Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29767 |
| ensemblid | ENSG00000128872.10 |
| hgncid | 11872 |
| symbol | TMOD2 |
| name | tropomodulin 2 |
| refseq_nuc | NM_014548.4 |
| refseq_prot | NP_055363.1 |
| ensembl_nuc | ENST00000249700.9 |
| ensembl_prot | ENSP00000249700.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 51751597 |
| end | 51816363 |
| strand | + |
| ver | v1.2 |
| region | chr15:51751597-51816363 |
| region5000 | chr15:51746597-51821363 |
| regionname0 | TMOD2_chr15_51751597_51816363 |
| regionname5000 | TMOD2_chr15_51746597_51821363 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 367 | 90 | 67 | 162 | 10 | 36 | 138 | TMOD2_chr15_51746597_51821363 | TMOD2 | MALPF others(346): Show |
chr15 | 51746597 | 51821363 |
| a0002 | 0/0 | 351 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | MALPF others(346): Show |
chr15 | 51746597 | 51821363 |
| a0003 | 0/0 | 351 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | MALPF others(346): Show |
chr15 | 51746597 | 51821363 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1053 | 366 | 90 | 67 | 161 | 10 | 36 | TMOD2_chr15_51746597_51821363 | TMOD2 | ATGGC others(1048): Show |
chr15 | 51746597 | 51821363 | ||
| a0001c0004 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | ATGGC others(1048): Show |
chr15 | 51746597 | 51821363 | ||
| a0002c0002 | 0/0 | 1053 | 5 | 0 | 5 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | ATGGC others(1048): Show |
chr15 | 51746597 | 51821363 | ||
| a0003c0003 | 0/0 | 1053 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | ATGGC others(1048): Show |
chr15 | 51746597 | 51821363 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9150 | 81 | 20 | 8 | 46 | 0 | 7 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0002 | 0/0 | 9151 | 61 | 12 | 8 | 37 | 2 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0003 | 1/0 | 9150 | 29 | 2 | 16 | 0 | 3 | 7 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0004 | 0/1 | 9150 | 20 | 2 | 8 | 1 | 3 | 5 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0005 | 0/0 | 9151 | 25 | 0 | 9 | 15 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0006 | 0/0 | 9151 | 19 | 0 | 1 | 18 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0007 | 0/0 | 9150 | 19 | 18 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0008 | 0/0 | 9150 | 11 | 0 | 0 | 5 | 0 | 6 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0009 | 0/0 | 9151 | 9 | 0 | 0 | 7 | 1 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0010 | 0/0 | 9150 | 8 | 7 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0011 | 0/0 | 9150 | 7 | 0 | 0 | 7 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0012 | 0/0 | 9151 | 7 | 7 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0013 | 0/0 | 9151 | 5 | 0 | 0 | 4 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0014 | 0/0 | 9150 | 4 | 0 | 0 | 4 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0015 | 0/0 | 9150 | 4 | 0 | 3 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0016 | 0/0 | 9151 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0017 | 0/0 | 9151 | 3 | 1 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0018 | 0/0 | 9150 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0019 | 0/0 | 9150 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0020 | 0/0 | 9151 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0021 | 0/0 | 9151 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0022 | 0/0 | 9150 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0023 | 0/0 | 9151 | 2 | 0 | 0 | 1 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0024 | 0/0 | 9138 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9133): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0025 | 0/0 | 9150 | 2 | 0 | 1 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0026 | 0/0 | 9150 | 2 | 0 | 1 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0027 | 0/0 | 9150 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0028 | 0/0 | 9151 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0029 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0030 | 0/0 | 9150 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0031 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0032 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0033 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0034 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0035 | 0/0 | 9151 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0036 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0037 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0038 | 0/0 | 9151 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0039 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0040 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0041 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0042 | 0/0 | 9149 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9144): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0043 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0044 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0045 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0046 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0047 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0048 | 0/0 | 9150 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0049 | 0/0 | 9149 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9144): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0050 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0051 | 0/0 | 9149 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9144): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0052 | 0/0 | 9150 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0053 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0054 | 0/0 | 9151 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0055 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0001t0056 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0001c0004t0002 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9146): Show |
chr15 | 51746597 | 51821363 |
| a0002c0002t0004 | 0/0 | 9150 | 5 | 0 | 5 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| a0003c0003t0003 | 0/0 | 9150 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | GTTGA others(9145): Show |
chr15 | 51746597 | 51821363 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0002 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0008g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0011g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0013g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0014g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0014g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0014g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0014g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0015g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0015g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0015g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0015g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0016g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0016g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0017g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0018g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0018g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0019g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0019g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0019g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0020g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0020g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0021g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0021g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0022g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0022g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0023g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0023g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0024g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0025g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0025g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0026g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0026g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0027g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0028g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0029g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0030g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0031g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0032g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0033g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0034g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0035g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0036g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0037g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0038g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0039g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0040g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0041g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0042g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0043g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0044g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0045g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0046g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0047g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0048g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0049g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0050g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0051g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0052g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0053g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0054g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0055g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0001t0056g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0001c0004t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0002c0002t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0002c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| a0003c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0076 | EUR | GBR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0157 | EUR | GBR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0096 | EUR | FIN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0225 | EUR | FIN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00408 | hp1 | a0001 | c0001 | t0011 | g0328 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00609 | hp2 | a0001 | c0001 | t0021 | g0095 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG00741 | hp2 | a0001 | c0001 | t0035 | g0023 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0232 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0186 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01167 | hp1 | a0001 | c0001 | t0017 | g0005 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0071 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01169 | hp2 | a0001 | c0001 | t0017 | g0005 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0220 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01256 | hp2 | a0001 | c0001 | t0020 | g0062 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01257 | hp2 | a0001 | c0001 | t0027 | g0019 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01258 | hp1 | a0001 | c0001 | t0020 | g0113 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01258 | hp2 | a0001 | c0001 | t0027 | g0019 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01358 | hp2 | a0001 | c0001 | t0026 | g0246 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0180 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01496 | hp2 | a0001 | c0001 | t0028 | g0080 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0054 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01515 | hp2 | a0001 | c0001 | t0015 | g0210 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01884 | hp1 | a0001 | c0001 | t0034 | g0118 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01928 | hp2 | a0002 | c0002 | t0004 | g0007 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01943 | hp1 | a0001 | c0001 | t0052 | g0191 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01943 | hp2 | a0002 | c0002 | t0004 | g0068 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0172 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01952 | hp2 | a0002 | c0002 | t0004 | g0007 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01978 | hp1 | a0001 | c0001 | t0054 | g0187 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0189 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0211 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01993 | hp1 | a0002 | c0002 | t0004 | g0065 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0173 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02027 | hp2 | a0001 | c0001 | t0021 | g0052 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0256 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0053 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0137 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CDX | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0217 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02273 | hp1 | a0002 | c0002 | t0004 | g0064 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02273 | hp2 | a0001 | c0001 | t0025 | g0345 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0112 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0190 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0132 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02602 | hp2 | a0001 | c0001 | t0048 | g0264 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0117 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0196 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0216 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0114 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0115 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02895 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0146 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0230 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02970 | hp2 | a0001 | c0001 | t0018 | g0258 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0259 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03098 | hp2 | a0001 | c0001 | t0019 | g0201 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03130 | hp2 | a0001 | c0001 | t0049 | g0269 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0081 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0202 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0138 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03486 | hp2 | a0001 | c0001 | t0053 | g0169 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0020 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03490 | hp2 | a0001 | c0001 | t0051 | g0313 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03491 | hp2 | a0001 | c0001 | t0026 | g0245 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03492 | hp2 | a0003 | c0003 | t0003 | g0020 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0257 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0129 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0139 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0268 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0253 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03704 | hp2 | a0001 | c0001 | t0030 | g0063 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0078 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0348 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04115 | hp1 | a0001 | c0001 | t0013 | g0144 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0271 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04199 | hp2 | a0001 | c0001 | t0023 | g0244 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04204 | hp1 | a0001 | c0001 | t0038 | g0048 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0261 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0208 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18747 | hp1 | a0001 | c0001 | t0013 | g0143 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18906 | hp1 | a0001 | c0001 | t0037 | g0028 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18939 | hp1 | a0001 | c0001 | t0014 | g0280 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18940 | hp1 | a0001 | c0001 | t0011 | g0281 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18945 | hp2 | a0001 | c0001 | t0014 | g0317 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18946 | hp1 | a0001 | c0001 | t0029 | g0031 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18946 | hp2 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18954 | hp2 | a0001 | c0001 | t0047 | g0275 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18957 | hp1 | a0001 | c0001 | t0009 | g0159 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18960 | hp1 | a0001 | c0001 | t0045 | g0160 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18960 | hp2 | a0001 | c0001 | t0011 | g0296 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0297 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18964 | hp2 | a0001 | c0001 | t0011 | g0279 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18967 | hp2 | a0001 | c0001 | t0014 | g0321 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18971 | hp1 | a0001 | c0001 | t0013 | g0140 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18971 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18977 | hp2 | a0001 | c0001 | t0013 | g0142 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18978 | hp1 | a0001 | c0001 | t0009 | g0165 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18979 | hp2 | a0001 | c0001 | t0050 | g0293 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18980 | hp2 | a0001 | c0001 | t0025 | g0346 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18982 | hp2 | a0001 | c0001 | t0009 | g0163 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18987 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18992 | hp1 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18992 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18993 | hp1 | a0001 | c0001 | t0011 | g0298 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18993 | hp2 | a0001 | c0001 | t0044 | g0161 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0162 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18999 | hp1 | a0001 | c0001 | t0032 | g0091 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19004 | hp1 | a0001 | c0001 | t0009 | g0164 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19007 | hp1 | a0001 | c0001 | t0023 | g0327 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19007 | hp2 | a0001 | c0001 | t0056 | g0141 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19010 | hp1 | a0001 | c0001 | t0055 | g0171 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19011 | hp1 | a0001 | c0001 | t0046 | g0263 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19012 | hp1 | a0001 | c0001 | t0041 | g0038 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19012 | hp2 | a0001 | c0001 | t0014 | g0307 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19030 | hp1 | a0001 | c0001 | t0022 | g0270 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0199 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19056 | hp1 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19058 | hp1 | a0001 | c0001 | t0039 | g0101 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19058 | hp2 | a0001 | c0001 | t0011 | g0299 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19078 | hp2 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19081 | hp2 | a0001 | c0001 | t0040 | g0040 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19086 | hp2 | a0001 | c0001 | t0043 | g0283 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0133 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA19240 | hp2 | a0001 | c0001 | t0042 | g0111 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ASW | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ASW | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | GIH | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0158 | SAS | GIH | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01123 | hp1 | a0001 | c0001 | t0015 | g0209 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02486 | hp1 | a0001 | c0001 | t0019 | g0197 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02559 | hp1 | a0001 | c0001 | t0036 | g0110 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0255 | AFR | USA | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA20300 | hp2 | a0001 | c0001 | t0033 | g0003 | AFR | USA | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0134 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0077 | REF | REF | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0156 | REF | REF | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51766485 | T | C | 1 | a0003 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.44T>C | p.Ile15Thr | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/10 | 229/9150 | 44/1056 | 15/351 | chr15 | 51766485 | |||
| chr15:51768322 | C | G | 1 | a0002 | 5 | HG01928.hp2 HG01943.hp2 HG01952.hp2 others(2): Show |
missense_variant | MODERATE | c.187C>G | p.Pro63Ala | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/10 | 372/9150 | 187/1056 | 63/351 | chr15 | 51768322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51776942 | A | T | 1 | a0001c0004 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.417A>T | p.Gly139Gly | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/10 | 602/9150 | 417/1056 | 139/351 | chr15 | 51776942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51751680 | G | A | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(20): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
5_prime_UTR_variant | MODIFIER | c.-102G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/10 | 14762 | chr15 | 51751680 | ||||||
| chr15:51766439 | G | A | 1 | a0001c0001t0043 | 1 | NA19086.hp2 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/10 | 3 | chr15 | 51766439 | ||||||
| chr15:51808707 | G | A | 3 | a0001c0001t0009 a0001c0001t0044 a0001c0001t0045 |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*253G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 253 | chr15 | 51808707 | ||||||
| chr15:51808738 | T | C | 1 | a0001c0001t0022 | 2 | NA19030.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*284T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 284 | chr15 | 51808738 | ||||||
| chr15:51809148 | T | G | 1 | a0001c0001t0014 | 4 | NA18939.hp1 NA18945.hp2 NA18967.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*694T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 694 | chr15 | 51809148 | ||||||
| chr15:51809176 | C | A | 1 | a0001c0001t0028 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 722 | chr15 | 51809176 | ||||||
| chr15:51809188 | T | C | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(22): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*734T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 734 | chr15 | 51809188 | ||||||
| chr15:51809397 | T | A | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*943T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 943 | chr15 | 51809397 | ||||||
| chr15:51809596 | A | T | 2 | a0001c0001t0040 a0001c0001t0041 |
2 | NA19012.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1142A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1142 | chr15 | 51809596 | ||||||
