Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 144404 |
|---|---|
| ensemblid | ENSG00000188735.13 |
| hgncid | 32008 |
| symbol | TMEM120B |
| name | transmembrane protein 120B |
| refseq_nuc | NM_001080825.2 |
| refseq_prot | NP_001074294.2 |
| ensembl_nuc | ENST00000449592.7 |
| ensembl_prot | ENSP00000404991.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 121712752 |
| end | 121782068 |
| strand | + |
| ver | v1.2 |
| region | chr12:121712752-121782068 |
| region5000 | chr12:121707752-121787068 |
| regionname0 | TMEM120B_chr12_121712752_121782068 |
| regionname5000 | TMEM120B_chr12_121707752_121787068 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 339 | 191 | 67 | 29 | 64 | 10 | 19 | 44 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002 | 0/0 | 339 | 110 | 18 | 28 | 45 | 4 | 15 | 26 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0003 | 0/0 | 339 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0004 | 0/0 | 339 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0005 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0006 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1020 | 186 | 62 | 29 | 64 | 10 | 19 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0002 | 0/0 | 1020 | 110 | 18 | 28 | 45 | 4 | 15 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0003 | 0/0 | 1020 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0004 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0005 | 0/0 | 1020 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0006 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0007 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0008 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| c0009 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 6493 | 39 | 1 | 9 | 17 | 3 | 8 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0002 | 0/0 | 6486 | 21 | 9 | 1 | 8 | 0 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0003 | 0/0 | 6493 | 18 | 13 | 4 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0004 | 0/0 | 6493 | 18 | 0 | 4 | 10 | 1 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0005 | 0/0 | 6486 | 12 | 7 | 0 | 2 | 0 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0006 | 0/0 | 6486 | 10 | 0 | 0 | 10 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0007 | 0/0 | 6494 | 9 | 0 | 0 | 7 | 0 | 2 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0008 | 0/0 | 6494 | 8 | 0 | 0 | 8 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0009 | 0/0 | 6494 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0010 | 0/0 | 6487 | 7 | 2 | 1 | 3 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0011 | 0/0 | 6487 | 7 | 1 | 6 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0012 | 1/0 | 6491 | 6 | 4 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0013 | 0/0 | 6493 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0014 | 0/0 | 6494 | 5 | 0 | 4 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0015 | 0/0 | 6495 | 5 | 0 | 0 | 1 | 0 | 4 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0016 | 0/0 | 6486 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0017 | 0/0 | 6493 | 4 | 0 | 3 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0018 | 0/0 | 6494 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0019 | 0/0 | 6486 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0020 | 0/0 | 6486 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0021 | 0/0 | 6486 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0022 | 0/0 | 6493 | 3 | 0 | 1 | 0 | 2 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0023 | 0/0 | 6493 | 3 | 0 | 0 | 0 | 2 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0024 | 0/0 | 6494 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0025 | 0/0 | 6494 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0026 | 0/0 | 6493 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0027 | 0/0 | 6487 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0028 | 0/0 | 6486 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0029 | 0/0 | 6486 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0030 | 0/0 | 6487 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0031 | 0/0 | 6488 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0032 | 0/0 | 6486 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0033 | 0/0 | 6486 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0034 | 0/0 | 6493 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0035 | 0/0 | 6490 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0036 | 0/0 | 6494 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0037 | 0/0 | 6493 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0038 | 0/0 | 6492 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0039 | 0/0 | 6494 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0040 | 0/0 | 6495 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0041 | 0/0 | 6495 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0042 | 0/0 | 6515 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0043 | 0/0 | 6494 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0044 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0045 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0046 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0047 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0048 | 0/0 | 6492 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0049 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0050 | 0/0 | 6486 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0051 | 0/0 | 6488 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0052 | 0/0 | 6485 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0053 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0054 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0055 | 0/0 | 6487 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0056 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0057 | 0/0 | 6486 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0058 | 0/0 | 6486 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0059 | 0/0 | 6485 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0060 | 0/0 | 6486 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0061 | 0/0 | 6486 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0062 | 0/0 | 6485 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0063 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0064 | 0/0 | 6486 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0065 | 0/0 | 6486 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0066 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0067 | 0/0 | 6486 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0068 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0069 | 0/0 | 6488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0070 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0071 | 0/0 | 6487 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0072 | 0/0 | 6489 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0073 | 0/0 | 6488 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0074 | 0/0 | 6487 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0075 | 0/0 | 6487 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0076 | 0/0 | 6495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0077 | 0/0 | 6493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0078 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0079 | 0/0 | 6492 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0080 | 0/0 | 6492 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0081 | 0/0 | 6492 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0082 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0083 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0084 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0085 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0086 | 0/0 | 6492 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0087 | 0/0 | 6494 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0088 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0089 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0090 | 0/0 | 6493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0091 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0092 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0093 | 0/0 | 6492 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0094 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0095 | 0/0 | 6495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0096 | 0/0 | 6494 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0097 | 0/0 | 6494 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0098 | 0/0 | 6494 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0099 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0100 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0101 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0102 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0103 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0104 | 0/0 | 6492 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0105 | 0/0 | 6494 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0106 | 0/0 | 6496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0107 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0108 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0109 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0110 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| t0111 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1020 | 186 | 62 | 29 | 64 | 10 | 19 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0004 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0007 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0009 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002 | 0/0 | 1020 | 110 | 18 | 28 | 45 | 4 | 15 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0003c0003 | 0/0 | 1020 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0004c0005 | 0/0 | 1020 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0005c0006 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0006c0008 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7512 | 17 | 1 | 2 | 8 | 1 | 4 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0002 | 0/0 | 7505 | 13 | 5 | 0 | 5 | 0 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0003 | 0/0 | 7512 | 12 | 7 | 4 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0004 | 0/0 | 7512 | 6 | 0 | 3 | 2 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0005 | 0/0 | 7505 | 12 | 7 | 0 | 2 | 0 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0006 | 0/0 | 7505 | 10 | 0 | 0 | 10 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0007 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0008 | 0/0 | 7513 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0009 | 0/0 | 7513 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0010 | 0/0 | 7506 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0011 | 0/0 | 7506 | 7 | 1 | 6 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0012 | 1/0 | 7510 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0013 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0015 | 0/0 | 7514 | 4 | 0 | 0 | 1 | 0 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0016 | 0/0 | 7505 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0017 | 0/0 | 7512 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0018 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0019 | 0/0 | 7505 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0020 | 0/0 | 7505 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0021 | 0/0 | 7505 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0022 | 0/0 | 7512 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0023 | 0/0 | 7512 | 3 | 0 | 0 | 0 | 2 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0025 | 0/0 | 7513 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0026 | 0/0 | 7512 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0027 | 0/0 | 7506 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0028 | 0/0 | 7505 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0029 | 0/0 | 7505 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0030 | 0/0 | 7506 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0032 | 0/0 | 7505 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0033 | 0/0 | 7505 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0035 | 0/0 | 7509 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0036 | 0/0 | 7513 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0037 | 0/0 | 7512 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0040 | 0/0 | 7514 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0041 | 0/0 | 7514 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0042 | 0/0 | 7534 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0043 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0044 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0046 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0049 | 0/0 | 7506 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0050 | 0/0 | 7505 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0051 | 0/0 | 7507 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0052 | 0/0 | 7504 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0054 | 0/0 | 7506 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0055 | 0/0 | 7506 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0056 | 0/0 | 7506 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0057 | 0/0 | 7505 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0059 | 0/0 | 7504 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0060 | 0/0 | 7505 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0062 | 0/0 | 7504 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0063 | 0/0 | 7506 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0066 | 0/0 | 7506 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0067 | 0/0 | 7505 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0069 | 0/0 | 7507 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0070 | 0/0 | 7506 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0071 | 0/0 | 7506 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0072 | 0/0 | 7508 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0074 | 0/0 | 7506 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0075 | 0/0 | 7506 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0076 | 0/0 | 7514 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0078 | 0/0 | 7510 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0079 | 0/0 | 7511 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0080 | 0/0 | 7511 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0081 | 0/0 | 7511 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0082 | 0/0 | 7511 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0083 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0084 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0087 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0090 | 0/0 | 7512 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0092 | 0/0 | 7512 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0097 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0101 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0102 | 0/0 | 7499 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0103 | 0/0 | 7512 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0106 | 0/0 | 7515 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0107 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0108 | 0/0 | 7510 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0109 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0110 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0001t0111 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0004t0003 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0004t0099 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0004t0100 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0007t0026 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0001c0009t0018 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0001 | 0/0 | 7512 | 22 | 0 | 7 | 9 | 2 | 4 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0002 | 0/0 | 7505 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0003 | 0/0 | 7512 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0004 | 0/0 | 7512 | 11 | 0 | 1 | 7 | 0 | 3 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0007 | 0/0 | 7513 | 8 | 0 | 0 | 6 | 0 | 2 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0008 | 0/0 | 7513 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0009 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0010 | 0/0 | 7506 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0012 | 0/0 | 7510 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0013 | 0/0 | 7512 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0014 | 0/0 | 7513 | 5 | 0 | 4 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0015 | 0/0 | 7514 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0016 | 0/0 | 7505 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0017 | 0/0 | 7512 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0018 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0022 | 0/0 | 7512 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0024 | 0/0 | 7513 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0031 | 0/0 | 7507 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0034 | 0/0 | 7512 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0037 | 0/0 | 7512 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0038 | 0/0 | 7511 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0039 | 0/0 | 7513 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0045 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0048 | 0/0 | 7511 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0053 | 0/0 | 7506 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0058 | 0/0 | 7505 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0065 | 0/0 | 7505 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0068 | 0/0 | 7506 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0077 | 0/0 | 7512 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0085 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0086 | 0/0 | 7511 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0088 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0089 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0091 | 0/0 | 7510 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0093 | 0/0 | 7511 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0094 | 0/0 | 7512 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0095 | 0/0 | 7514 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0096 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0098 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0104 | 0/0 | 7511 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0002c0002t0105 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0003c0003t0002 | 0/0 | 7505 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0003c0003t0009 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0003c0003t0010 | 0/0 | 7506 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0003c0003t0061 | 0/0 | 7505 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0004c0005t0004 | 0/0 | 7512 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0004c0005t0064 | 0/0 | 7505 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0004c0005t0073 | 0/0 | 7507 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0005c0006t0047 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| a0006c0008t0002 | 0/0 | 7505 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | copy fasta | chr12 | 121707752 | 121787068 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0008g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0011g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0012g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0013g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0015g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0015g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0015g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0015g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0016g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0017g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0019g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0019g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0019g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0020g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0021g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0021g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0021g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0022g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0023g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0023g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0023g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0025g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0025g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0025g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0026g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0026g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0027g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0027g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0028g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0028g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0029g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0029g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0030g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0030g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0032g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0032g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0033g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0033g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0035g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0035g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0036g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0036g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0037g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0040g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0040g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0041g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0041g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0042g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0042g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0043g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0044g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0046g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0049g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