T | G | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.620+3104T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333764 | |||||||
| chr2:176333817 | T | G | 193 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(190): Show |
208 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.620+3157T>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333817 | |||||||
| chr2:176333818 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.620+3158G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333818 | |||||||
| chr2:176333820 | T | A | 193 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(190): Show |
208 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.620+3160T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333820 | |||||||
| chr2:176333989 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.620+3329A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176333989 | |||||||
| chr2:176334062 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0054 a0001c0001t0004g0055 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+3402C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334062 | |||||||
| chr2:176334118 | G | A | 187 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(184): Show |
202 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.621-3375G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334118 | |||||||
| chr2:176334174 | T | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0218 others(4): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-3319T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334174 | |||||||
| chr2:176334395 | T | C | 9 | a0002c0002t0003g0037 a0002c0002t0003g0038 a0002c0002t0003g0039 others(6): Show |
9 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-3098T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334395 | |||||||
| chr2:176334397 | A | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(202): Show |
222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.621-3096A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334397 | |||||||
| chr2:176334686 | A | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(202): Show |
222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.621-2807A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334686 | |||||||
| chr2:176334691 | T | C | 170 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(167): Show |
184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.621-2802T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176334691 | |||||||
| chr2:176335045 | C | CA | 177 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(174): Show |
191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.621-2438dupA | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 176335045 | ||||||
| chr2:176335051 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02922.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.621-2442A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335051 | |||||||
| chr2:176335257 | T | C | 1 | a0001c0001t0002g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621-2236T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335257 | |||||||
| chr2:176335280 | A | G | 1 | a0001c0001t0001g0007 | 2 | HG01433.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.621-2213A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335280 | |||||||
| chr2:176335290 | A | G | 4 | a0001c0001t0002g0241 a0001c0001t0002g0248 a0001c0001t0002g0250 others(1): Show |
4 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-2203A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335290 | |||||||
| chr2:176335673 | G | A | 8 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0172 others(5): Show |
8 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-1820G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335673 | |||||||
| chr2:176335862 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.621-1631A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335862 | |||||||
| chr2:176335928 | G | C | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-1565G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176335928 | |||||||
| chr2:176336162 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.621-1331G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176336162 | |||||||
| chr2:176336386 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.621-1107G>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176336386 | |||||||
| chr2:176336525 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0295 a0001c0001t0001g0296 |
4 | HG02055.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-968A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176336525 | |||||||
| chr2:176337020 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.621-473A>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337020 | |||||||
| chr2:176337024 | A | G | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
5 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.621-469A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337024 | |||||||
| chr2:176337046 | T | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
7 | HG02055.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.621-447T>A | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337046 | |||||||
| chr2:176337081 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.621-412A>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337081 | |||||||
| chr2:176337342 | T | C | 176 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(173): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.621-151T>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337342 | |||||||
| chr2:176337370 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
7 | HG02055.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.621-123A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337370 | |||||||
| chr2:176337381 | G | C | 1 | a0001c0001t0001g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.621-112G>C | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337381 | |||||||
| chr2:176337387 | A | G | 185 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0023 others(182): Show |
199 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.621-106A>G | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337387 | |||||||
| chr2:176337465 | C | T | 1 | a0001c0001t0001g0010 | 2 | NA18961.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.621-28C>T | MTX2 | ENSG00000128654.14 | transcript | ENST00000249442.11 | protein_coding | 9/9 | chr2 | 176337465 |