| chr15:51809728 | TCCTTTCT others(6): Show |
T | 1 | a0001c0001t0024 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1282_*1294delCCCC others(9): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1282 | INFO_REALIGN_3_PRIME | chr15 | 51809728 | |||||
| chr15:51809832 | C | T | 1 | a0001c0001t0026 | 2 | HG01358.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1378C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1378 | chr15 | 51809832 | ||||||
| chr15:51809876 | T | A | 1 | a0001c0001t0029 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1422T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1422 | chr15 | 51809876 | ||||||
| chr15:51809957 | T | C | 1 | a0001c0001t0019 | 3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1503T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1503 | chr15 | 51809957 | ||||||
| chr15:51810059 | C | A | 3 | a0001c0001t0009 a0001c0001t0044 a0001c0001t0045 |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1605C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1605 | chr15 | 51810059 | ||||||
| chr15:51810133 | G | GT | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1682dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1683 | INFO_REALIGN_3_PRIME | chr15 | 51810133 | |||||
| chr15:51810223 | T | C | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1769 | chr15 | 51810223 | ||||||
| chr15:51810434 | G | A | 1 | a0001c0001t0012 | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1980G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1980 | chr15 | 51810434 | ||||||
| chr15:51810485 | A | G | 1 | a0001c0001t0039 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2031A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2031 | chr15 | 51810485 | ||||||
| chr15:51810533 | A | G | 1 | a0001c0001t0051 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2079 | chr15 | 51810533 | ||||||
| chr15:51810550 | C | T | 1 | a0001c0001t0024 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2096C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2096 | chr15 | 51810550 | ||||||
| chr15:51810556 | C | G | 1 | a0001c0001t0050 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2102C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2102 | chr15 | 51810556 | ||||||
| chr15:51810567 | G | C | 2 | a0001c0001t0016 a0001c0001t0024 |
5 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2113G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2113 | chr15 | 51810567 | ||||||
| chr15:51810635 | T | G | 14 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(11): Show |
118 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2181T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2181 | chr15 | 51810635 | ||||||
| chr15:51810750 | CT | C | 8 | a0001c0001t0004 a0001c0001t0030 a0001c0001t0040 others(5): Show |
30 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2313delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2313 | INFO_REALIGN_3_PRIME | chr15 | 51810750 | |||||
| chr15:51810772 | C | G | 1 | a0001c0001t0012 | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2318C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2318 | chr15 | 51810772 | ||||||
| chr15:51810842 | G | A | 1 | a0001c0001t0027 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2388G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2388 | chr15 | 51810842 | ||||||
| chr15:51810896 | G | A | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*2442G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2442 | chr15 | 51810896 | ||||||
| chr15:51810940 | T | C | 5 | a0001c0001t0005 a0001c0001t0052 a0001c0001t0053 others(2): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2486T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2486 | chr15 | 51810940 | ||||||
| chr15:51810984 | G | A | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG02273.hp2 NA18980.hp2 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2530G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2530 | chr15 | 51810984 | ||||||
| chr15:51811224 | G | A | 1 | a0001c0001t0053 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2770G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2770 | chr15 | 51811224 | ||||||
| chr15:51811323 | G | C | 4 | a0001c0001t0005 a0001c0001t0052 a0001c0001t0054 others(1): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2869G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2869 | chr15 | 51811323 | ||||||
| chr15:51811622 | C | A | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(32): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*3168C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3168 | chr15 | 51811622 | ||||||
| chr15:51811662 | C | T | 3 | a0001c0001t0005 a0001c0001t0052 a0001c0001t0054 |
27 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3208C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3208 | chr15 | 51811662 | ||||||
| chr15:51811860 | G | A | 1 | a0001c0001t0031 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3406G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3406 | chr15 | 51811860 | ||||||
| chr15:51812103 | C | G | 1 | a0001c0001t0029 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3649C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3649 | chr15 | 51812103 | ||||||
| chr15:51812463 | A | C | 1 | a0001c0001t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4009A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4009 | chr15 | 51812463 | ||||||
| chr15:51813042 | A | G | 1 | a0001c0001t0011 | 7 | HG00408.hp1 NA18940.hp1 NA18960.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4588A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4588 | chr15 | 51813042 | ||||||
| chr15:51813052 | G | T | 1 | a0001c0001t0054 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4598G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4598 | chr15 | 51813052 | ||||||
| chr15:51813085 | A | C | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(47): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*4631A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4631 | chr15 | 51813085 | ||||||
| chr15:51813238 | C | T | 1 | a0001c0001t0018 | 3 | HG02970.hp2 HG03041.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4784C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4784 | chr15 | 51813238 | ||||||
| chr15:51813419 | A | G | 7 | a0001c0001t0006 a0001c0001t0029 a0001c0001t0036 others(4): Show |
25 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4965A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4965 | chr15 | 51813419 | ||||||
| chr15:51813466 | T | C | 1 | a0001c0001t0047 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5012T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5012 | chr15 | 51813466 | ||||||
| chr15:51813515 | G | A | 1 | a0001c0001t0032 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5061G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5061 | chr15 | 51813515 | ||||||
| chr15:51813558 | C | A | 1 | a0001c0001t0040 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5104C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5104 | chr15 | 51813558 | ||||||
| chr15:51813688 | G | T | 1 | a0001c0001t0017 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5234G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5234 | chr15 | 51813688 | ||||||
| chr15:51813804 | G | A | 1 | a0001c0001t0033 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5350G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5350 | chr15 | 51813804 | ||||||
| chr15:51813817 | A | G | 1 | a0001c0001t0021 | 2 | HG00609.hp2 HG02027.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5363A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5363 | chr15 | 51813817 | ||||||
| chr15:51813832 | C | T | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5378C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5378 | chr15 | 51813832 | ||||||
| chr15:51813995 | A | T | 1 | a0001c0001t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5541A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5541 | chr15 | 51813995 | ||||||
| chr15:51814104 | G | A | 33 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(30): Show |
184 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*5650G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5650 | chr15 | 51814104 | ||||||
| chr15:51814172 | G | C | 1 | a0001c0001t0020 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5718G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5718 | chr15 | 51814172 | ||||||
| chr15:51814287 | C | T | 1 | a0001c0001t0034 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5833C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5833 | chr15 | 51814287 | ||||||
| chr15:51814436 | T | G | 1 | a0001c0001t0032 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5982T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5982 | chr15 | 51814436 | ||||||
| chr15:51814498 | T | G | 1 | a0001c0001t0016 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6044T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6044 | chr15 | 51814498 | ||||||
| chr15:51814560 | G | A | 1 | a0001c0001t0044 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6106G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6106 | chr15 | 51814560 | ||||||
| chr15:51814792 | G | A | 2 | a0001c0001t0013 a0001c0001t0056 |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6338G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6338 | chr15 | 51814792 | ||||||
| chr15:51814857 | A | G | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0020 others(13): Show |
101 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*6403A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6403 | chr15 | 51814857 | ||||||
| chr15:51814864 | G | A | 1 | a0001c0001t0015 | 4 | HG01081.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6410G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6410 | chr15 | 51814864 | ||||||
| chr15:51814882 | C | T | 1 | a0001c0001t0045 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6428C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6428 | chr15 | 51814882 | ||||||
| chr15:51814926 | G | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(52): Show |
336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*6472G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6472 | chr15 | 51814926 | ||||||
| chr15:51814940 | G | A | 1 | a0001c0001t0013 | 5 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6486G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6486 | chr15 | 51814940 | ||||||
| chr15:51815051 | C | T | 1 | a0001c0001t0048 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6597C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6597 | chr15 | 51815051 | ||||||
| chr15:51815089 | C | G | 1 | a0001c0001t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6635C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6635 | chr15 | 51815089 | ||||||
| chr15:51815396 | T | G | 1 | a0001c0001t0012 | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6942T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6942 | chr15 | 51815396 | ||||||
| chr15:51815501 | C | T | 1 | a0001c0001t0042 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7047C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 7047 | chr15 | 51815501 | ||||||
| chr15:51815534 | C | T | 5 | a0001c0001t0006 a0001c0001t0029 a0001c0001t0038 others(2): Show |
23 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7080C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 7080 | chr15 | 51815534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51751866 | G | A | 1 | a0001c0001t0012g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-70+154G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51751866 | |||||||
| chr15:51752061 | C | T | 158 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0001t0001g0248 others(155): Show |
165 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.-70+349C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752061 | |||||||
| chr15:51752118 | G | T | 1 | a0001c0001t0008g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-70+406G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752118 | |||||||
| chr15:51752171 | G | A | 1 | a0001c0001t0017g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-70+459G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752171 | |||||||
| chr15:51752429 | C | T | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-70+717C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752429 | |||||||
| chr15:51752490 | A | G | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-70+778A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752490 | |||||||
| chr15:51752581 | C | T | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-70+869C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752581 | |||||||
| chr15:51752737 | A | C | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-70+1025A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752737 | |||||||
| chr15:51752821 | A | T | 3 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | HG02074.hp1 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-70+1109A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752821 | |||||||
| chr15:51752824 | G | A | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+1112G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752824 | |||||||
| chr15:51752905 | A | G | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.-70+1193A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752905 | |||||||
| chr15:51752918 | G | A | 52 | a0001c0001t0003g0004 a0001c0001t0003g0203 a0001c0001t0003g0204 others(49): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-70+1206G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752918 | |||||||
| chr15:51753083 | G | A | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-70+1371G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753083 | |||||||
| chr15:51753105 | G | A | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70+1393G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753105 | |||||||
| chr15:51753153 | T | A | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-70+1441T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753153 | |||||||
| chr15:51753171 | G | A | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-70+1459G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753171 | |||||||
| chr15:51753190 | A | G | 1 | a0001c0001t0005g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-70+1478A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753190 | |||||||
| chr15:51753445 | A | G | 2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | NA18943.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-70+1733A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753445 | |||||||
| chr15:51753451 | C | T | 51 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(48): Show |
55 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.-70+1739C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753451 | |||||||
| chr15:51753552 | A | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+1840A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753552 | |||||||
| chr15:51753605 | G | T | 1 | a0001c0001t0008g0348 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-70+1893G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753605 | |||||||
| chr15:51753606 | C | T | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-70+1894C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753606 | |||||||
| chr15:51753705 | A | G | 1 | a0001c0001t0005g0194 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-70+1993A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753705 | |||||||
| chr15:51753776 | TA | T | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+2065delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753776 | |||||||
| chr15:51753831 | T | C | 1 | a0001c0001t0035g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-70+2119T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753831 | |||||||
| chr15:51753959 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(118): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-70+2247G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753959 | |||||||
| chr15:51754012 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+2300C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754012 | |||||||
| chr15:51754052 | G | T | 77 | a0001c0001t0001g0021 a0001c0001t0001g0272 a0001c0001t0001g0273 others(74): Show |
78 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-70+2340G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754052 | |||||||
| chr15:51754162 | T | C | 337 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0001t0001g0248 others(334): Show |
359 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.-70+2450T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754162 | |||||||
| chr15:51754168 | C | T | 2 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-70+2456C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754168 | |||||||
| chr15:51754298 | G | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+2586G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754298 | |||||||
| chr15:51754473 | C | T | 50 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(47): Show |
54 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.-70+2761C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754473 | |||||||
| chr15:51754516 | A | G | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+2804A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754516 | |||||||
| chr15:51754660 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-70+2948A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754660 | |||||||
| chr15:51754661 | C | A | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+2949C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754661 | |||||||
| chr15:51754706 | A | T | 1 | a0001c0001t0008g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-70+2994A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754706 | |||||||
| chr15:51754875 | A | G | 1 | a0001c0001t0006g0128 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-70+3163A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754875 | |||||||
| chr15:51754956 | G | A | 1 | a0001c0001t0037g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-70+3244G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754956 | |||||||
| chr15:51755042 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-70+3330T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755042 | |||||||
| chr15:51755080 | T | A | 1 | a0001c0001t0023g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-70+3368T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755080 | |||||||
| chr15:51755233 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-70+3521A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755233 | |||||||
| chr15:51755240 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+3528G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755240 | |||||||
| chr15:51755609 | G | T | 2 | a0001c0001t0009g0163 a0001c0001t0009g0164 |
2 | NA18982.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-70+3897G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755609 | |||||||
| chr15:51755782 | A | G | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-70+4070A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755782 | |||||||
| chr15:51755895 | T | C | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0047g0275 |
3 | HG02129.hp2 NA18954.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-70+4183T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755895 | |||||||
| chr15:51755932 | G | A | 23 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0030 others(20): Show |
24 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-70+4220G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755932 | |||||||
| chr15:51755977 | A | G | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+4265A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755977 | |||||||
| chr15:51756054 | C | G | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+4342C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756054 | |||||||
| chr15:51756128 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+4416C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756128 | |||||||
| chr15:51756129 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+4417C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756129 | |||||||
| chr15:51756209 | G | A | 31 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(28): Show |
32 | HG00544.hp1 HG01106.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.-70+4497G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756209 | |||||||
| chr15:51756270 | T | C | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70+4558T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756270 | |||||||
| chr15:51756320 | T | G | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-70+4608T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756320 | |||||||
| chr15:51756379 | A | C | 1 | a0001c0001t0002g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-70+4667A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756379 | |||||||
| chr15:51756457 | C | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+4745C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756457 | |||||||
| chr15:51756493 | T | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+4781T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756493 | |||||||
| chr15:51756513 | A | G | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-70+4801A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756513 | |||||||
| chr15:51756514 | G | T | 2 | a0001c0001t0025g0345 a0001c0001t0025g0346 |
2 | HG02273.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-70+4802G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756514 | |||||||
| chr15:51756723 | G | C | 6 | a0001c0001t0007g0198 a0001c0001t0007g0200 a0001c0001t0007g0202 others(3): Show |
6 | HG02486.hp1 HG02818.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+5011G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756723 | |||||||
| chr15:51756762 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-70+5050G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756762 | |||||||
| chr15:51756767 | A | G | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.-70+5055A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756767 | |||||||
| chr15:51756894 | A | G | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-70+5182A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756894 | |||||||
| chr15:51757102 | A | G | 3 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0344 |
3 | HG02155.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-70+5390A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757102 | |||||||
| chr15:51757141 | C | T | 1 | a0001c0001t0001g0341 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-70+5429C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757141 | |||||||
| chr15:51757184 | C | G | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+5472C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757184 | |||||||
| chr15:51757216 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-70+5504A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757216 | |||||||
| chr15:51757244 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+5532A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757244 | |||||||
| chr15:51757350 | G | A | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.-70+5638G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757350 | |||||||