0050g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0051g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0052g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0054g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0055g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0056g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0057g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0059g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0060g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0062g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0063g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0066g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0067g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0069g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0070g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0071g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0072g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0074g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0075g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0076g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0078g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0079g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0080g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0081g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0082g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0083g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0084g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0087g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0090g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0092g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0097g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0101g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0102g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0103g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0106g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0107g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0108g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0109g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0110g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0001t0111g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0004t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0004t0099g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0004t0100g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0007t0026g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0001c0009t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0008g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0008g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0008g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0010g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0013g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0013g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0013g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0013g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0014g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0014g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0014g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0014g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0014g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0015g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0017g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0017g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0017g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0022g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0022g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0024g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0024g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0024g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0031g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0031g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0034g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0037g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0038g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0038g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0039g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0039g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0045g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0048g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0053g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0058g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0065g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0068g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0077g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0085g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0086g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0088g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0089g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0091g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0093g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0094g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0095g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0096g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0098g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0104g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0002c0002t0105g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0003c0003t0061g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0004c0005t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0004c0005t0064g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0004c0005t0073g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0005c0006t0047g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| a0006c0008t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0247 | EUR | GBR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00140 | hp2 | a0001 | c0001 | t0030 | g0162 | EUR | GBR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0209 | EUR | FIN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0041 | EUR | FIN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0199 | EUR | FIN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00323 | hp2 | a0001 | c0001 | t0103 | g0296 | EUR | FIN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00423 | hp1 | a0001 | c0001 | t0056 | g0047 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00438 | hp1 | a0002 | c0002 | t0010 | g0161 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00438 | hp2 | a0002 | c0002 | t0007 | g0166 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00544 | hp1 | a0002 | c0002 | t0045 | g0043 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00544 | hp2 | a0001 | c0001 | t0083 | g0114 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00558 | hp1 | a0001 | c0001 | t0032 | g0141 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00597 | hp1 | a0002 | c0002 | t0095 | g0245 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00597 | hp2 | a0002 | c0002 | t0068 | g0231 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0169 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00642 | hp1 | a0001 | c0001 | t0012 | g0074 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00673 | hp1 | a0002 | c0002 | t0004 | g0242 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | CHS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00735 | hp1 | a0002 | c0002 | t0048 | g0089 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00735 | hp2 | a0002 | c0002 | t0024 | g0197 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00738 | hp1 | a0001 | c0001 | t0074 | g0299 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG00741 | hp2 | a0002 | c0002 | t0017 | g0279 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01071 | hp2 | a0002 | c0002 | t0014 | g0196 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0032 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01109 | hp1 | a0002 | c0002 | t0098 | g0190 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01167 | hp1 | a0001 | c0001 | t0020 | g0125 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01167 | hp2 | a0002 | c0002 | t0022 | g0304 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01169 | hp1 | a0001 | c0001 | t0020 | g0126 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01169 | hp2 | a0001 | c0001 | t0080 | g0150 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0274 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01243 | hp2 | a0001 | c0001 | t0076 | g0287 | AMR | PUR | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01255 | hp1 | a0002 | c0002 | t0014 | g0198 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01255 | hp2 | a0001 | c0001 | t0020 | g0122 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01257 | hp1 | a0002 | c0002 | t0017 | g0088 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01257 | hp2 | a0002 | c0002 | t0034 | g0001 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01258 | hp1 | a0002 | c0002 | t0034 | g0001 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01258 | hp2 | a0002 | c0002 | t0039 | g0111 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01261 | hp1 | a0002 | c0002 | t0024 | g0211 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01261 | hp2 | a0001 | c0001 | t0036 | g0123 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01346 | hp2 | a0002 | c0002 | t0024 | g0207 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01358 | hp2 | a0002 | c0002 | t0004 | g0090 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0110 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01433 | hp2 | a0002 | c0002 | t0077 | g0257 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01496 | hp1 | a0002 | c0002 | t0014 | g0228 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01496 | hp2 | a0002 | c0002 | t0039 | g0302 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01516 | hp1 | a0002 | c0002 | t0022 | g0219 | EUR | IBS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01517 | hp1 | a0001 | c0001 | t0081 | g0108 | EUR | IBS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01517 | hp2 | a0001 | c0001 | t0023 | g0298 | EUR | IBS | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0308 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01884 | hp2 | a0003 | c0003 | t0061 | g0071 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01891 | hp1 | a0001 | c0001 | t0060 | g0167 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01928 | hp1 | a0001 | c0001 | t0072 | g0100 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01928 | hp2 | a0002 | c0002 | t0031 | g0091 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0119 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01934 | hp2 | a0001 | c0001 | t0017 | g0295 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01943 | hp1 | a0002 | c0002 | t0093 | g0212 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0217 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01975 | hp2 | a0001 | c0001 | t0075 | g0181 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0263 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01978 | hp2 | a0001 | c0001 | t0011 | g0280 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02004 | hp1 | a0002 | c0002 | t0014 | g0227 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02004 | hp2 | a0001 | c0001 | t0025 | g0265 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02027 | hp1 | a0002 | c0002 | t0089 | g0244 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02027 | hp2 | a0001 | c0001 | t0032 | g0142 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02055 | hp1 | a0001 | c0001 | t0070 | g0063 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0278 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0052 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02071 | hp1 | a0001 | c0001 | t0066 | g0138 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02074 | hp2 | a0001 | c0001 | t0106 | g0048 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02080 | hp2 | a0002 | c0002 | t0007 | g0178 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02129 | hp1 | a0001 | c0001 | t0028 | g0241 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02129 | hp2 | a0002 | c0002 | t0105 | g0097 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02132 | hp2 | a0001 | c0001 | t0028 | g0240 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0051 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02135 | hp2 | a0001 | c0001 | t0025 | g0271 | EAS | KHV | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02145 | hp1 | a0001 | c0001 | t0021 | g0013 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02145 | hp2 | a0001 | c0001 | t0026 | g0016 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02148 | hp1 | a0002 | c0002 | t0031 | g0303 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02155 | hp1 | a0002 | c0002 | t0008 | g0221 | EAS | CDX | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02155 | hp2 | a0004 | c0005 | t0004 | g0130 | EAS | CDX | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02165 | hp1 | a0001 | c0001 | t0107 | g0307 | EAS | CDX | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | CDX | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0011 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02258 | hp2 | a0001 | c0001 | t0040 | g0259 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02280 | hp1 | a0001 | c0001 | t0057 | g0018 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02280 | hp2 | a0001 | c0009 | t0018 | g0131 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02293 | hp2 | a0001 | c0001 | t0011 | g0206 | AMR | PEL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02451 | hp1 | a0001 | c0001 | t0051 | g0154 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02451 | hp2 | a0002 | c0002 | t0016 | g0009 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02572 | hp2 | a0001 | c0001 | t0042 | g0250 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02602 | hp1 | a0002 | c0002 | t0096 | g0215 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02602 | hp2 | a0001 | c0001 | t0023 | g0301 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02615 | hp1 | a0003 | c0003 | t0010 | g0068 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02615 | hp2 | a0001 | c0001 | t0040 | g0260 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02622 | hp1 | a0002 | c0002 | t0094 | g0157 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02622 | hp2 | a0001 | c0001 | t0079 | g0065 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0140 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02630 | hp2 | a0003 | c0003 | t0010 | g0072 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02683 | hp1 | a0002 | c0002 | t0037 | g0208 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02683 | hp2 | a0001 | c0001 | t0071 | g0173 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0171 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02698 | hp2 | a0001 | c0001 | t0015 | g0101 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02717 | hp1 | a0005 | c0006 | t0047 | g0144 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02717 | hp2 | a0001 | c0001 | t0108 | g0156 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02723 | hp2 | a0001 | c0001 | t0102 | g0083 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02738 | hp1 | a0001 | c0001 | t0030 | g0159 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02738 | hp2 | a0001 | c0001 | t0055 | g0095 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02809 | hp2 | a0001 | c0004 | t0100 | g0082 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0087 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02895 | hp1 | a0001 | c0001 | t0042 | g0252 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02895 | hp2 | a0001 | c0001 | t0033 | g0145 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02896 | hp2 | a0001 | c0001 | t0018 | g0024 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02897 | hp2 | a0001 | c0001 | t0033 | g0135 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02922 | hp1 | a0002 | c0002 | t0012 | g0174 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0061 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02965 | hp1 | a0002 | c0002 | t0012 | g0175 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02970 | hp1 | a0001 | c0001 | t0063 | g0062 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02970 | hp2 | a0001 | c0001 | t0054 | g0093 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0289 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02976 | hp2 | a0003 | c0003 | t0002 | g0285 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03041 | hp2 | a0002 | c0002 | t0012 | g0163 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03098 | hp1 | a0001 | c0001 | t0049 | g0158 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03130 | hp1 | a0002 | c0002 | t0018 | g0086 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03130 | hp2 | a0002 | c0002 | t0012 | g0080 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03139 | hp1 | a0001 | c0001 | t0050 | g0155 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03139 | hp2 | a0002 | c0002 | t0009 | g0058 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03195 | hp1 | a0001 | c0001 | t0035 | g0134 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03195 | hp2 | a0001 | c0001 | t0029 | g0076 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03209 | hp1 | a0001 | c0007 | t0026 | g0017 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03209 | hp2 | a0003 | c0003 | t0009 | g0070 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03225 | hp2 | a0003 | c0003 | t0002 | g0069 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03239 | hp2 | a0002 | c0002 | t0065 | g0275 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03453 | hp1 | a0002 | c0002 | t0053 | g0064 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0288 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03486 | hp1 | a0003 | c0003 | t0002 | g0284 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03486 | hp2 | a0001 | c0001 | t0026 | g0015 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03491 | hp2 | a0002 | c0002 | t0004 | g0204 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03516 | hp1 | a0001 | c0001 | t0110 | g0014 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03516 | hp2 | a0002 | c0002 | t0086 | g0291 | AFR | ESN | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03540 | hp1 | a0001 | c0001 | t0046 | g0067 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03540 | hp2 | a0002 | c0002 | t0091 | g0283 | AFR | GWD | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03579 | hp1 | a0002 | c0002 | t0016 | g0286 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03654 | hp1 | a0002 | c0002 | t0058 | g0183 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03654 | hp2 | a0001 | c0001 | t0092 | g0124 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03688 | hp1 | a0001 | c0001 | t0015 | g0096 | SAS | STU | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | STU | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03710 | hp1 | a0002 | c0002 | t0004 | g0210 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03831 | hp1 | a0002 | c0002 | t0007 | g0191 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03831 | hp2 | a0001 | c0001 | t0037 | g0094 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03834 | hp1 | a0002 | c0002 | t0004 | g0187 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03927 | hp2 | a0002 | c0002 | t0007 | g0186 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG04184 | hp1 | a0002 | c0002 | t0010 | g0188 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | BEB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG04199 | hp1 | a0002 | c0002 | t0015 | g0306 | SAS | STU | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0106 | SAS | STU | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | STU | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG04228 | hp2 | a0001 | c0001 | t0015 | g0116 | SAS | STU | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | YRI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | YRI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | CHB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18906 | hp1 | a0001 | c0001 | t0109 | g0182 | AFR | YRI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | YRI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18942 | hp1 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18942 | hp2 | a0001 | c0001 | t0101 | g0007 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18944 | hp1 | a0001 | c0001 | t0087 | g0164 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18944 | hp2 | a0002 | c0002 | t0007 | g0202 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18948 | hp1 | a0002 | c0002 | t0038 | g0216 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18950 | hp1 | a0001 | c0001 | t0025 | g0264 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18951 | hp1 | a0004 | c0005 | t0064 | g0282 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18951 | hp2 | a0002 | c0002 | t0085 | g0205 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18956 | hp1 | a0002 | c0002 | t0013 | g0037 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18960 | hp1 | a0001 | c0001 | t0019 | g0029 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18961 | hp2 | a0002 | c0002 | t0014 | g0127 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18966 | hp2 | a0001 | c0001 | t0010 | g0031 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18969 | hp1 | a0001 | c0001 | t0062 | g0027 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18969 | hp2 | a0001 | c0001 | t0059 | g0137 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0224 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18973 | hp1 | a0002 | c0002 | t0088 | g0160 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18973 | hp2 | a0001 | c0001 | t0027 | g0273 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18980 | hp1 | a0001 | c0001 | t0013 | g0168 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18990 | hp2 | a0002 | c0002 | t0004 | g0103 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18994 | hp1 | a0001 | c0001 | t0019 | g0053 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18994 | hp2 | a0001 | c0001 | t0027 | g0066 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18999 | hp2 | a0002 | c0002 | t0007 | g0200 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19003 | hp1 | a0002 | c0002 | t0008 | g0223 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19004 | hp1 | a0001 | c0001 | t0015 | g0269 