| chr15:51757383 | C | T | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-70+5671C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757383 | |||||||
| chr15:51757396 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+5684C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757396 | |||||||
| chr15:51757401 | C | CA | 22 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0278 others(19): Show |
23 | HG01109.hp2 HG01123.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.-70+5712dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | ||||||
| chr15:51757401 | CA | C | 25 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(22): Show |
29 | HG00639.hp1 HG00733.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-70+5712delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | ||||||
| chr15:51757401 | CAA | C | 43 | a0001c0001t0002g0049 a0001c0001t0002g0051 a0001c0001t0004g0050 others(40): Show |
46 | HG00544.hp1 HG00741.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.-70+5711_-70+5712d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | ||||||
| chr15:51757401 | CAAA | C | 123 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(120): Show |
134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-70+5710_-70+5712d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | ||||||
| chr15:51757581 | C | A | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-70+5869C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757581 | |||||||
| chr15:51757624 | A | G | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-70+5912A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757624 | |||||||
| chr15:51757696 | T | C | 1 | a0001c0001t0008g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-70+5984T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757696 | |||||||
| chr15:51757840 | G | A | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-70+6128G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757840 | |||||||
| chr15:51757894 | G | A | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-70+6182G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757894 | |||||||
| chr15:51757996 | C | G | 1 | a0001c0001t0008g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-70+6284C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757996 | |||||||
| chr15:51758037 | A | G | 1 | a0001c0001t0007g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-70+6325A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758037 | |||||||
| chr15:51758086 | T | G | 1 | a0001c0001t0056g0141 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-70+6374T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758086 | |||||||
| chr15:51758151 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-70+6439G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758151 | |||||||
| chr15:51758208 | A | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+6496A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758208 | |||||||
| chr15:51758314 | G | T | 1 | a0001c0001t0001g0336 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-70+6602G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758314 | |||||||
| chr15:51758416 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-70+6704G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758416 | |||||||
| chr15:51758502 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-70+6790C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758502 | |||||||
| chr15:51758699 | G | C | 1 | a0001c0001t0003g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-70+6987G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758699 | |||||||
| chr15:51758714 | A | T | 1 | a0001c0001t0001g0335 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-70+7002A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758714 | |||||||
| chr15:51758797 | G | A | 1 | a0001c0001t0006g0029 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-70+7085G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758797 | |||||||
| chr15:51758830 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+7118G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758830 | |||||||
| chr15:51758946 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-70+7234G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758946 | |||||||
| chr15:51759038 | ACT | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG01099.hp1 HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-70+7329_-70+7330d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51759038 | ||||||
| chr15:51759058 | A | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-7315A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759058 | |||||||
| chr15:51759199 | GT | G | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-69-7172delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51759199 | ||||||
| chr15:51759224 | G | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(8): Show |
13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-69-7149G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759224 | |||||||
| chr15:51759658 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-69-6715A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759658 | |||||||
| chr15:51759702 | A | C | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-69-6671A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759702 | |||||||
| chr15:51759840 | A | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-6533A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759840 | |||||||
| chr15:51759902 | G | T | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0333 others(1): Show |
4 | HG00642.hp1 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-6471G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759902 | |||||||
| chr15:51759961 | C | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-6412C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759961 | |||||||
| chr15:51760117 | C | A | 1 | a0001c0001t0019g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-69-6256C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760117 | |||||||
| chr15:51760511 | A | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-5862A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760511 | |||||||
| chr15:51760621 | A | G | 52 | a0001c0001t0003g0004 a0001c0001t0003g0203 a0001c0001t0003g0204 others(49): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-69-5752A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760621 | |||||||
| chr15:51760628 | A | G | 2 | a0001c0001t0016g0138 a0001c0001t0016g0139 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-5745A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760628 | |||||||
| chr15:51760670 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-69-5703G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760670 | |||||||
| chr15:51760731 | G | A | 9 | a0001c0001t0007g0018 a0001c0001t0007g0213 a0001c0001t0007g0214 others(6): Show |
10 | HG01255.hp1 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-5642G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760731 | |||||||
| chr15:51760814 | G | GA | 136 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(133): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-69-5550dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51760814 | ||||||
| chr15:51760959 | C | T | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-69-5414C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760959 | |||||||
| chr15:51761032 | T | C | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-69-5341T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761032 | |||||||
| chr15:51761048 | G | T | 2 | a0001c0001t0022g0255 a0001c0001t0022g0270 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-69-5325G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761048 | |||||||
| chr15:51761049 | G | T | 2 | a0001c0001t0022g0255 a0001c0001t0022g0270 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-69-5324G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761049 | |||||||
| chr15:51761080 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-69-5293G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761080 | |||||||
| chr15:51761193 | G | A | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-69-5180G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761193 | |||||||
| chr15:51761226 | CAA | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0329 a0001c0001t0001g0330 others(2): Show |
6 | HG00544.hp2 HG01934.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-69-5146_-69-5145d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761226 | |||||||
| chr15:51761249 | G | T | 1 | a0001c0001t0007g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-69-5124G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761249 | |||||||
| chr15:51761256 | ATGT | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(118): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-69-5113_-69-5111d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51761256 | ||||||
| chr15:51761347 | T | C | 1 | a0001c0001t0023g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-69-5026T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761347 | |||||||
| chr15:51761441 | T | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-4932T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761441 | |||||||
| chr15:51761446 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-4927G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761446 | |||||||
| chr15:51761570 | G | GA | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-69-4794dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51761570 | ||||||
| chr15:51761876 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-69-4497G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761876 | |||||||
| chr15:51761991 | C | CA | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-4374dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51761991 | ||||||
| chr15:51762085 | C | A | 1 | a0001c0001t0003g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-69-4288C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762085 | |||||||
| chr15:51762097 | C | T | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-69-4276C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762097 | |||||||
| chr15:51762106 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(118): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-69-4267G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762106 | |||||||
| chr15:51762301 | A | T | 1 | a0001c0001t0051g0313 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-69-4072A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762301 | |||||||
| chr15:51762328 | G | A | 22 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0030 others(19): Show |
23 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-69-4045G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762328 | |||||||
| chr15:51762436 | G | A | 105 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0001t0001g0248 others(102): Show |
106 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-69-3937G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762436 | |||||||
| chr15:51762445 | C | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-3928C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762445 | |||||||
| chr15:51762648 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-69-3725T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762648 | |||||||
| chr15:51762652 | C | T | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-3721C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762652 | |||||||
| chr15:51762678 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-69-3695C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762678 | |||||||
| chr15:51762853 | C | T | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-3520C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762853 | |||||||
| chr15:51762912 | T | C | 2 | a0001c0001t0006g0030 a0001c0001t0029g0031 |
2 | NA18946.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-69-3461T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762912 | |||||||
| chr15:51762913 | G | C | 1 | a0001c0001t0007g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-69-3460G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762913 | |||||||
| chr15:51762922 | C | T | 1 | a0001c0001t0023g0327 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-69-3451C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762922 | |||||||
| chr15:51762974 | T | G | 1 | a0001c0001t0007g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-69-3399T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762974 | |||||||
| chr15:51763053 | A | G | 1 | a0001c0001t0006g0029 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-69-3320A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763053 | |||||||
| chr15:51763060 | G | A | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-3313G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763060 | |||||||
| chr15:51763077 | G | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-3296G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763077 | |||||||
| chr15:51763101 | AT | A | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-69-3267delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51763101 | ||||||
| chr15:51763106 | T | A | 129 | a0001c0001t0001g0278 a0001c0001t0002g0001 a0001c0001t0002g0003 others(126): Show |
140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-69-3267T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763106 | |||||||
| chr15:51763106 | TA | T | 50 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(47): Show |
54 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.-69-3256delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51763106 | ||||||
| chr15:51763107 | A | T | 2 | a0001c0001t0008g0268 a0001c0001t0023g0244 |
2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-69-3266A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763107 | |||||||
| chr15:51763108 | A | T | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-3265A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763108 | |||||||
| chr15:51763131 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-3242G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763131 | |||||||
| chr15:51763143 | TGCCCAGG others(17): Show |
T | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-69-3228_-69-3205d others(26): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51763143 | ||||||
| chr15:51763203 | C | T | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-3170C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763203 | |||||||
| chr15:51763205 | T | C | 1 | a0001c0001t0017g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-69-3168T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763205 | |||||||
| chr15:51763272 | C | G | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-69-3101C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763272 | |||||||
| chr15:51763341 | A | G | 7 | a0001c0001t0009g0015 a0001c0001t0009g0159 a0001c0001t0009g0162 others(4): Show |
8 | NA18946.hp2 NA18957.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.-69-3032A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763341 | |||||||
| chr15:51763357 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-69-3016C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763357 | |||||||
| chr15:51763388 | T | C | 106 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0001t0001g0248 others(103): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-69-2985T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763388 | |||||||
| chr15:51763723 | T | G | 1 | a0001c0001t0001g0286 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-69-2650T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763723 | |||||||
| chr15:51763736 | G | T | 44 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(41): Show |
46 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.-69-2637G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763736 | |||||||
| chr15:51763837 | A | G | 1 | a0001c0001t0001g0339 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-69-2536A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763837 | |||||||
| chr15:51763974 | G | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-2399G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763974 | |||||||
| chr15:51764048 | T | G | 1 | a0001c0001t0002g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-2325T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764048 | |||||||
| chr15:51764049 | G | T | 1 | a0001c0001t0002g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-2324G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764049 | |||||||
| chr15:51764085 | T | TA | 38 | a0001c0001t0002g0049 a0001c0001t0005g0016 a0001c0001t0005g0170 others(35): Show |
40 | HG00544.hp1 HG01106.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.-69-2276dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51764085 | ||||||
| chr15:51764085 | TA | T | 147 | a0001c0001t0001g0150 a0001c0001t0002g0001 a0001c0001t0002g0003 others(144): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-69-2276delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51764085 | ||||||
| chr15:51764085 | TAA | T | 5 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-69-2277_-69-2276d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51764085 | ||||||
| chr15:51764178 | T | G | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-69-2195T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764178 | |||||||
| chr15:51764211 | A | G | 1 | a0001c0001t0016g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-69-2162A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764211 | |||||||
| chr15:51764254 | T | C | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-69-2119T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764254 | |||||||
| chr15:51764266 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-69-2107G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764266 | |||||||
| chr15:51764343 | A | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-2030A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764343 | |||||||
| chr15:51764377 | G | T | 2 | a0001c0001t0016g0138 a0001c0001t0016g0139 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-1996G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764377 | |||||||
| chr15:51764396 | A | C | 1 | a0001c0001t0002g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-1977A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764396 | |||||||
| chr15:51764440 | C | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-1933C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764440 | |||||||
| chr15:51764484 | G | A | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-1889G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764484 | |||||||
| chr15:51764556 | C | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-1817C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764556 | |||||||
| chr15:51764701 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-69-1672T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764701 | |||||||
| chr15:51764740 | G | C | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-1633G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764740 | |||||||
| chr15:51764807 | T | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-1566T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764807 | |||||||
| chr15:51764825 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-69-1548A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764825 | |||||||
| chr15:51765012 | A | AT | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-1351dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51765012 | ||||||
| chr15:51765030 | T | A | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-1343T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765030 | |||||||
| chr15:51765063 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0127 |
2 | NA19006.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-69-1310T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765063 | |||||||
| chr15:51765160 | C | T | 2 | a0001c0001t0003g0212 a0001c0001t0003g0233 |
2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-69-1213C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765160 | |||||||
| chr15:51765213 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-1160C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765213 | |||||||
| chr15:51765255 | C | A | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-69-1118C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765255 | |||||||
| chr15:51765517 | C | G | 1 | a0001c0001t0001g0274 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-69-856C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765517 | |||||||
| chr15:51765564 | A | C | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-69-809A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765564 | |||||||
| chr15:51765677 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-69-696C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765677 | |||||||
| chr15:51765743 | A | G | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-69-630A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765743 | |||||||
| chr15:51765772 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-69-601A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765772 | |||||||
| chr15:51765897 | T | C | 1 | a0001c0001t0017g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-69-476T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765897 | |||||||
| chr15:51765987 | A | G | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-386A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765987 | |||||||
| chr15:51765988 | T | C | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-385T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765988 | |||||||
| chr15:51766184 | A | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-189A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51766184 | |||||||
| chr15:51766747 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+180G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766747 | |||||||
| chr15:51766808 | G | A | 130 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(127): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.126+241G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766808 | |||||||
| chr15:51766879 | A | G | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+312A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766879 | |||||||
| chr15:51766892 | T | C | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.126+325T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766892 | |||||||
| chr15:51767031 | A | AT | 154 | a0001c0001t0001g0334 a0001c0001t0001g0339 a0001c0001t0002g0001 others(151): Show |
167 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.126+478dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 51767031 | ||||||
| chr15:51767031 | A | ATT | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+477_126+478dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 51767031 | ||||||
| chr15:51767085 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.126+518G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767085 | |||||||
| chr15:51767214 | C | T | 29 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(26): Show |
30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+647C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767214 | |||||||