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19004 | hp2 | a0001 | c0001 | t0052 | g0054 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0246 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19005 | hp2 | a0002 | c0002 | t0008 | g0309 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19007 | hp1 | a0002 | c0002 | t0013 | g0038 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19007 | hp2 | a0001 | c0001 | t0067 | g0046 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19010 | hp1 | a0002 | c0002 | t0007 | g0235 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19010 | hp2 | a0001 | c0001 | t0041 | g0261 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | LWK | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19030 | hp2 | a0001 | c0001 | t0078 | g0132 | AFR | LWK | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19043 | hp1 | a0001 | c0001 | t0111 | g0078 | AFR | LWK | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | LWK | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19054 | hp1 | a0001 | c0001 | t0097 | g0311 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19054 | hp2 | a0002 | c0002 | t0008 | g0292 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19060 | hp1 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19060 | hp2 | a0001 | c0001 | t0041 | g0262 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19070 | hp1 | a0002 | c0002 | t0013 | g0036 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19070 | hp2 | a0002 | c0002 | t0007 | g0220 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19074 | hp1 | a0001 | c0001 | t0019 | g0034 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19074 | hp2 | a0001 | c0001 | t0008 | g0115 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19084 | hp1 | a0002 | c0002 | t0008 | g0293 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19084 | hp2 | a0001 | c0001 | t0043 | g0310 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19085 | hp1 | a0001 | c0001 | t0044 | g0312 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19085 | hp2 | a0002 | c0002 | t0004 | g0218 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19088 | hp1 | a0002 | c0002 | t0004 | g0229 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19090 | hp1 | a0004 | c0005 | t0073 | g0281 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19090 | hp2 | a0001 | c0001 | t0069 | g0019 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19091 | hp2 | a0002 | c0002 | t0038 | g0230 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | YRI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA19240 | hp2 | a0001 | c0004 | t0099 | g0010 | AFR | YRI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20129 | hp1 | a0002 | c0002 | t0104 | g0165 | AFR | ASW | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20752 | hp1 | a0001 | c0001 | t0036 | g0121 | EUR | TSI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20752 | hp2 | a0002 | c0002 | t0017 | g0258 | EUR | TSI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20805 | hp1 | a0001 | c0001 | t0022 | g0098 | EUR | TSI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20805 | hp2 | a0001 | c0001 | t0023 | g0297 | EUR | TSI | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0305 | SAS | GIH | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | GIH | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01123 | hp1 | a0001 | c0001 | t0090 | g0294 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | CLM | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02486 | hp1 | a0001 | c0001 | t0029 | g0077 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02559 | hp1 | a0001 | c0001 | t0035 | g0133 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG02559 | hp2 | a0006 | c0008 | t0002 | g0143 | AFR | ACB | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0085 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0290 | AFR | MSL | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | USA | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | USA | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18955 | hp1 | a0002 | c0002 | t0013 | g0039 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA18955 | hp2 | a0001 | c0001 | t0082 | g0073 | EAS | JPT | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0102 | AFR | USA | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | USA | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA21309 | hp1 | a0001 | c0001 | t0084 | g0146 | AFR | LWK | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | LWK | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0105 | REF | REF | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0153 | REF | REF | TMEM120B_chr12_121707752_121787068 | TMEM120B | chr12 | 121707752 | 121787068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121712954
|
A | C | 1 | a0004 | 3 | HG02155.hp2 NA18951.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.59A>C | p.Gln20Pro | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/12 | 203/7510 | 59/1020 | 20/339 | chr12 | 121712954 | ||
| chr12:121748333
|
C | T | 1 | a0003 | 8 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(5): Show |
missense_variant | MODERATE | c.196C>T | p.Arg66Cys | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/12 | 340/7510 | 196/1020 | 66/339 | chr12 | 121748333 | ||
| chr12:121748334
|
G | A | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.197G>A | p.Arg66His | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/12 | 341/7510 | 197/1020 | 66/339 | chr12 | 121748334 | ||
| chr12:121748411
|
G | A | 1 | a0002 | 110 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
missense_variant | MODERATE | c.274G>A | p.Asp92Asn | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/12 | 418/7510 | 274/1020 | 92/339 | chr12 | 121748411 | ||
| chr12:121770957
|
G | C | 1 | a0006 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.602G>C | p.Gly201Ala | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/12 | 746/7510 | 602/1020 | 201/339 | chr12 | 121770957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121748362
|
C | T | 1 | a0002c0002 | 110 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
synonymous_variant | LOW | c.225C>T | p.Leu75Leu | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/12 | 369/7510 | 225/1020 | 75/339 | chr12 | 121748362 | ||
| chr12:121748380
|
G | A | 1 | a0001c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.243G>A | p.Ala81Ala | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/12 | 387/7510 | 243/1020 | 81/339 | chr12 | 121748380 | ||
| chr12:121761730
|
C | T | 1 | a0001c0004 | 3 | HG02809.hp1 HG02809.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.543C>T | p.Asn181Asn | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/12 | 687/7510 | 543/1020 | 181/339 | chr12 | 121761730 | ||
| chr12:121775082
|
C | G | 1 | a0001c0009 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.858C>G | p.Ala286Ala | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/12 | 1002/7510 | 858/1020 | 286/339 | chr12 | 121775082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121712833
|
G | GGGGGCCG others(15): Show |
1 | a0001c0001t0042 | 2 | HG02572.hp2 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-59_-38dupGCCGGTCG others(14): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/12 | 37 | INFO_REALIGN_3_PRIME | chr12 | 121712833 | ||||
| chr12:121775804
|
G | C | 3 | a0001c0001t0043a0001c0001t0044a0002c0002t0045 | 3 | HG00544.hp1 NA19084.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*82G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 82 | chr12 | 121775804 | |||||
| chr12:121775843
|
G | A | 2 | a0001c0001t0043a0001c0001t0044 | 2 | NA19084.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*121G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 121 | chr12 | 121775843 | |||||
| chr12:121775993
|
T | C | 5 | a0001c0001t0009a0001c0001t0046a0002c0002t0009others(2): Show | 9 | HG02109.hp1 HG02486.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*271T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 271 | chr12 | 121775993 | |||||
| chr12:121776207
|
G | A | 1 | a0002c0002t0048 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 485 | chr12 | 121776207 | |||||
| chr12:121776256
|
CGCGTCT | C | 49 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(46): Show | 111 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*537_*542delGTCTGC | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 537 | INFO_REALIGN_3_PRIME | chr12 | 121776256 | ||||
| chr12:121776267
|
C | T | 1 | a0001c0001t0111 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 545 | chr12 | 121776267 | |||||
| chr12:121776268
|
G | A | 6 | a0001c0001t0009a0001c0001t0046a0001c0001t0076others(3): Show | 11 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*546G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 546 | chr12 | 121776268 | |||||
| chr12:121776284
|
T | TG | 22 | a0001c0001t0009a0001c0001t0015a0001c0001t0018others(19): Show | 40 | HG01071.hp2 HG01243.hp2 HG01255.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*564dupG | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 565 | INFO_REALIGN_3_PRIME | chr12 | 121776284 | ||||
| chr12:121776327
|
C | T | 3 | a0001c0001t0026a0001c0001t0110a0001c0007t0026 | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 605 | chr12 | 121776327 | |||||
| chr12:121776373
|
C | T | 1 | a0001c0001t0109 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*651C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 651 | chr12 | 121776373 | |||||
| chr12:121776380
|
G | A | 2 | a0002c0002t0014a0002c0002t0077 | 6 | HG01071.hp2 HG01255.hp1 HG01433.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*658G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 658 | chr12 | 121776380 | |||||
| chr12:121776399
|
C | G | 1 | a0001c0001t0075 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 677 | chr12 | 121776399 | |||||
| chr12:121776408
|
C | G | 1 | a0001c0001t0033 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*686C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 686 | chr12 | 121776408 | |||||
| chr12:121776500
|
C | G | 1 | a0001c0001t0032 | 2 | HG00558.hp1 HG02027.hp2 |
3_prime_UTR_variant | MODIFIER | c.*778C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 778 | chr12 | 121776500 | |||||
| chr12:121776701
|
C | G | 1 | a0001c0001t0107 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 979 | chr12 | 121776701 | |||||
| chr12:121776801
|
C | CT | 4 | a0001c0001t0106a0002c0002t0024a0002c0002t0104others(1): Show | 6 | HG00735.hp2 HG01261.hp1 HG01346.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1092dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1093 | INFO_REALIGN_3_PRIME | chr12 | 121776801 | ||||
| chr12:121776801
|
CT | C | 52 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(49): Show | 108 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1092delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1092 | INFO_REALIGN_3_PRIME | chr12 | 121776801 | ||||
| chr12:121776856
|
T | C | 2 | a0001c0001t0043a0001c0001t0044 | 2 | NA19084.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1134T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1134 | chr12 | 121776856 | |||||
| chr12:121776873
|