| chr15:51767410 | G | T | 1 | a0001c0001t0049g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126+843G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767410 | |||||||
| chr15:51767634 | TA | T | 146 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(143): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.127-616delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 51767634 | ||||||
| chr15:51767769 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.127-493A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767769 | |||||||
| chr15:51767788 | A | T | 6 | a0001c0001t0007g0198 a0001c0001t0007g0200 a0001c0001t0007g0202 others(3): Show |
6 | HG02486.hp1 HG02818.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-474A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767788 | |||||||
| chr15:51767970 | A | G | 130 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(127): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.127-292A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767970 | |||||||
| chr15:51768095 | T | C | 2 | a0001c0001t0003g0212 a0001c0001t0003g0233 |
2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.127-167T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51768095 | |||||||
| chr15:51768110 | G | A | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.127-152G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51768110 | |||||||
| chr15:51768221 | G | A | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-41G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51768221 | |||||||
| chr15:51768460 | C | CT | 145 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.283+54dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51768460 | ||||||
| chr15:51768460 | C | CTTTT | 26 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0173 others(23): Show |
27 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.283+51_283+54dupTT others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51768460 | ||||||
| chr15:51768601 | G | A | 21 | a0001c0001t0004g0002 a0001c0001t0004g0050 a0001c0001t0004g0054 others(18): Show |
24 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+183G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768601 | |||||||
| chr15:51768609 | A | G | 130 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(127): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.283+191A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768609 | |||||||
| chr15:51768703 | T | C | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0018g0257 others(2): Show |
5 | HG01109.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+285T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768703 | |||||||
| chr15:51768731 | A | AGATTCAG others(71): Show |
6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+394_283+471dup others(78): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51768731 | ||||||
| chr15:51768754 | C | T | 130 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(127): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.283+336C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768754 | |||||||
| chr15:51768784 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.283+366G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768784 | |||||||
| chr15:51768890 | G | T | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.283+472G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768890 | |||||||
| chr15:51768910 | T | C | 1 | a0001c0001t0003g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.283+492T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768910 | |||||||
| chr15:51768927 | T | C | 337 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0001t0001g0248 others(334): Show |
359 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.283+509T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768927 | |||||||
| chr15:51769017 | T | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+599T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769017 | |||||||
| chr15:51769025 | A | G | 1 | a0001c0001t0035g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.283+607A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769025 | |||||||
| chr15:51769324 | A | T | 4 | a0001c0001t0015g0209 a0001c0001t0015g0210 a0001c0001t0015g0211 others(1): Show |
4 | HG01081.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+906A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769324 | |||||||
| chr15:51769536 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.283+1118G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769536 | |||||||
| chr15:51769622 | G | T | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+1204G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769622 | |||||||
| chr15:51769743 | A | G | 15 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(12): Show |
16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+1325A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769743 | |||||||
| chr15:51769761 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.283+1343G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769761 | |||||||
| chr15:51769772 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.283+1354C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769772 | |||||||
| chr15:51769824 | A | C | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.283+1406A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769824 | |||||||
| chr15:51769898 | A | G | 1 | a0001c0001t0007g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283+1480A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769898 | |||||||
| chr15:51770313 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+1895T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770313 | |||||||
| chr15:51770480 | C | A | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.283+2062C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770480 | |||||||
| chr15:51770487 | T | C | 1 | a0001c0001t0006g0030 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.283+2069T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770487 | |||||||
| chr15:51770510 | C | T | 15 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(12): Show |
16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+2092C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770510 | |||||||
| chr15:51770584 | C | T | 1 | a0001c0001t0005g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.283+2166C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770584 | |||||||
| chr15:51770623 | A | G | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.283+2205A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770623 | |||||||
| chr15:51770851 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.283+2433G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770851 | |||||||
| chr15:51770910 | G | A | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.283+2492G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770910 | |||||||
| chr15:51770982 | T | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+2564T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770982 | |||||||
| chr15:51771139 | G | A | 1 | a0001c0001t0006g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.284-2573G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771139 | |||||||
| chr15:51771242 | C | T | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.284-2470C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771242 | |||||||
| chr15:51771282 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0033g0003 |
3 | HG02451.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.284-2430C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771282 | |||||||
| chr15:51771301 | A | G | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.284-2411A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771301 | |||||||
| chr15:51771339 | C | T | 1 | a0001c0001t0004g0078 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.284-2373C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771339 | |||||||
| chr15:51771348 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.284-2364A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771348 | |||||||
| chr15:51771542 | C | G | 176 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(173): Show |
191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.284-2170C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771542 | |||||||
| chr15:51771553 | A | T | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.284-2159A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771553 | |||||||
| chr15:51771928 | T | A | 1 | a0001c0001t0027g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.284-1784T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771928 | |||||||
| chr15:51772033 | T | C | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1679T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772033 | |||||||
| chr15:51772089 | G | A | 16 | a0001c0001t0005g0170 a0001c0001t0005g0172 a0001c0001t0005g0174 others(13): Show |
16 | HG01496.hp1 HG01934.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-1623G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772089 | |||||||
| chr15:51772179 | C | T | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.284-1533C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772179 | |||||||
| chr15:51772216 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-1496G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772216 | |||||||
| chr15:51772219 | A | C | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.284-1493A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772219 | |||||||
| chr15:51772319 | G | A | 16 | a0001c0001t0008g0196 a0001c0001t0008g0253 a0001c0001t0008g0254 others(13): Show |
16 | HG01358.hp2 HG02056.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-1393G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772319 | |||||||
| chr15:51772480 | G | A | 245 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(242): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.284-1232G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772480 | |||||||
| chr15:51772790 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(78): Show |
90 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.284-922G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772790 | |||||||
| chr15:51773028 | C | T | 127 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(124): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.284-684C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773028 | |||||||
| chr15:51773212 | A | G | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.284-500A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773212 | |||||||
| chr15:51773274 | A | C | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.284-438A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773274 | |||||||
| chr15:51773328 | C | A | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.284-384C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773328 | |||||||
| chr15:51773435 | A | G | 55 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(52): Show |
60 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.284-277A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773435 | |||||||
| chr15:51773623 | A | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.284-89A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773623 | |||||||
| chr15:51773628 | C | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-84C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773628 | |||||||
| chr15:51773672 | C | CA | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.284-39dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51773672 | ||||||
| chr15:51773992 | A | C | 245 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(242): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.406+158A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51773992 | |||||||
| chr15:51774015 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.406+181G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774015 | |||||||
| chr15:51774111 | G | A | 134 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(131): Show |
147 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.406+277G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774111 | |||||||
| chr15:51774124 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.406+290C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774124 | |||||||
| chr15:51774281 | A | G | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+447A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774281 | |||||||
| chr15:51774298 | A | C | 1 | a0001c0001t0002g0109 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.406+464A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774298 | |||||||
| chr15:51774306 | A | T | 1 | a0001c0001t0010g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406+472A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774306 | |||||||
| chr15:51774438 | T | C | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.406+604T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774438 | |||||||
| chr15:51774464 | G | A | 1 | a0001c0001t0012g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.406+630G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774464 | |||||||
| chr15:51774594 | A | G | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+760A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774594 | |||||||
| chr15:51774739 | A | G | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+905A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774739 | |||||||
| chr15:51774927 | A | C | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1093A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774927 | |||||||
| chr15:51774954 | A | G | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+1120A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774954 | |||||||
| chr15:51775074 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(125): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.406+1240C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775074 | |||||||
| chr15:51775262 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.406+1428A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775262 | |||||||
| chr15:51775288 | T | C | 1 | a0001c0001t0027g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.406+1454T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775288 | |||||||
| chr15:51775335 | T | C | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.406+1501T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775335 | |||||||
| chr15:51775458 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(45): Show |
53 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.407-1474A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775458 | |||||||
| chr15:51775563 | C | CT | 56 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(53): Show |
58 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.407-1364dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775563 | ||||||
| chr15:51775569 | C | T | 117 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(114): Show |
130 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.407-1363C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775569 | |||||||
| chr15:51775570 | C | CT | 25 | a0001c0001t0001g0152 a0001c0001t0001g0302 a0001c0001t0001g0309 others(22): Show |
27 | HG00544.hp2 HG01433.hp2 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.407-1337dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | ||||||
| chr15:51775570 | C | CTT | 89 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(86): Show |
96 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.407-1338_407-1337d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | ||||||
| chr15:51775570 | C | CTTT | 16 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0087 others(13): Show |
16 | HG00735.hp1 HG01106.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.407-1339_407-1337d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | ||||||
| chr15:51775570 | C | T | 57 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(54): Show |
59 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.407-1362C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775570 | |||||||
| chr15:51775570 | CT | C | 15 | a0001c0001t0001g0266 a0001c0001t0001g0278 a0001c0001t0001g0308 others(12): Show |
15 | HG00323.hp2 HG00408.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.407-1337delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | ||||||
| chr15:51775575 | T | C | 1 | a0001c0001t0028g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.407-1357T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775575 | |||||||
| chr15:51775576 | T | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.407-1356T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775576 | |||||||
| chr15:51775579 | T | C | 1 | a0001c0001t0016g0138 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.407-1353T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775579 | |||||||
| chr15:51775670 | G | C | 162 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(159): Show |
176 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.407-1262G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775670 | |||||||
| chr15:51775708 | G | A | 2 | a0001c0001t0003g0203 a0001c0001t0003g0204 |
2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.407-1224G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775708 | |||||||
| chr15:51776070 | G | C | 21 | a0001c0001t0004g0002 a0001c0001t0004g0050 a0001c0001t0004g0054 others(18): Show |
24 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.407-862G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776070 | |||||||
| chr15:51776073 | T | C | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.407-859T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776073 | |||||||
| chr15:51776113 | T | G | 1 | a0001c0001t0016g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.407-819T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776113 | |||||||
| chr15:51776117 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.407-815C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776117 | |||||||
| chr15:51776211 | A | G | 4 | a0001c0001t0001g0277 a0001c0001t0001g0286 a0001c0001t0001g0324 others(1): Show |
4 | NA18612.hp2 NA18982.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-721A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776211 | |||||||
| chr15:51776300 | G | A | 1 | a0001c0001t0049g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.407-632G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776300 | |||||||
| chr15:51776400 | C | T | 1 | a0001c0001t0005g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.407-532C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776400 | |||||||
| chr15:51776416 | T | C | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.407-516T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776416 | |||||||
| chr15:51776677 | T | C | 129 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(126): Show |
140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.407-255T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776677 | |||||||
| chr15:51776712 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(8): Show |
13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.407-220A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776712 | |||||||
| chr15:51776726 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-206A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776726 | |||||||
| chr15:51776786 | T | C | 1 | a0001c0001t0008g0253 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.407-146T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776786 | |||||||
| chr15:51776810 | G | A | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.407-122G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776810 | |||||||
| chr15:51776917 | G | A | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.407-15G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776917 | |||||||
| chr15:51777033 | A | C | 1 | a0001c0001t0007g0214 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.493+15A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777033 | |||||||
| chr15:51777065 | A | G | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493+47A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777065 | |||||||
| chr15:51777081 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.493+63G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777081 | |||||||
| chr15:51777096 | T | C | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.493+78T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777096 | |||||||
| chr15:51777193 | G | A | 4 | a0001c0001t0006g0039 a0001c0001t0006g0041 a0001c0001t0040g0040 others(1): Show |
4 | NA18964.hp1 NA19003.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+175G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777193 | |||||||
| chr15:51777544 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.493+526T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777544 | |||||||
| chr15:51777570 | C | T | 3 | a0001c0001t0001g0291 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | NA18961.hp2 NA19001.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.493+552C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777570 | |||||||
| chr15:51777573 | G | A | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+555G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777573 | |||||||
| chr15:51777638 | C | T | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+620C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777638 | |||||||
| chr15:51777643 | A | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+625A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777643 | |||||||
| chr15:51777747 | A | G | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.493+729A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777747 | |||||||
| chr15:51778019 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.493+1001T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778019 | |||||||
| chr15:51778051 | G | A | 15 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(12): Show |
16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+1033G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778051 | |||||||
| chr15:51778174 | A | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+1156A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778174 | |||||||
| chr15:51778189 | G | A | 1 | a0001c0001t0006g0042 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.493+1171G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778189 | |||||||
| chr15:51778254 | C | T | 129 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(126): Show |
140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.493+1236C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778254 | |||||||
| chr15:51778323 | C | G | 1 | a0001c0001t0027g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.493+1305C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778323 | |||||||
| chr15:51778341 | T | G | 1 | a0001c0001t0050g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.493+1323T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778341 | |||||||
| chr15:51778349 | G | C | 1 | a0001c0001t0003g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.493+1331G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778349 | |||||||