C | T | 3 | a0001c0001t0023a0001c0001t0074a0001c0001t0103 | 5 | HG00323.hp2 HG00738.hp1 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1151C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1151 | chr12 | 121776873 | |||||
| chr12:121776923
|
GACCACAA others(6): Show |
G | 1 | a0001c0001t0102 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1207_*1219delAATC others(9): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1207 | INFO_REALIGN_3_PRIME | chr12 | 121776923 | ||||
| chr12:121776930
|
A | G | 45 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(42): Show | 100 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1208A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1208 | chr12 | 121776930 | |||||
| chr12:121776935
|
A | G | 2 | a0001c0001t0029a0001c0001t0070 | 3 | HG02055.hp1 HG02486.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1213A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1213 | chr12 | 121776935 | |||||
| chr12:121776954
|
C | CT | 13 | a0001c0001t0008a0001c0001t0015a0001c0001t0040others(10): Show | 24 | HG00597.hp1 HG00621.hp2 HG01109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1250dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1251 | INFO_REALIGN_3_PRIME | chr12 | 121776954 | ||||
| chr12:121776954
|
CT | C | 6 | a0001c0001t0043a0001c0001t0044a0001c0001t0069others(3): Show | 6 | HG00597.hp2 HG00735.hp1 HG01517.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1250delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1250 | INFO_REALIGN_3_PRIME | chr12 | 121776954 | ||||
| chr12:121776954
|
CTT | C | 48 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(45): Show | 104 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1250delTT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1249 | INFO_REALIGN_3_PRIME | chr12 | 121776954 | ||||
| chr12:121777102
|
C | T | 2 | a0001c0001t0066a0001c0001t0067 | 2 | HG02071.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1380C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1380 | chr12 | 121777102 | |||||
| chr12:121777117
|
G | A | 53 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(50): Show | 109 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1395G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1395 | chr12 | 121777117 | |||||
| chr12:121777155
|
A | G | 1 | a0002c0002t0065 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1433A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1433 | chr12 | 121777155 | |||||
| chr12:121777222
|
A | G | 50 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(47): Show | 94 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1500A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1500 | chr12 | 121777222 | |||||
| chr12:121777290
|
T | A | 52 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(49): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1568T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1568 | chr12 | 121777290 | |||||
| chr12:121777353
|
C | T | 49 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(46): Show | 102 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1631C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1631 | chr12 | 121777353 | |||||
| chr12:121777450
|
A | C | 2 | a0004c0005t0064a0004c0005t0073 | 2 | NA18951.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1728A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1728 | chr12 | 121777450 | |||||
| chr12:121777518
|
G | A | 1 | a0001c0001t0082 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1796 | chr12 | 121777518 | |||||
| chr12:121777535
|
C | G | 2 | a0001c0001t0022a0002c0002t0022 | 3 | HG01167.hp2 HG01516.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1813C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1813 | chr12 | 121777535 | |||||
| chr12:121777614
|
T | C | 62 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(59): Show | 127 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1892T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1892 | chr12 | 121777614 | |||||
| chr12:121777651
|
G | T | 1 | a0001c0001t0041 | 2 | NA19010.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1929G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1929 | chr12 | 121777651 | |||||
| chr12:121777700
|
G | A | 1 | a0001c0001t0083 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1978G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1978 | chr12 | 121777700 | |||||
| chr12:121777720
|
C | A | 82 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(79): Show | 173 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1998C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 1998 | chr12 | 121777720 | |||||
| chr12:121777865
|
C | T | 3 | a0001c0001t0049a0001c0001t0050a0001c0001t0051 | 3 | HG02451.hp1 HG03098.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2143C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2143 | chr12 | 121777865 | |||||
| chr12:121777901
|
C | T | 6 | a0001c0001t0009a0001c0001t0046a0001c0001t0076others(3): Show | 11 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2179C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2179 | chr12 | 121777901 | |||||
| chr12:121777950
|
C | T | 19 | a0001c0001t0002a0001c0001t0006a0001c0001t0010others(16): Show | 55 | HG00438.hp1 HG00597.hp2 HG01099.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2228C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2228 | chr12 | 121777950 | |||||
| chr12:121778080
|
A | C | 1 | a0002c0002t0094 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2358A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2358 | chr12 | 121778080 | |||||
| chr12:121778130
|
A | G | 52 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(49): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2408A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2408 | chr12 | 121778130 | |||||
| chr12:121778136
|
C | T | 2 | a0001c0001t0043a0001c0001t0044 | 2 | NA19084.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2414C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2414 | chr12 | 121778136 | |||||
| chr12:121778190
|
C | T | 1 | a0001c0004t0100 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2468C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2468 | chr12 | 121778190 | |||||
| chr12:121778235
|
G | A | 2 | a0001c0001t0035a0001c0001t0078 | 3 | HG02559.hp1 HG03195.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2513G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2513 | chr12 | 121778235 | |||||
| chr12:121778261
|
G | A | 1 | a0002c0002t0085 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2539G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2539 | chr12 | 121778261 | |||||
| chr12:121778289
|
A | G | 3 | a0001c0001t0021a0001c0001t0060a0001c0001t0063 | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2567A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2567 | chr12 | 121778289 | |||||
| chr12:121778315
|
G | A | 1 | a0001c0001t0020 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2593G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2593 | chr12 | 121778315 | |||||
| chr12:121778324
|
G | C | 1 | a0001c0001t0030 | 2 | HG00140.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2602G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2602 | chr12 | 121778324 | |||||
| chr12:121778450
|
C | CA | 14 | a0001c0001t0007a0001c0001t0036a0001c0001t0044others(11): Show | 23 | HG00438.hp2 HG00597.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2749dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2750 | INFO_REALIGN_3_PRIME | chr12 | 121778450 | ||||
| chr12:121778450
|
C | CAA | 32 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(29): Show | 82 | HG00558.hp1 HG00597.hp2 HG01167.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2748_*2749dupAA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2750 | INFO_REALIGN_3_PRIME | chr12 | 121778450 | ||||
| chr12:121778450
|
C | CAAA | 15 | a0001c0001t0010a0001c0001t0027a0001c0001t0049others(12): Show | 20 | HG00423.hp1 HG00438.hp1 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2747_*2749dupAAA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2750 | INFO_REALIGN_3_PRIME | chr12 | 121778450 | ||||
| chr12:121778450
|
CA | C | 5 | a0001c0001t0082a0001c0004t0099a0001c0004t0100others(2): Show | 6 | HG01943.hp1 HG02809.hp2 NA18948.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2749delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2749 | INFO_REALIGN_3_PRIME | chr12 | 121778450 | ||||
| chr12:121778577
|
G | A | 1 | a0001c0001t0103 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2855G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2855 | chr12 | 121778577 | |||||
| chr12:121778624
|
G | A | 2 | a0001c0001t0013a0002c0002t0013 | 5 | NA18955.hp1 NA18956.hp1 NA18980.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2902G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2902 | chr12 | 121778624 | |||||
| chr12:121778658
|
C | T | 3 | a0001c0001t0049a0001c0001t0050a0001c0001t0051 | 3 | HG02451.hp1 HG03098.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2936C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2936 | chr12 | 121778658 | |||||
| chr12:121778716
|
A | G | 49 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(46): Show | 102 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2994A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 2994 | chr12 | 121778716 | |||||
| chr12:121778723
|
T | C | 6 | a0001c0001t0015a0001c0001t0035a0001c0001t0041others(3): Show | 11 | HG02559.hp1 HG02698.hp2 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3001T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3001 | chr12 | 121778723 | |||||
| chr12:121778986
|
A | G | 33 | a0001c0001t0003a0001c0001t0009a0001c0001t0015others(30): Show | 69 | HG00140.hp1 HG00735.hp2 HG01071.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*3264A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3264 | chr12 | 121778986 | |||||
| chr12:121779004
|
A | G | 4 | a0001c0001t0017a0002c0002t0017a0002c0002t0048others(1): Show | 6 | HG00735.hp1 HG00741.hp2 HG01109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3282A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3282 | chr12 | 121779004 | |||||
| chr12:121779015
|
C | A | 1 | a0001c0001t0109 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3293C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3293 | chr12 | 121779015 | |||||
| chr12:121779028
|
C | T | 2 | a0001c0001t0037a0002c0002t0037 | 2 | HG02683.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3306C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3306 | chr12 | 121779028 | |||||
| chr12:121779030
|
T | C | 39 | a0001c0001t0003a0001c0001t0009a0001c0001t0015others(36): Show | 76 | HG00140.hp1 HG00735.hp2 HG01071.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*3308T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3308 | chr12 | 121779030 | |||||
| chr12:121779126
|
G | A | 2 | a0001c0001t0054a0001c0001t0057 | 2 | HG02280.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3404G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3404 | chr12 | 121779126 | |||||
| chr12:121779130
|
G | A | 2 | a0001c0001t0055a0002c0002t0058 | 2 | HG02738.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3408G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3408 | chr12 | 121779130 | |||||
| chr12:121779227
|
G | A | 1 | a0002c0002t0096 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3505G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3505 | chr12 | 121779227 | |||||
| chr12:121779546
|
C | T | 1 | a0001c0001t0109 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3824C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3824 | chr12 | 121779546 | |||||
| chr12:121779611
|
C | T | 1 | a0001c0001t0090 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3889 | chr12 | 121779611 | |||||
| chr12:121779653
|
C | T | 3 | a0001c0001t0015a0001c0001t0041a0002c0002t0015 | 7 | HG02698.hp2 HG03688.hp1 HG04199.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3931C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 3931 | chr12 | 121779653 | |||||
| chr12:121779917
|
G | A | 2 | a0001c0001t0029a0001c0001t0070 | 3 | HG02055.hp1 HG02486.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4195G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4195 | chr12 | 121779917 | |||||
| chr12:121779950
|
G | GGT | 130 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(127): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*4231_*4232dupGT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4233 | INFO_REALIGN_3_PRIME | chr12 | 121779950 | ||||
| chr12:121780118
|
C | T | 1 | a0001c0001t0106 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4396C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4396 | chr12 | 121780118 | |||||
| chr12:121780160
|
C | T | 1 | a0002c0002t0089 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4438C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4438 | chr12 | 121780160 | |||||
| chr12:121780397
|
C | A | 1 | a0002c0002t0053 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4675C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4675 | chr12 | 121780397 | |||||
| chr12:121780483
|
C | T | 1 | a0001c0001t0040 | 2 | HG02258.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4761C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4761 | chr12 | 121780483 | |||||
| chr12:121780493
|
C | G | 1 | a0003c0003t0061 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4771C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4771 | chr12 | 121780493 | |||||
| chr12:121780583
|
C | G | 32 | a0001c0001t0003a0001c0001t0009a0001c0001t0015others(29): Show | 63 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4861C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 4861 | chr12 | 121780583 | |||||
| chr12:121780877
|
T | G | 6 | a0001c0001t0009a0001c0001t0046a0001c0001t0076others(3): Show | 11 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5155T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 5155 | chr12 | 121780877 | |||||
| chr12:121781094
|
C | T | 1 | a0001c0001t0090 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5372C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 5372 | chr12 | 121781094 | |||||
| chr12:121781341
|
C | T | 1 | a0001c0001t0110 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5619C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 5619 | chr12 | 121781341 | |||||
| chr12:121781485
|
C | T | 1 | a0001c0001t0028 | 2 | HG02129.hp1 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5763C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 5763 | chr12 | 121781485 | |||||
| chr12:121781544
|
G | A | 1 | a0005c0006t0047 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5822G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 5822 | chr12 | 121781544 | |||||
| chr12:121781612
|
C | G | 4 | a0001c0001t0015a0001c0001t0041a0001c0001t0109others(1): Show | 8 | HG02698.hp2 HG03688.hp1 HG04199.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5890C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 5890 | chr12 | 121781612 | |||||
| chr12:121781840
|
A | G | 2 | a0001c0001t0043a0001c0001t0044 | 2 | NA19084.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6118A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 6118 | chr12 | 121781840 | |||||
| chr12:121781881
|
T | C | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(61): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*6159T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 6159 | chr12 | 121781881 | |||||
| chr12:121781923
|
C | A | 1 | a0002c0002t0088 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6201C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 6201 | chr12 | 121781923 | |||||
| chr12:121781927
|
G | A | 2 | a0001c0001t0035a0001c0001t0078 | 3 | HG02559.hp1 HG03195.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6205G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 6205 | chr12 | 121781927 | |||||
| chr12:121782004
|
A | G | 33 | a0001c0001t0003a0001c0001t0009a0001c0001t0015others(30): Show | 69 | HG00140.hp1 HG00735.hp2 HG01071.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*6282A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 12/12 | 6282 | chr12 | 121782004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121713012
|
C | A | 1 | a0001c0001t0011g0002 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.69+48C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713012 | ||||||
| chr12:121713022
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.69+58T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713022 | ||||||
| chr12:121713280
|
G | A | 2 | a0001c0001t0009g0004a0001c0001t0009g0005 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.69+316G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713280 | ||||||
| chr12:121713470
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.69+506G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713470 | ||||||
| chr12:121713539
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+575C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713539 | ||||||
| chr12:121713616
|
C | A | 1 | a0001c0001t0101g0007 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.69+652C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713616 | ||||||
| chr12:121713659
|
C | T | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+695C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713659 | ||||||
| chr12:121713767
|
C | G | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+803C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713767 | ||||||
| chr12:121713801
|
C | T | 1 | a0001c0001t0107g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69+837C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713801 | ||||||
| chr12:121713818
|
G | A | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+854G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121713818 | ||||||
| chr12:121714089
|
G | A | 1 | a0001c0001t0005g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.69+1125G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714089 | ||||||
| chr12:121714192
|
T | C | 1 | a0002c0002t0016g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.69+1228T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714192 | ||||||
| chr12:121714295
|
C | T | 1 | a0002c0002t0015g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+1331C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714295 | ||||||
| chr12:121714318
|
G | A | 3 | a0001c0001t0021g0011a0001c0004t0003g0012a0001c0004t0099g0010 | 3 | HG02258.hp1 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.69+1354G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714318 | ||||||
| chr12:121714349
|
C | T | 4 | a0002c0002t0001g0305a0002c0002t0022g0304a0002c0002t0031g0303others(1): Show | 4 | HG01167.hp2 HG01496.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+1385C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714349 | ||||||
| chr12:121714355
|
C | G | 7 | a0001c0001t0003g0300a0001c0001t0017g0295a0001c0001t0023g0297others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+1391C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714355 | ||||||
| chr12:121714440
|
A | G | 1 | a0001c0001t0090g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.69+1476A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714440 | ||||||
| chr12:121714551
|
C | T | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+1587C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714551 | ||||||
| chr12:121714557
|
C | CT | 23 | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0004g0276others(20): Show | 23 | HG00621.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.69+1616dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121714557 | |||||
| chr12:121714895
|
C | T | 11 | a0001c0001t0001g0268a0001c0001t0004g0270a0001c0001t0006g0267others(8): Show | 11 | HG01978.hp1 HG02004.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+1931C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714895 | ||||||
| chr12:121714933
|
G | A | 67 | a0001c0001t0001g0045a0001c0001t0001g0272a0001c0001t0002g0020others(64): Show | 67 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.69+1969G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121714933 | ||||||
| chr12:121715146
|
G | A | 3 | a0001c0001t0001g0277a0001c0001t0004g0276a0002c0002t0065g0275 | 3 | HG03239.hp1 HG03239.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.69+2182G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715146 | ||||||
| chr12:121715202
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+2238G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715202 | ||||||
| chr12:121715224
|
C | A | 185 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(182): Show | 185 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.69+2260C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715224 | ||||||
| chr12:121715390
|
A | G | 1 | a0001c0001t0082g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.69+2426A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715390 | ||||||
| chr12:121715404
|
G | A | 99 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0099others(96): Show | 99 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.69+2440G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715404 | ||||||
| chr12:121715589
|
C | T | 7 | a0001c0001t0046g0067a0003c0003t0002g0069a0003c0003t0002g0274others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+2625C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715589 | ||||||
| chr12:121715590
|
G | A | 99 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0099others(96): Show | 99 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.69+2626G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715590 | ||||||
| chr12:121715724
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.69+2760C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715724 | ||||||
| chr12:121715971
|
C | T | 311 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.69+3007C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121715971 | ||||||
| chr12:121716049
|
T | TTTGGGAG others(6): Show |
4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+3096_69+3108dup others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121716049 | |||||
| chr12:121716304
|
T | C | 7 | a0001c0001t0012g0074a0001c0001t0049g0158a0001c0001t0050g0155others(4): Show | 7 | HG00642.hp1 HG01169.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+3340T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716304 | ||||||
| chr12:121716309
|
C | CA | 46 | a0001c0001t0001g0079a0001c0001t0001g0272a0001c0001t0001g0277others(43): Show | 46 | HG00621.hp1 HG01099.hp1 HG02055.hp2 others(43): Show |