| chr15:51778413 | C | T | 1 | a0001c0001t0028g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.493+1395C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778413 | |||||||
| chr15:51778426 | T | A | 24 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0030 others(21): Show |
25 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.493+1408T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778426 | |||||||
| chr15:51778453 | A | T | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.493+1435A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778453 | |||||||
| chr15:51778467 | C | A | 1 | a0001c0001t0002g0127 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.493+1449C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778467 | |||||||
| chr15:51778507 | T | TA | 120 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(117): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.493+1502dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778507 | ||||||
| chr15:51778508 | A | T | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.493+1490A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778508 | |||||||
| chr15:51778517 | A | AG | 8 | a0001c0001t0002g0127 a0001c0001t0012g0022 a0001c0001t0012g0129 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+1499_493+1500i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778517 | |||||||
| chr15:51778638 | T | G | 15 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(12): Show |
16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+1620T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778638 | |||||||
| chr15:51778643 | C | CT | 125 | a0001c0001t0001g0276 a0001c0001t0001g0286 a0001c0001t0001g0289 others(122): Show |
135 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.493+1651dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | ||||||
| chr15:51778643 | C | CTT | 31 | a0001c0001t0002g0010 a0001c0001t0002g0027 a0001c0001t0002g0057 others(28): Show |
32 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.493+1650_493+1651d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | ||||||
| chr15:51778643 | CT | C | 33 | a0001c0001t0003g0004 a0001c0001t0003g0205 a0001c0001t0003g0206 others(30): Show |
39 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.493+1651delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | ||||||
| chr15:51778643 | CTT | C | 15 | a0001c0001t0001g0278 a0001c0001t0001g0294 a0001c0001t0001g0337 others(12): Show |
16 | HG00140.hp2 HG00733.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.493+1650_493+1651d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | ||||||
| chr15:51778643 | CTTT | C | 29 | a0001c0001t0002g0089 a0001c0001t0005g0016 a0001c0001t0005g0170 others(26): Show |
31 | HG00544.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.493+1649_493+1651d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | ||||||
| chr15:51778667 | T | C | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.493+1649T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778667 | |||||||
| chr15:51778747 | T | G | 9 | a0001c0001t0001g0272 a0001c0001t0001g0277 a0001c0001t0001g0286 others(6): Show |
9 | HG02155.hp2 NA18612.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.493+1729T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778747 | |||||||
| chr15:51778810 | A | G | 17 | a0001c0001t0003g0004 a0001c0001t0003g0203 a0001c0001t0003g0204 others(14): Show |
20 | HG00639.hp2 HG00733.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.493+1792A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778810 | |||||||
| chr15:51778830 | A | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 |
3 | HG02615.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.493+1812A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778830 | |||||||
| chr15:51778980 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+1962A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778980 | |||||||
| chr15:51779089 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0146 a0001c0001t0024g0012 |
5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-1955G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779089 | |||||||
| chr15:51779241 | C | T | 1 | a0001c0001t0005g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.494-1803C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779241 | |||||||
| chr15:51779242 | G | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-1802G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779242 | |||||||
| chr15:51779273 | T | A | 1 | a0001c0001t0001g0344 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.494-1771T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779273 | |||||||
| chr15:51779411 | C | T | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-1633C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779411 | |||||||
| chr15:51779442 | A | G | 1 | a0001c0001t0027g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.494-1602A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779442 | |||||||
| chr15:51779460 | A | G | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.494-1584A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779460 | |||||||
| chr15:51779573 | C | T | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.494-1471C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779573 | |||||||
| chr15:51779686 | C | CT | 33 | a0001c0001t0001g0344 a0001c0001t0005g0016 a0001c0001t0005g0170 others(30): Show |
34 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.494-1346dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51779686 | ||||||
| chr15:51779686 | CT | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.494-1346delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51779686 | ||||||
| chr15:51779743 | C | A | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.494-1301C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779743 | |||||||
| chr15:51779765 | C | G | 1 | a0001c0001t0006g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.494-1279C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779765 | |||||||
| chr15:51779940 | C | A | 7 | a0001c0001t0009g0015 a0001c0001t0009g0159 a0001c0001t0009g0162 others(4): Show |
8 | NA18946.hp2 NA18957.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-1104C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779940 | |||||||
| chr15:51779941 | C | A | 1 | a0001c0001t0029g0031 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.494-1103C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779941 | |||||||
| chr15:51780016 | T | C | 1 | a0001c0001t0011g0296 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.494-1028T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780016 | |||||||
| chr15:51780023 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.494-1021G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780023 | |||||||
| chr15:51780218 | C | T | 1 | a0001c0001t0027g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.494-826C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780218 | |||||||
| chr15:51780240 | C | G | 1 | a0001c0001t0037g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.494-804C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780240 | |||||||
| chr15:51780400 | A | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(121): Show |
136 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.494-644A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780400 | |||||||
| chr15:51780437 | T | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0088 others(4): Show |
9 | HG02074.hp1 HG02129.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-607T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780437 | |||||||
| chr15:51780752 | C | T | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-292C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780752 | |||||||
| chr15:51781210 | A | ATCATGAG others(37): Show |
1 | a0001c0001t0001g0344 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.624+40_624+83dupTG others(42): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781210 | ||||||
| chr15:51781492 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.624+318G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781492 | |||||||
| chr15:51781587 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+413G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781587 | |||||||
| chr15:51781605 | T | A | 38 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(35): Show |
39 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+431T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781605 | |||||||
| chr15:51781619 | G | A | 140 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(137): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.624+445G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781619 | |||||||
| chr15:51781651 | T | C | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+477T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781651 | |||||||
| chr15:51781695 | G | A | 31 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(28): Show |
32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.624+521G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781695 | |||||||
| chr15:51781705 | A | G | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(119): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.624+531A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781705 | |||||||
| chr15:51781718 | T | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(119): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.624+544T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781718 | |||||||
| chr15:51781803 | G | GGA | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.624+649_624+650dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781803 | ||||||
| chr15:51781803 | G | GGAGA | 74 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(71): Show |
80 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.624+647_624+650dup others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781803 | ||||||
| chr15:51781821 | A | AGT | 135 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
147 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.624+648_624+649ins others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781821 | ||||||
| chr15:51781821 | A | AGTGT | 6 | a0001c0001t0002g0024 a0001c0001t0002g0085 a0001c0001t0002g0086 others(3): Show |
6 | HG01891.hp1 HG01928.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+648_624+649ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781821 | ||||||
| chr15:51781823 | A | AGAGAGAG others(3): Show |
2 | a0001c0001t0001g0151 a0001c0001t0018g0257 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.624+650_624+651ins others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | ||||||
| chr15:51781823 | A | AGAGAGAG others(1): Show |
10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(7): Show |
12 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+650_624+651ins others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | ||||||
| chr15:51781823 | A | AGAGAGT | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+650_624+651ins others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | ||||||
| chr15:51781823 | A | AGAGT | 5 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0012g0130 others(2): Show |
5 | HG00738.hp1 HG01081.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+650_624+651ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | ||||||
| chr15:51781823 | A | AGT | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0324 others(3): Show |
6 | HG00639.hp1 HG00733.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+668_624+669dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | ||||||
| chr15:51781823 | A | AGTGT | 6 | a0001c0001t0005g0170 a0001c0001t0005g0175 a0001c0001t0005g0177 others(3): Show |
6 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+666_624+669dup others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | ||||||
| chr15:51781823 | A | T | 143 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(140): Show |
155 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.624+649A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781823 | |||||||
| chr15:51781824 | G | T | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.624+650G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781824 | |||||||
| chr15:51781825 | T | A | 6 | a0001c0001t0003g0204 a0001c0001t0003g0222 a0001c0001t0003g0223 others(3): Show |
6 | HG00323.hp2 HG01255.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+651T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781825 | |||||||
| chr15:51781983 | A | T | 1 | a0001c0001t0001g0314 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.625-738A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781983 | |||||||
| chr15:51782047 | A | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.625-674A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782047 | |||||||
| chr15:51782324 | A | G | 1 | a0001c0001t0049g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.625-397A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782324 | |||||||
| chr15:51782376 | G | A | 31 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(28): Show |
32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.625-345G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782376 | |||||||
| chr15:51782427 | G | A | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.625-294G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782427 | |||||||
| chr15:51782494 | GACACTCA others(5): Show |
G | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.625-224_625-213del others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51782494 | ||||||
| chr15:51782648 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.625-73G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782648 | |||||||
| chr15:51783060 | T | C | 1 | a0001c0001t0008g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.732+232T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783060 | |||||||
| chr15:51783271 | C | T | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.732+443C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783271 | |||||||
| chr15:51783398 | C | T | 31 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(28): Show |
32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+570C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783398 | |||||||
| chr15:51783406 | C | T | 1 | a0001c0001t0023g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.732+578C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783406 | |||||||
| chr15:51783479 | CA | C | 240 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(237): Show |
263 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.732+663delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783479 | ||||||
| chr15:51783520 | A | T | 1 | a0001c0001t0001g0339 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.732+692A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783520 | |||||||
| chr15:51783745 | T | TGATA | 81 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0148 others(78): Show |
86 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.732+962_732+965dup others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | ||||||
| chr15:51783745 | T | TGATAGAT others(1): Show |
33 | a0001c0001t0001g0155 a0001c0001t0001g0250 a0001c0001t0001g0276 others(30): Show |
34 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.732+958_732+965dup others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | ||||||
| chr15:51783745 | T | TGATAGAT others(5): Show |
2 | a0001c0001t0001g0341 a0001c0001t0014g0321 |
2 | NA18967.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.732+954_732+965dup others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | ||||||
| chr15:51783745 | T | TGATAGAT others(13): Show |
1 | a0001c0001t0005g0183 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.732+946_732+965dup others(20): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | ||||||
| chr15:51783745 | TGATA | T | 22 | a0001c0001t0001g0274 a0001c0001t0003g0206 a0001c0001t0003g0223 others(19): Show |
23 | HG00735.hp2 HG01081.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+962_732+965del others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | ||||||
| chr15:51783745 | TGATAGAT others(1): Show |
T | 9 | a0001c0001t0001g0152 a0001c0001t0007g0213 a0001c0001t0007g0214 others(6): Show |
9 | HG01255.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.732+958_732+965del others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | ||||||
| chr15:51783775 | A | ATAGATAG others(5): Show |
2 | a0001c0001t0006g0033 a0001c0001t0006g0042 |
2 | NA19077.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.732+958_732+959ins others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783775 | ||||||
| chr15:51783775 | A | ATAGATAG others(1): Show |
10 | a0001c0001t0006g0006 a0001c0001t0006g0034 a0001c0001t0006g0035 others(7): Show |
11 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+954_732+955ins others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783775 | ||||||
| chr15:51783775 | A | ATAGG | 20 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(17): Show |
20 | HG01433.hp1 HG01891.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.732+950_732+951ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783775 | ||||||
| chr15:51783775 | A | G | 89 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(86): Show |
99 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.732+947A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783775 | |||||||
| chr15:51783791 | A | ATAGG | 4 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(1): Show |
4 | NA18747.hp1 NA18971.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+965_732+966ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783791 | ||||||
| chr15:51783791 | A | G | 1 | a0001c0001t0013g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.732+963A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783791 | |||||||
| chr15:51783887 | T | C | 1 | a0001c0001t0018g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732+1059T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783887 | |||||||
| chr15:51784025 | C | T | 15 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(12): Show |
16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+1197C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784025 | |||||||
| chr15:51784047 | T | C | 1 | a0001c0001t0008g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.732+1219T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784047 | |||||||
| chr15:51784199 | T | G | 125 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(122): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.732+1371T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784199 | |||||||
| chr15:51784325 | C | CCA | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+1497_732+1498i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784325 | |||||||
| chr15:51784326 | G | T | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+1498G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784326 | |||||||
| chr15:51784429 | T | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+1601T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784429 | |||||||
| chr15:51784540 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+1712A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784540 | |||||||
| chr15:51784608 | T | A | 38 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(35): Show |
39 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.732+1780T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784608 | |||||||
| chr15:51784659 | A | G | 1 | a0001c0001t0016g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.732+1831A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784659 | |||||||
| chr15:51784764 | T | G | 22 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0030 others(19): Show |
23 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+1936T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784764 | |||||||
| chr15:51784844 | C | A | 180 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0152 others(177): Show |
197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.732+2016C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784844 | |||||||
| chr15:51784959 | A | T | 1 | a0001c0001t0007g0214 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.732+2131A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784959 | |||||||
| chr15:51785057 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.732+2229C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785057 | |||||||
| chr15:51785135 | G | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+2307G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785135 | |||||||
| chr15:51785139 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0330 |
3 | HG01934.hp1 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.732+2311G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785139 | |||||||
| chr15:51785184 | G | A | 1 | a0001c0001t0008g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.732+2356G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785184 | |||||||
| chr15:51785275 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+2447G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785275 | |||||||
| chr15:51785411 | C | CA | 25 | a0001c0001t0005g0016 a0001c0001t0005g0172 a0001c0001t0005g0173 others(22): Show |
26 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.732+2605dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | ||||||
| chr15:51785411 | CA | C | 268 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0001t0001g0248 others(265): Show |
286 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.732+2605delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | ||||||
| chr15:51785411 | CAA | C | 16 | a0001c0001t0004g0070 a0001c0001t0004g0071 a0001c0001t0006g0036 others(13): Show |
18 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.732+2604_732+2605d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | ||||||
| chr15:51785411 | CAAA | C | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+2603_732+2605d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | ||||||
| chr15:51785532 | G | A | 38 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(35): Show |
39 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.732+2704G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785532 | |||||||
| chr15:51785962 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.732+3134A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785962 | |||||||
| chr15:51786038 | G | A | 163 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(160): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.732+3210G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786038 | |||||||
| chr15:51786154 | A | G | 15 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(12): Show |
16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+3326A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786154 | |||||||
| chr15:51786206 | C | T | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+3378C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786206 | |||||||
| chr15:51786282 | G | A | 32 | a0001c0001t0002g0097 a0001c0001t0005g0016 a0001c0001t0005g0170 others(29): Show |
33 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.732+3454G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786282 | |||||||
| chr15:51786366 | C | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(121): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.732+3538C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786366 | |||||||
| chr15:51786615 | G | A | 52 | a0001c0001t0003g0004 a0001c0001t0003g0203 a0001c0001t0003g0204 others(49): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.732+3787G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786615 | |||||||
| chr15:51786716 | A | G | 1 | a0001c0001t0010g0116 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.732+3888A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786716 | |||||||
| chr15:51786964 | A | T | 28 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(25): Show |
29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.732+4136A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786964 | |||||||
| chr15:51787129 | CCG | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(8): Show |
13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.732+4305_732+4306d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51787129 | ||||||
| chr15:51787275 | G | C | 1 | a0001c0001t0004g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.732+4447G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787275 | |||||||
| chr15:51787311 | G | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.732+4483G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787311 | |||||||
| chr15:51787354 | G | C | 1 | a0001c0001t0035g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.732+4526G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787354 | |||||||
| chr15:51787402 | G | C | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+4574G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787402 | |||||||
| chr15:51787662 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.732+4834T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787662 | |||||||
| chr15:51787672 | A | G | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.732+4844A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787672 | |||||||
| chr15:51787752 | C | T | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+4924C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787752 | |||||||
| chr15:51788024 | A | G | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.732+5196A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788024 | |||||||
| chr15:51788182 | A | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(119): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.732+5354A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788182 | |||||||
| chr15:51788344 | A | G | 15 | a0001c0001t0007g0018 a0001c0001t0007g0198 a0001c0001t0007g0200 others(12): Show |
16 | HG01255.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+5516A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788344 | |||||||
| chr15:51788368 | G | C | 177 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(174): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.732+5540G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788368 | |||||||
| chr15:51788467 | G | A | 1 | a0001c0001t0004g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.732+5639G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788467 | |||||||
| chr15:51788473 | C | A | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+5645C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788473 | |||||||
| chr15:51788518 | G | A | 2 | a0001c0001t0016g0138 a0001c0001t0016g0139 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+5690G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788518 | |||||||
| chr15:51788606 | T | C | 139 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(136): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.732+5778T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788606 | |||||||
| chr15:51788611 | G | C | 3 | a0001c0001t0008g0254 a0001c0001t0008g0260 a0001c0001t0008g0267 |
3 | NA18969.hp2 NA19002.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.732+5783G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788611 | |||||||
| chr15:51788829 | A | G | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6001A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788829 | |||||||
| chr15:51788836 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6008T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788836 | |||||||
| chr15:51788839 | C | A | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6011C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788839 | |||||||
| chr15:51788871 | T | A | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6043T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788871 | |||||||
| chr15:51788880 | C | T | 1 | a0001c0001t0038g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.732+6052C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788880 | |||||||
| chr15:51788922 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6094G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788922 | |||||||
| chr15:51788927 | C | G | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6099C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788927 | |||||||
| chr15:51788932 | T | G | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6104T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788932 | |||||||
| chr15:51788942 | A | G | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6114A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788942 | |||||||
| chr15:51788949 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6121T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788949 | |||||||
| chr15:51788953 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6125T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788953 | |||||||
| chr15:51788970 | G | A | 1 | a0001c0001t0008g0260 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.732+6142G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788970 | |||||||
| chr15:51788974 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6146G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788974 | |||||||
| chr15:51789037 | A | G | 15 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0032 others(12): Show |
16 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+6209A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789037 | |||||||
| chr15:51789141 | C | T | 17 | a0001c0001t0008g0196 a0001c0001t0008g0253 a0001c0001t0008g0254 others(14): Show |
17 | HG01358.hp2 HG02056.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.732+6313C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789141 | |||||||
| chr15:51789242 | A | G | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.732+6414A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789242 | |||||||
| chr15:51789314 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.732+6486G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789314 | |||||||
| chr15:51789401 | G | A | 2 | a0001c0001t0005g0182 a0001c0001t0005g0184 |
2 | NA18747.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.732+6573G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789401 | |||||||
| chr15:51789428 | A | G | 1 | a0001c0001t0054g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.732+6600A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789428 | |||||||
| chr15:51789445 | G | A | 17 | a0001c0001t0008g0196 a0001c0001t0008g0253 a0001c0001t0008g0254 others(14): Show |
17 | HG01358.hp2 HG02056.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.732+6617G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789445 | |||||||
| chr15:51789577 | G | A | 1 | a0001c0001t0026g0245 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.732+6749G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789577 | |||||||
| chr15:51789584 | C | T | 163 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(160): Show |
177 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.732+6756C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789584 | |||||||
| chr15:51789600 | A | G | 31 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(28): Show |
32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+6772A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789600 | |||||||
| chr15:51789601 | T | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+6773T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789601 | |||||||
| chr15:51789640 | C | T | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+6812C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789640 | |||||||
| chr15:51789816 | A | G | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(119): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.732+6988A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789816 | |||||||
| chr15:51789862 | G | T | 1 | a0001c0001t0018g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+7034G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789862 | |||||||
| chr15:51789885 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.732+7057T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789885 | |||||||
| chr15:51789923 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.732+7095G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789923 | |||||||
| chr15:51790012 | A | G | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.732+7184A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790012 | |||||||
| chr15:51790049 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.732+7221C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790049 | |||||||
| chr15:51790074 | G | A | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+7246G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790074 | |||||||
| chr15:51790151 | C | G | 1 | a0001c0001t0001g0347 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.732+7323C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790151 | |||||||
| chr15:51790233 | C | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+7405C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790233 | |||||||
| chr15:51790357 | A | G | 1 | a0001c0001t0028g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.732+7529A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790357 | |||||||
| chr15:51790408 | G | T | 1 | a0001c0001t0009g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.732+7580G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790408 | |||||||
| chr15:51790449 | C | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+7621C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790449 | |||||||
| chr15:51790468 | G | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+7640G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790468 | |||||||
| chr15:51790561 | G | A | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-7636G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790561 | |||||||
| chr15:51790633 | G | A | 2 | a0001c0001t0003g0222 a0001c0001t0003g0224 |
2 | HG01255.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.733-7564G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790633 | |||||||
| chr15:51790656 | A | G | 1 | a0001c0001t0007g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.733-7541A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790656 | |||||||
| chr15:51790823 | C | T | 9 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(6): Show |
10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-7374C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790823 | |||||||
| chr15:51790849 | G | A | 2 | a0001c0001t0020g0062 a0001c0001t0020g0113 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.733-7348G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790849 | |||||||
| chr15:51790982 | A | G | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.733-7215A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790982 | |||||||
| chr15:51791160 | C | T | 52 | a0001c0001t0003g0004 a0001c0001t0003g0203 a0001c0001t0003g0204 others(49): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.733-7037C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791160 | |||||||
| chr15:51791504 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-6693A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791504 | |||||||
| chr15:51791665 | C | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-6532C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791665 | |||||||
| chr15:51791715 | A | G | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-6482A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791715 | |||||||
| chr15:51791728 | C | A | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-6469C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791728 | |||||||
| chr15:51791729 | A | C | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-6468A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791729 | |||||||
| chr15:51791732 | C | A | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-6465C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791732 | |||||||
| chr15:51791764 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.733-6433C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791764 | |||||||
| chr15:51792033 | G | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(121): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.733-6164G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792033 | |||||||
| chr15:51792110 | C | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-6087C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792110 | |||||||
| chr15:51792220 | C | A | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-5977C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792220 | |||||||
| chr15:51792253 | T | C | 1 | a0001c0001t0007g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.733-5944T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792253 | |||||||
| chr15:51792265 | C | T | 23 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0030 others(20): Show |
24 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.733-5932C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792265 | |||||||
| chr15:51792317 | C | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-5880C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792317 | |||||||
| chr15:51792328 | G | A | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-5869G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792328 | |||||||
| chr15:51792409 | T | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(121): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.733-5788T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792409 | |||||||
| chr15:51792721 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733-5476G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792721 | |||||||
| chr15:51792780 | C | T | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-5417C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792780 | |||||||
| chr15:51792885 | G | A | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.733-5312G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792885 | |||||||
| chr15:51792951 | G | T | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-5246G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792951 | |||||||
| chr15:51793178 | A | T | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-5019A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793178 | |||||||
| chr15:51793329 | A | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 |
3 | HG02615.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.733-4868A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793329 | |||||||
| chr15:51793364 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.733-4833A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793364 | |||||||
| chr15:51793439 | G | A | 2 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.733-4758G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793439 | |||||||
| chr15:51793503 | T | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(8): Show |
13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.733-4694T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793503 | |||||||
| chr15:51793618 | C | T | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-4579C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793618 | |||||||
| chr15:51793777 | G | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4420G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793777 | |||||||
| chr15:51793807 | G | A | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-4390G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793807 | |||||||
| chr15:51793818 | T | G | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-4379T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793818 | |||||||
| chr15:51793879 | T | A | 7 | a0001c0001t0005g0170 a0001c0001t0005g0175 a0001c0001t0005g0177 others(4): Show |
7 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4318T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793879 | |||||||
| chr15:51793880 | G | T | 7 | a0001c0001t0005g0170 a0001c0001t0005g0175 a0001c0001t0005g0177 others(4): Show |
7 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4317G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793880 | |||||||
| chr15:51793881 | C | T | 7 | a0001c0001t0005g0170 a0001c0001t0005g0175 a0001c0001t0005g0177 others(4): Show |
7 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4316C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793881 | |||||||
| chr15:51793974 | G | A | 1 | a0001c0001t0008g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.733-4223G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793974 | |||||||
| chr15:51794092 | G | C | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-4105G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794092 | |||||||
| chr15:51794105 | C | T | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.733-4092C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794105 | |||||||
| chr15:51794214 | C | T | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-3983C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794214 | |||||||
| chr15:51794225 | G | A | 3 | a0001c0001t0008g0254 a0001c0001t0008g0260 a0001c0001t0008g0267 |
3 | NA18969.hp2 NA19002.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.733-3972G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794225 | |||||||
| chr15:51794532 | T | C | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.733-3665T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794532 | |||||||
| chr15:51794569 | G | C | 1 | a0001c0001t0002g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.733-3628G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794569 | |||||||
| chr15:51794630 | T | A | 1 | a0001c0001t0013g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-3567T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794630 | |||||||
| chr15:51794660 | C | A | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-3537C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794660 | |||||||
| chr15:51794780 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.733-3417A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794780 | |||||||
| chr15:51794793 | A | T | 21 | a0001c0001t0004g0002 a0001c0001t0004g0050 a0001c0001t0004g0054 others(18): Show |
24 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.733-3404A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794793 | |||||||
| chr15:51794806 | A | G | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-3391A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794806 | |||||||
| chr15:51795024 | C | A | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.733-3173C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795024 | |||||||
| chr15:51795080 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.733-3117C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795080 | |||||||
| chr15:51795227 | C | T | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2970C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795227 | |||||||
| chr15:51795229 | T | C | 1 | a0002c0002t0004g0064 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.733-2968T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795229 | |||||||
| chr15:51795250 | G | A | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-2947G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795250 | |||||||
| chr15:51795268 | TA | T | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-2921delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795268 | ||||||
| chr15:51795428 | C | CA | 115 | a0001c0001t0001g0021 a0001c0001t0001g0251 a0001c0001t0001g0252 others(112): Show |
116 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.733-2753dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795428 | ||||||
| chr15:51795428 | CA | C | 53 | a0001c0001t0004g0071 a0001c0001t0005g0016 a0001c0001t0005g0170 others(50): Show |
55 | HG00423.hp2 HG00544.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.733-2753delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795428 | ||||||
| chr15:51795442 | A | AG | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-2755_733-2754i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795442 | |||||||
| chr15:51795466 | G | C | 1 | a0001c0001t0017g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-2731G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795466 | |||||||
| chr15:51795475 | G | C | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2722G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795475 | |||||||
| chr15:51795563 | CTGCT | C | 20 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(17): Show |
21 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.733-2620_733-2617d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795563 | ||||||
| chr15:51795563 | CTGCTTGC others(1): Show |
C | 20 | a0001c0001t0001g0288 a0001c0001t0002g0026 a0001c0001t0002g0119 others(17): Show |
22 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.733-2624_733-2617d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795563 | ||||||
| chr15:51795563 | CTGCTTGC others(5): Show |
C | 26 | a0001c0001t0002g0025 a0001c0001t0005g0016 a0001c0001t0005g0170 others(23): Show |
29 | HG00423.hp2 HG00544.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.733-2628_733-2617d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795563 | ||||||
| chr15:51795565 | GCTTGCTT others(9): Show |
G | 26 | a0001c0001t0002g0024 a0001c0001t0005g0172 a0001c0001t0005g0173 others(23): Show |
26 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.733-2628_733-2613d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795565 | GCTTGCTT others(13): Show |
G | 14 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0084 others(11): Show |
14 | HG00735.hp1 HG01106.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.733-2628_733-2609d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795565 | GCTTGCTT others(17): Show |
G | 18 | a0001c0001t0002g0056 a0001c0001t0002g0099 a0001c0001t0002g0106 others(15): Show |
18 | HG00140.hp1 HG00741.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.733-2628_733-2605d others(26): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795565 | GCTTGCTT others(21): Show |
G | 40 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0049 others(37): Show |
42 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-2628_733-2601d others(30): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795565 | GCTTGCTT others(25): Show |
G | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
20 | HG00408.hp2 HG00741.hp2 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.733-2628_733-2597d others(34): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795565 | GCTTGCTT others(29): Show |
G | 8 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0089 others(5): Show |
11 | HG02451.hp2 HG02523.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.733-2628_733-2593d others(38): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795565 | GCTTGCTT others(33): Show |
G | 5 | a0001c0001t0002g0096 a0001c0001t0002g0123 a0001c0001t0002g0124 others(2): Show |
5 | HG00323.hp1 HG00609.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-2628_733-2589d others(42): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | ||||||
| chr15:51795569 | G | T | 2 | a0001c0001t0006g0033 a0001c0001t0010g0112 |
2 | HG02280.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.733-2628G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795569 | |||||||
| chr15:51795569 | GCTTGCTT others(5): Show |
G | 8 | a0001c0001t0003g0204 a0001c0001t0003g0212 a0001c0001t0003g0224 others(5): Show |
8 | HG01081.hp2 HG01433.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-2624_733-2613d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | ||||||
| chr15:51795569 | GCTTGCTT others(9): Show |
G | 3 | a0001c0001t0007g0198 a0001c0001t0013g0142 a0001c0001t0013g0143 |
3 | HG03540.hp2 NA18747.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.733-2624_733-2609d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | ||||||
| chr15:51795569 | GCTTGCTT others(13): Show |
G | 3 | a0001c0001t0010g0053 a0001c0001t0013g0144 a0001c0001t0013g0145 |
3 | HG02145.hp1 HG04115.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.733-2624_733-2605d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | ||||||
| chr15:51795569 | GCTTGCTT others(17): Show |
G | 4 | a0001c0001t0007g0200 a0001c0001t0007g0216 a0001c0001t0007g0217 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-2624_733-2601d others(26): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | ||||||
| chr15:51795569 | GCTTGCTT others(21): Show |
G | 6 | a0001c0001t0007g0018 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
7 | HG01255.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-2624_733-2597d others(30): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | ||||||
| chr15:51795573 | G | T | 14 | a0001c0001t0002g0027 a0001c0001t0003g0221 a0001c0001t0003g0238 others(11): Show |
14 | HG00738.hp1 HG01081.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.733-2624G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795573 | |||||||
| chr15:51795573 | GCTTGCTT others(1): Show |
G | 5 | a0001c0001t0001g0249 a0001c0001t0003g0205 a0001c0001t0003g0237 others(2): Show |
6 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-2620_733-2613d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | ||||||
| chr15:51795573 | GCTTGCTT others(5): Show |
G | 5 | a0001c0001t0003g0004 a0001c0001t0007g0017 a0001c0001t0007g0207 others(2): Show |
8 | HG01074.hp2 HG01516.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-2620_733-2609d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | ||||||
| chr15:51795573 | GCTTGCTT others(9): Show |
G | 3 | a0001c0001t0007g0208 a0001c0001t0007g0230 a0001c0001t0014g0307 |
3 | HG02970.hp1 NA18522.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.733-2620_733-2605d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | ||||||
| chr15:51795573 | GCTTGCTT others(13): Show |
G | 3 | a0001c0001t0019g0197 a0001c0001t0019g0199 a0001c0001t0019g0201 |
3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.733-2620_733-2601d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | ||||||
| chr15:51795577 | G | GCTTT | 5 | a0001c0001t0001g0284 a0001c0001t0001g0294 a0001c0001t0001g0319 others(2): Show |
5 | NA18612.hp2 NA18980.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-2561_733-2558d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | G | GCTTTCTT others(1): Show |
3 | a0001c0001t0001g0277 a0001c0001t0001g0311 a0001c0001t0001g0343 |
3 | HG02155.hp2 NA18952.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.733-2565_733-2558d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | G | GCTTTCTT others(5): Show |
1 | a0001c0001t0001g0303 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.733-2569_733-2558d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | G | T | 50 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(47): Show |
54 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.733-2620G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795577 | |||||||
| chr15:51795577 | GCTTT | G | 18 | a0001c0001t0001g0251 a0001c0001t0001g0300 a0001c0001t0001g0304 others(15): Show |
18 | HG00609.hp1 HG01109.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.733-2561_733-2558d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | GCTTTCTT others(1): Show |
G | 14 | a0001c0001t0001g0252 a0001c0001t0001g0265 a0001c0001t0001g0295 others(11): Show |
14 | HG00642.hp1 HG01358.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.733-2565_733-2558d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | GCTTTCTT others(5): Show |
G | 4 | a0001c0001t0001g0315 a0001c0001t0001g0330 a0001c0001t0001g0338 others(1): Show |
4 | HG00639.hp1 HG00733.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2569_733-2558d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | GCTTTCTT others(9): Show |
G | 1 | a0001c0001t0025g0345 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.733-2573_733-2558d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795577 | GCTTTCTT others(13): Show |
G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0292 a0001c0001t0001g0329 others(1): Show |
5 | HG00544.hp2 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-2577_733-2558d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | ||||||
| chr15:51795581 | T | G | 4 | a0001c0001t0001g0272 a0001c0001t0001g0323 a0001c0001t0001g0344 others(1): Show |
4 | NA18957.hp2 NA18979.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2616T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795581 | |||||||
| chr15:51795585 | T | G | 4 | a0001c0001t0001g0326 a0001c0001t0018g0257 a0001c0001t0018g0258 others(1): Show |
4 | HG00609.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2612T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795585 | |||||||
| chr15:51795589 | T | G | 1 | a0001c0001t0001g0316 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.733-2608T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795589 | |||||||
| chr15:51795593 | T | G | 2 | a0001c0001t0001g0315 a0001c0001t0001g0338 |
2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.733-2604T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795593 | |||||||
| chr15:51795597 | T | G | 1 | a0001c0001t0025g0345 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.733-2600T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795597 | |||||||
| chr15:51795610 | C | CTTTCT | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02258.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.733-2584_733-2580d others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795610 | ||||||
| chr15:51795610 | C | CTTTCTTT others(2): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.733-2584_733-2576d others(11): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795610 | ||||||
| chr15:51795610 | C | CTTTCTTT others(6): Show |
1 | a0001c0001t0001g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.733-2584_733-2572d others(15): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795610 | ||||||
| chr15:51795636 | T | C | 1 | a0001c0001t0005g0170 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.733-2561T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795636 | |||||||
| chr15:51795678 | C | T | 1 | a0001c0001t0018g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.733-2519C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795678 | |||||||
| chr15:51795679 | A | G | 4 | a0001c0001t0002g0119 a0001c0001t0020g0062 a0001c0001t0020g0113 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2518A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795679 | |||||||
| chr15:51795709 | C | T | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.733-2488C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795709 | |||||||
| chr15:51795713 | A | G | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-2484A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795713 | |||||||
| chr15:51795909 | A | G | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-2288A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795909 | |||||||
| chr15:51795929 | CTTTCTT | C | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2255_733-2250d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795929 | ||||||
| chr15:51796094 | T | TATTTTTG | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-2102_733-2101i others(9): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51796094 | ||||||
| chr15:51796533 | T | C | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-1664T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796533 | |||||||
| chr15:51796569 | C | G | 2 | a0001c0001t0028g0080 a0001c0001t0031g0081 |
2 | HG01496.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.733-1628C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796569 | |||||||
| chr15:51796699 | A | C | 1 | a0001c0001t0003g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.733-1498A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796699 | |||||||
| chr15:51796959 | T | C | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.733-1238T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796959 | |||||||
| chr15:51796971 | G | C | 1 | a0001c0001t0003g0237 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.733-1226G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796971 | |||||||
| chr15:51796991 | C | G | 37 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(34): Show |
38 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.733-1206C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796991 | |||||||
| chr15:51797088 | G | A | 1 | a0001c0001t0017g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-1109G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797088 | |||||||
| chr15:51797114 | A | C | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-1083A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797114 | |||||||
| chr15:51797234 | T | C | 162 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(159): Show |
176 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.733-963T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797234 | |||||||
| chr15:51797261 | C | A | 1 | a0001c0001t0049g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.733-936C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797261 | |||||||
| chr15:51797424 | C | T | 15 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0032 others(12): Show |
16 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-773C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797424 | |||||||
| chr15:51797500 | A | G | 1 | a0001c0001t0028g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.733-697A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797500 | |||||||
| chr15:51797503 | C | T | 37 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(34): Show |
38 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.733-694C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797503 | |||||||
| chr15:51797574 | A | G | 1 | a0001c0001t0001g0341 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.733-623A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797574 | |||||||
| chr15:51797605 | G | A | 30 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(27): Show |
31 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.733-592G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797605 | |||||||
| chr15:51797628 | C | A | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.733-569C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797628 | |||||||
| chr15:51797629 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.733-568C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797629 | |||||||
| chr15:51797630 | G | C | 1 | a0001c0001t0002g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.733-567G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797630 | |||||||
| chr15:51797745 | A | G | 1 | a0001c0001t0042g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.733-452A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797745 | |||||||
| chr15:51797795 | T | A | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-402T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797795 | |||||||
| chr15:51797881 | C | CA | 24 | a0001c0001t0001g0285 a0001c0001t0001g0301 a0001c0001t0002g0060 others(21): Show |
26 | HG00140.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.733-303dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797881 | ||||||
| chr15:51797881 | CA | C | 31 | a0001c0001t0004g0069 a0001c0001t0004g0071 a0001c0001t0005g0016 others(28): Show |
32 | HG00544.hp1 HG01106.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.733-303delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797881 | ||||||
| chr15:51797881 | CAA | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-304_733-303del others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797881 | ||||||
| chr15:51797903 | G | GTT | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-286_733-285dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797903 | ||||||
| chr15:51797993 | T | G | 1 | a0001c0001t0002g0102 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.733-204T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797993 | |||||||
| chr15:51798508 | A | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+168A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798508 | |||||||
| chr15:51798527 | A | G | 1 | a0001c0001t0007g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.876+187A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798527 | |||||||
| chr15:51798684 | T | G | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.876+344T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798684 | |||||||
| chr15:51798970 | G | A | 178 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.876+630G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798970 | |||||||
| chr15:51799022 | C | T | 1 | a0001c0001t0024g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.876+682C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799022 | |||||||
| chr15:51799330 | G | T | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.876+990G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799330 | |||||||
| chr15:51799435 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.876+1095C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799435 | |||||||
| chr15:51799505 | G | C | 3 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0344 |
3 | HG02155.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.876+1165G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799505 | |||||||
| chr15:51799521 | AG | A | 117 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(114): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.876+1182delG | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799521 | |||||||
| chr15:51799588 | G | A | 169 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(166): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.876+1248G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799588 | |||||||
| chr15:51799609 | G | A | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+1269G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799609 | |||||||
| chr15:51799630 | A | ATG | 4 | a0001c0001t0002g0119 a0001c0001t0020g0062 a0001c0001t0020g0113 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+1293_876+1294d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51799630 | ||||||
| chr15:51800124 | C | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+1784C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800124 | |||||||
| chr15:51800246 | T | C | 1 | a0001c0001t0003g0241 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.876+1906T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800246 | |||||||
| chr15:51800396 | T | C | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(168): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.876+2056T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800396 | |||||||
| chr15:51800488 | A | G | 1 | a0001c0001t0010g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.876+2148A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800488 | |||||||
| chr15:51800529 | G | A | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+2189G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800529 | |||||||
| chr15:51800583 | C | A | 3 | a0001c0001t0010g0053 a0001c0001t0010g0114 a0001c0001t0010g0115 |
3 | HG02145.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.876+2243C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800583 | |||||||
| chr15:51800627 | T | G | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+2287T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800627 | |||||||
| chr15:51800755 | GAGTACAA others(6): Show |
G | 1 | a0001c0001t0002g0089 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.876+2419_876+2431d others(15): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51800755 | ||||||
| chr15:51800907 | A | G | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+2567A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800907 | |||||||
| chr15:51801217 | C | CCT | 34 | a0001c0001t0001g0291 a0001c0001t0001g0322 a0001c0001t0002g0001 others(31): Show |
40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.876+2897_876+2898d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | ||||||
| chr15:51801217 | C | CCTCT | 3 | a0001c0001t0002g0168 a0001c0001t0021g0052 a0001c0001t0021g0095 |
3 | HG00609.hp2 HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.876+2895_876+2898d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | ||||||
| chr15:51801217 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.876+2877C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801217 | |||||||
| chr15:51801217 | CCT | C | 21 | a0001c0001t0001g0153 a0001c0001t0001g0284 a0001c0001t0001g0290 others(18): Show |
25 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.876+2897_876+2898d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | ||||||
| chr15:51801217 | CCTCTCT | C | 3 | a0001c0001t0001g0151 a0001c0001t0012g0022 a0001c0001t0012g0134 |
3 | HG01884.hp2 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.876+2893_876+2898d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | ||||||
| chr15:51801225 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.876+2885T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801225 | |||||||
| chr15:51801229 | T | TCA | 6 | a0001c0001t0001g0149 a0001c0001t0009g0015 a0001c0001t0009g0157 others(3): Show |
7 | HG00140.hp2 HG02965.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.876+2890_876+2891i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801229 | ||||||
| chr15:51801229 | T | TCACA | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0009g0162 others(2): Show |
5 | HG02280.hp2 HG03130.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+2890_876+2891i others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801229 | ||||||
| chr15:51801231 | T | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
18 | HG00140.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.876+2891T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801231 | |||||||
| chr15:51801231 | TCTCTCTC others(1): Show |
T | 5 | a0001c0001t0012g0129 a0001c0001t0012g0130 a0001c0001t0012g0131 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+2893_876+2900d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801231 | ||||||
| chr15:51801233 | T | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0148 others(16): Show |
21 | HG00140.hp2 HG02280.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.876+2893T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801233 | |||||||
| chr15:51801233 | T | TCACACAC others(3): Show |
2 | a0001c0001t0010g0115 a0001c0001t0010g0116 |
2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.876+2894_876+2895i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801233 | ||||||
| chr15:51801233 | T | TCACACAC others(5): Show |
2 | a0001c0001t0010g0053 a0001c0001t0010g0112 |
2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.876+2894_876+2895i others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801233 | ||||||
| chr15:51801233 | T | TCACACAC others(7): Show |
1 | a0001c0001t0010g0011 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.876+2894_876+2895i others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801233 | ||||||
| chr15:51801235 | T | A | 30 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0148 others(27): Show |
33 | HG00140.hp2 HG01243.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.876+2895T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801235 | |||||||
| chr15:51801235 | T | TCA | 9 | a0001c0001t0001g0318 a0001c0001t0003g0206 a0001c0001t0003g0222 others(6): Show |
10 | HG00323.hp2 HG00642.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | T | TCACA | 4 | a0001c0001t0003g0224 a0001c0001t0003g0229 a0001c0001t0003g0242 others(1): Show |
4 | HG00735.hp2 HG00738.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | T | TCACACA | 5 | a0001c0001t0003g0226 a0001c0001t0007g0208 a0001c0001t0007g0213 others(2): Show |
5 | HG02647.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | T | TCACACAC others(1): Show |
6 | a0001c0001t0003g0223 a0001c0001t0007g0198 a0001c0001t0007g0200 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | T | TCACACAC others(3): Show |
2 | a0001c0001t0007g0017 a0001c0001t0007g0207 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.876+2896_876+2897i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | T | TCACACAC others(7): Show |
1 | a0001c0001t0007g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.876+2896_876+2897i others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | T | TCACACAC others(9): Show |
1 | a0001c0001t0007g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.876+2896_876+2897i others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | TCTCA | T | 6 | a0001c0001t0007g0230 a0001c0001t0013g0140 a0001c0001t0013g0142 others(3): Show |
6 | HG02970.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+2897_876+2900d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801235 | TCTCACA | T | 3 | a0001c0001t0003g0204 a0001c0001t0003g0238 a0001c0001t0013g0144 |
3 | HG03834.hp2 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.876+2897_876+2902d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | ||||||
| chr15:51801237 | T | A | 71 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0148 others(68): Show |
76 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.876+2897T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801237 | |||||||
| chr15:51801237 | T | TCA | 24 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0300 others(21): Show |
24 | HG00408.hp1 HG01109.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.876+2943_876+2944d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCACA | 3 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0308 |
3 | HG02572.hp1 NA18957.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.876+2941_876+2944d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCACACA | 2 | a0001c0001t0005g0180 a0001c0001t0017g0005 |
3 | HG01167.hp1 HG01169.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.876+2939_876+2944d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCACACAC others(3): Show |
6 | a0001c0001t0001g0014 a0001c0001t0002g0122 a0001c0001t0005g0172 others(3): Show |
7 | HG01123.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2935_876+2944d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCA | 16 | a0001c0001t0002g0009 a0001c0001t0002g0060 a0001c0001t0002g0098 others(13): Show |
17 | HG00408.hp2 HG00738.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCACA | 8 | a0001c0001t0002g0049 a0001c0001t0002g0085 a0001c0001t0002g0092 others(5): Show |
8 | HG01496.hp2 HG02257.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCACAC others(1): Show |
4 | a0001c0001t0002g0056 a0001c0001t0002g0105 a0001c0001t0002g0109 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCACAC others(3): Show |
12 | a0001c0001t0005g0175 a0001c0001t0005g0177 a0001c0001t0005g0178 others(9): Show |
12 | HG01106.hp2 HG01943.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCACAC others(5): Show |
5 | a0001c0001t0002g0083 a0001c0001t0002g0104 a0001c0001t0005g0016 others(2): Show |
6 | HG00544.hp1 HG01433.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCACAC others(7): Show |
1 | a0001c0001t0005g0188 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.876+2898_876+2899i others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCACAC others(9): Show |
1 | a0001c0001t0005g0181 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.876+2898_876+2899i others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | T | TCTCTCAC others(3): Show |
1 | a0001c0001t0002g0087 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.876+2898_876+2899i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | TCA | T | 31 | a0001c0001t0001g0265 a0001c0001t0001g0289 a0001c0001t0001g0332 others(28): Show |
33 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.876+2943_876+2944d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | TCACA | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0292 a0001c0001t0001g0303 others(8): Show |
12 | HG00544.hp2 HG01934.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.876+2941_876+2944d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801237 | TCACACAC others(7): Show |
T | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01109.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+2931_876+2944d others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | ||||||
| chr15:51801239 | A | T | 22 | a0001c0001t0001g0320 a0001c0001t0002g0003 a0001c0001t0002g0058 others(19): Show |
23 | HG00140.hp1 HG00741.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.876+2899A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801239 | |||||||
| chr15:51801241 | A | T | 22 | a0001c0001t0002g0003 a0001c0001t0002g0082 a0001c0001t0002g0096 others(19): Show |
25 | HG00323.hp1 HG00423.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.876+2901A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801241 | |||||||
| chr15:51801275 | A | ACACACAC others(3): Show |
1 | a0001c0001t0016g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.876+2944_876+2945i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801275 | ||||||
| chr15:51801281 | A | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2941A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801281 | |||||||
| chr15:51801283 | A | C | 3 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0040g0040 |
3 | NA18943.hp2 NA18965.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.876+2943A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801283 | |||||||
| chr15:51801283 | A | G | 1 | a0001c0001t0048g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.876+2943A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801283 | |||||||
| chr15:51801283 | A | T | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2943A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801283 | |||||||
| chr15:51801284 | C | CACA | 3 | a0001c0001t0002g0135 a0001c0001t0015g0232 a0001c0001t0035g0023 |
3 | HG00741.hp2 HG01081.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.876+2944_876+2945i others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801284 | |||||||
| chr15:51801284 | C | CTG | 3 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0040g0040 |
3 | NA18943.hp2 NA18965.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.876+2944_876+2945i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801284 | |||||||
| chr15:51801284 | C | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2944C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801284 | |||||||
| chr15:51801285 | C | T | 10 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0012g0022 others(7): Show |
10 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.876+2945C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801285 | |||||||
| chr15:51801288 | G | C | 11 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0006g0045 others(8): Show |
11 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+2948G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801288 | |||||||
| chr15:51801288 | G | GTC | 8 | a0001c0001t0001g0148 a0001c0001t0002g0024 a0001c0001t0002g0025 others(5): Show |
8 | HG01891.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.876+2974_876+2975d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | ||||||
| chr15:51801288 | G | GTCTC | 20 | a0001c0001t0006g0006 a0001c0001t0006g0029 a0001c0001t0006g0030 others(17): Show |
21 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.876+2972_876+2975d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | ||||||
| chr15:51801288 | G | GTCTCTC | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.876+2970_876+2975d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | ||||||
| chr15:51801288 | GTC | G | 91 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(88): Show |
100 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.876+2974_876+2975d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | ||||||
| chr15:51801288 | GTCTC | G | 13 | a0001c0001t0002g0120 a0001c0001t0009g0015 a0001c0001t0009g0158 others(10): Show |
14 | HG02145.hp2 HG03209.hp2 HG03579.hp2 others(11): Show |
intron_variant | MODIFIER | c.876+2972_876+2975d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | ||||||
| chr15:51801316 | A | G | 1 | a0001c0001t0009g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.876+2976A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801316 | |||||||
| chr15:51801380 | G | A | 1 | a0001c0001t0016g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.876+3040G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801380 | |||||||
| chr15:51801591 | G | T | 1 | a0001c0001t0049g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.876+3251G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801591 | |||||||
| chr15:51801655 | G | A | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.876+3315G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801655 | |||||||
| chr15:51801734 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+3394A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801734 | |||||||
| chr15:51801889 | C | T | 118 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(115): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.876+3549C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801889 | |||||||
| chr15:51801914 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+3574A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801914 | |||||||
| chr15:51801918 | C | T | 2 | a0001c0001t0004g0067 a0001c0001t0004g0070 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.876+3578C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801918 | |||||||
| chr15:51801947 | T | TATAAC | 170 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(167): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.876+3612_876+3616d others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801947 | ||||||
| chr15:51801947 | T | TATAACAT others(3): Show |
1 | a0001c0001t0016g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.876+3616_876+3617i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801947 | ||||||
| chr15:51802012 | G | A | 16 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(13): Show |
17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+3672G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802012 | |||||||
| chr15:51802137 | C | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(4): Show |
9 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.876+3797C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802137 | |||||||
| chr15:51802152 | C | T | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.876+3812C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802152 | |||||||
| chr15:51802171 | C | T | 118 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(115): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.876+3831C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802171 | |||||||
| chr15:51802219 | CA | C | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+3888delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51802219 | ||||||
| chr15:51802403 | T | G | 2 | a0001c0001t0003g0004 a0001c0001t0003g0237 |
4 | HG01074.hp2 HG01192.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.877-3974T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802403 | |||||||
| chr15:51802483 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.877-3894G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802483 | |||||||
| chr15:51802545 | G | A | 118 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(115): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.877-3832G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802545 | |||||||
| chr15:51802803 | T | C | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-3574T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802803 | |||||||
| chr15:51802928 | T | C | 118 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(115): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.877-3449T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802928 | |||||||
| chr15:51802981 | A | C | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-3396A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802981 | |||||||
| chr15:51802982 | A | T | 118 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(115): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.877-3395A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802982 | |||||||
| chr15:51803113 | G | A | 1 | a0001c0001t0016g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.877-3264G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803113 | |||||||
| chr15:51803144 | A | AATTAAAT others(3): Show |
7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-3232_877-3223d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51803144 | ||||||
| chr15:51803168 | C | CT | 126 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(123): Show |
131 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.877-3186dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51803168 | ||||||
| chr15:51803184 | T | TC | 92 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(89): Show |
101 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.877-3193_877-3192i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803184 | |||||||
| chr15:51803190 | T | G | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-3187T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803190 | |||||||
| chr15:51803190 | T | TG | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.877-3187_877-3186i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803190 | |||||||
| chr15:51803275 | G | T | 1 | a0001c0001t0008g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.877-3102G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803275 | |||||||
| chr15:51803288 | C | A | 1 | a0001c0001t0053g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.877-3089C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803288 | |||||||
| chr15:51803305 | T | C | 171 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(168): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.877-3072T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803305 | |||||||
| chr15:51803381 | A | G | 1 | a0001c0001t0008g0254 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.877-2996A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803381 | |||||||
| chr15:51803396 | G | T | 1 | a0001c0001t0036g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.877-2981G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803396 | |||||||
| chr15:51803449 | G | A | 3 | a0001c0001t0012g0129 a0001c0001t0012g0132 a0001c0001t0012g0133 |
3 | HG02451.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.877-2928G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803449 | |||||||
| chr15:51803511 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.877-2866C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803511 | |||||||
| chr15:51803625 | A | G | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-2752A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803625 | |||||||
| chr15:51803880 | C | T | 1 | a0001c0001t0005g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.877-2497C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803880 | |||||||
| chr15:51803952 | A | G | 3 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG00642.hp1 HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.877-2425A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803952 | |||||||
| chr15:51804027 | G | A | 1 | a0001c0001t0034g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.877-2350G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804027 | |||||||
| chr15:51804116 | C | T | 1 | a0001c0001t0010g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.877-2261C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804116 | |||||||
| chr15:51804153 | G | T | 2 | a0001c0001t0003g0222 a0001c0001t0003g0224 |
2 | HG01255.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.877-2224G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804153 | |||||||
| chr15:51804181 | G | T | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.877-2196G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804181 | |||||||
| chr15:51804194 | A | T | 2 | a0001c0001t0017g0005 a0001c0001t0017g0146 |
3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.877-2183A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804194 | |||||||
| chr15:51804445 | A | G | 5 | a0001c0001t0007g0017 a0001c0001t0007g0207 a0001c0001t0007g0208 others(2): Show |
6 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-1932A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804445 | |||||||
| chr15:51804460 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1917A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804460 | |||||||
| chr15:51804553 | A | ATGTTT | 10 | a0001c0001t0005g0170 a0001c0001t0005g0175 a0001c0001t0005g0177 others(7): Show |
10 | NA18612.hp1 NA18747.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.877-1824_877-1823i others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804553 | |||||||
| chr15:51804554 | C | T | 26 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(23): Show |
27 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.877-1823C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804554 | |||||||
| chr15:51804554 | CGTTTTGT others(3): Show |
C | 1 | a0001c0001t0002g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.877-1802_877-1793d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51804554 | ||||||
| chr15:51804575 | GTTTTGTT others(3): Show |
G | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.877-1797_877-1788d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51804575 | ||||||
| chr15:51804580 | GTTTTT | G | 13 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(10): Show |
13 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.877-1790_877-1786d others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51804580 | ||||||
| chr15:51804585 | T | G | 33 | a0001c0001t0001g0303 a0001c0001t0001g0318 a0001c0001t0005g0016 others(30): Show |
34 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.877-1792T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804585 | |||||||
| chr15:51804601 | C | T | 287 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(284): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.877-1776C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804601 | |||||||
| chr15:51804665 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(118): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.877-1712C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804665 | |||||||
| chr15:51804683 | C | T | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-1694C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804683 | |||||||
| chr15:51804727 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0033g0003 |
3 | HG02451.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.877-1650C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804727 | |||||||
| chr15:51804814 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(118): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.877-1563G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804814 | |||||||
| chr15:51804896 | G | A | 1 | a0001c0001t0012g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.877-1481G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804896 | |||||||
| chr15:51805055 | T | C | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-1322T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805055 | |||||||
| chr15:51805083 | C | G | 3 | a0001c0001t0016g0137 a0001c0001t0016g0138 a0001c0001t0016g0139 |
3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.877-1294C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805083 | |||||||
| chr15:51805160 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1217A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805160 | |||||||
| chr15:51805179 | C | A | 1 | a0001c0001t0005g0188 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.877-1198C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805179 | |||||||
| chr15:51805192 | T | C | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-1185T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805192 | |||||||
| chr15:51805244 | G | A | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1133G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805244 | |||||||
| chr15:51805272 | A | C | 1 | a0001c0001t0003g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877-1105A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805272 | |||||||
| chr15:51805327 | A | C | 10 | a0001c0001t0009g0015 a0001c0001t0009g0157 a0001c0001t0009g0158 others(7): Show |
11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.877-1050A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805327 | |||||||
| chr15:51805420 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-957A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805420 | |||||||
| chr15:51805683 | T | C | 1 | a0001c0001t0043g0283 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.877-694T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805683 | |||||||
| chr15:51805685 | G | C | 1 | a0001c0001t0007g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.877-692G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805685 | |||||||
| chr15:51805904 | A | G | 1 | a0001c0001t0023g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.877-473A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805904 | |||||||
| chr15:51805932 | T | C | 3 | a0001c0001t0019g0197 a0001c0001t0019g0199 a0001c0001t0019g0201 |
3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.877-445T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805932 | |||||||
| chr15:51806692 | C | T | 1 | a0001c0001t0047g0275 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1021+171C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806692 | |||||||
| chr15:51806704 | T | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(118): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1021+183T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806704 | |||||||
| chr15:51806835 | C | G | 8 | a0001c0001t0009g0015 a0001c0001t0009g0159 a0001c0001t0009g0162 others(5): Show |
9 | NA18946.hp2 NA18957.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1021+314C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806835 | |||||||
| chr15:51806961 | A | G | 27 | a0001c0001t0005g0016 a0001c0001t0005g0170 a0001c0001t0005g0172 others(24): Show |
28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.1021+440A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806961 | |||||||
| chr15:51807433 | C | T | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0018g0257 others(2): Show |
5 | HG01109.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021+912C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807433 | |||||||
| chr15:51807517 | C | T | 4 | a0001c0001t0012g0129 a0001c0001t0012g0132 a0001c0001t0012g0133 others(1): Show |
4 | HG02451.hp1 HG03579.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-903C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807517 | |||||||
| chr15:51807540 | G | A | 1 | a0001c0001t0017g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1022-880G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807540 | |||||||
| chr15:51807562 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0326 a0001c0001t0050g0293 |
3 | HG00609.hp1 HG02523.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1022-858C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807562 | |||||||
| chr15:51807808 | A | G | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-612A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807808 | |||||||
| chr15:51807814 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1022-606G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807814 | |||||||
| chr15:51807865 | C | T | 6 | a0001c0001t0013g0140 a0001c0001t0013g0142 a0001c0001t0013g0143 others(3): Show |
6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-555C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807865 | |||||||
| chr15:51807948 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1022-472A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807948 | |||||||
| chr15:51807949 | G | T | 1 | a0001c0001t0002g0102 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1022-471G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807949 | |||||||
| chr15:51807978 | G | C | 7 | a0001c0001t0012g0022 a0001c0001t0012g0129 a0001c0001t0012g0130 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-442G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807978 | |||||||
| chr15:51808018 | C | T | 6 | a0001c0001t0002g0096 a0001c0001t0002g0107 a0001c0001t0002g0123 others(3): Show |
6 | HG00323.hp1 HG00741.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-402C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808018 | |||||||
| chr15:51808094 | A | G | 172 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(169): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1022-326A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808094 | |||||||
| chr15:51808106 | G | A | 3 | a0001c0001t0002g0082 a0001c0001t0028g0080 a0001c0001t0031g0081 |
3 | HG01496.hp2 HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1022-314G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808106 | |||||||
| chr15:51808223 | A | C | 227 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(224): Show |
239 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1022-197A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808223 |