intron_variant | MODIFIER | c.69+3360dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121716309 | |||||
| chr12:121716309
|
CA | C | 9 | a0001c0001t0012g0074a0001c0001t0040g0259a0001c0001t0040g0260others(6): Show | 9 | HG00642.hp1 HG01169.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+3360delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121716309 | |||||
| chr12:121716565
|
C | CT | 239 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(236): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.69+3616dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121716565 | |||||
| chr12:121716565
|
C | CTT | 35 | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0002g0147others(32): Show | 35 | HG00621.hp1 HG01433.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.69+3615_69+3616dup others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121716565 | |||||
| chr12:121716587
|
C | G | 161 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+3623C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716587 | ||||||
| chr12:121716608
|
A | G | 161 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+3644A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716608 | ||||||
| chr12:121716657
|
G | A | 161 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+3693G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716657 | ||||||
| chr12:121716711
|
C | T | 86 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0004g0203others(83): Show | 87 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+3747C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716711 | ||||||
| chr12:121716723
|
C | T | 161 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+3759C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716723 | ||||||
| chr12:121716965
|
A | G | 1 | a0002c0002t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.69+4001A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121716965 | ||||||
| chr12:121717127
|
C | T | 6 | a0001c0001t0102g0083a0002c0002t0003g0084a0002c0002t0003g0085others(3): Show | 6 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+4163C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717127 | ||||||
| chr12:121717248
|
G | A | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+4284G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717248 | ||||||
| chr12:121717278
|
G | A | 1 | a0002c0002t0003g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69+4314G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717278 | ||||||
| chr12:121717380
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.69+4416G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717380 | ||||||
| chr12:121717655
|
G | A | 6 | a0001c0001t0102g0083a0002c0002t0003g0084a0002c0002t0003g0085others(3): Show | 6 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+4691G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717655 | ||||||
| chr12:121717697
|
G | T | 5 | a0002c0002t0003g0084a0002c0002t0003g0085a0002c0002t0003g0087others(2): Show | 5 | HG02055.hp2 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+4733G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717697 | ||||||
| chr12:121717745
|
C | T | 2 | a0001c0001t0040g0259a0001c0001t0040g0260 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.69+4781C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717745 | ||||||
| chr12:121717815
|
T | G | 289 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(286): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.69+4851T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121717815 | ||||||
| chr12:121718080
|
G | C | 196 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(193): Show | 196 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.69+5116G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121718080 | ||||||
| chr12:121718228
|
A | G | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.69+5264A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121718228 | ||||||
| chr12:121718430
|
C | T | 1 | a0002c0002t0015g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+5466C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121718430 | ||||||
| chr12:121718487
|
CAG | C | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+5526_69+5527del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121718487 | |||||
| chr12:121718679
|
G | A | 1 | a0002c0002t0058g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.69+5715G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121718679 | ||||||
| chr12:121719045
|
G | A | 1 | a0002c0002t0012g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+6081G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719045 | ||||||
| chr12:121719200
|
G | C | 101 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(98): Show | 101 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.69+6236G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719200 | ||||||
| chr12:121719207
|
A | G | 2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.69+6243A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719207 | ||||||
| chr12:121719266
|
G | C | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+6302G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719266 | ||||||
| chr12:121719292
|
G | A | 165 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(162): Show | 165 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.69+6328G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719292 | ||||||
| chr12:121719342
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+6378C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719342 | ||||||
| chr12:121719648
|
C | T | 1 | a0001c0004t0003g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+6684C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719648 | ||||||
| chr12:121719787
|
C | T | 1 | a0002c0002t0007g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.69+6823C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719787 | ||||||
| chr12:121719790
|
G | T | 1 | a0002c0002t0001g0234 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.69+6826G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121719790 | ||||||
| chr12:121720112
|
T | C | 1 | a0002c0002t0001g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.69+7148T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720112 | ||||||
| chr12:121720151
|
G | A | 287 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(284): Show | 288 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.69+7187G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720151 | ||||||
| chr12:121720217
|
C | G | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+7253C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720217 | ||||||
| chr12:121720261
|
A | G | 1 | a0001c0001t0010g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.69+7297A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720261 | ||||||
| chr12:121720317
|
C | A | 3 | a0001c0001t0005g0075a0001c0001t0054g0093a0001c0001t0057g0018 | 3 | HG02280.hp1 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.69+7353C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720317 | ||||||
| chr12:121720664
|
A | G | 7 | a0001c0001t0001g0277a0001c0001t0004g0276a0002c0002t0016g0009others(4): Show | 7 | HG02451.hp2 HG02976.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+7700A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720664 | ||||||
| chr12:121720756
|
C | G | 165 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(162): Show | 165 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.69+7792C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121720756 | ||||||
| chr12:121721038
|
C | T | 1 | a0001c0001t0004g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.69+8074C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721038 | ||||||
| chr12:121721131
|
A | G | 101 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(98): Show | 101 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.69+8167A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721131 | ||||||
| chr12:121721360
|
G | A | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+8396G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721360 | ||||||
| chr12:121721378
|
C | T | 9 | a0001c0001t0003g0003a0001c0001t0003g0251a0001c0001t0003g0253others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+8414C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721378 | ||||||
| chr12:121721558
|
G | A | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.69+8594G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721558 | ||||||
| chr12:121721586
|
C | G | 1 | a0002c0002t0002g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.69+8622C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721586 | ||||||
| chr12:121721596
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.69+8632C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721596 | ||||||
| chr12:121721723
|
C | T | 1 | a0002c0002t0015g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+8759C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721723 | ||||||
| chr12:121721733
|
G | T | 29 | a0001c0001t0001g0129a0001c0001t0002g0136a0001c0001t0002g0139others(26): Show | 29 | HG00558.hp1 HG01243.hp2 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.69+8769G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721733 | ||||||
| chr12:121721804
|
C | CT | 23 | a0001c0001t0001g0179a0001c0001t0005g0008a0001c0001t0005g0059others(20): Show | 23 | HG00597.hp2 HG01928.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.69+8862dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121721804 | |||||
| chr12:121721804
|
C | CTTTTTT | 7 | a0001c0001t0002g0020a0001c0001t0005g0040a0001c0001t0037g0094others(4): Show | 7 | HG02055.hp2 HG03130.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+8857_69+8862dup others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121721804 | |||||
| chr12:121721804
|
C | CTTTTTTT | 74 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0001g0104others(71): Show | 74 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.69+8856_69+8862dup others(7): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121721804 | |||||
| chr12:121721804
|
C | CTTTTTTT others(1): Show |
23 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0118others(20): Show | 23 | HG00597.hp1 HG00621.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.69+8855_69+8862dup others(8): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121721804 | |||||
| chr12:121721804
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.69+8853_69+8862del others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121721804 | |||||
| chr12:121721814
|
T | TTTTTTC | 48 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0002g0136others(45): Show | 48 | HG00140.hp1 HG00558.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.69+8855_69+8856ins others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121721814 | |||||
| chr12:121721912
|
G | A | 1 | a0002c0002t0091g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.69+8948G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121721912 | ||||||
| chr12:121722001
|
C | G | 13 | a0001c0001t0006g0049a0001c0001t0006g0050a0001c0001t0006g0051others(10): Show | 13 | HG02040.hp2 HG02056.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.69+9037C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722001 | ||||||
| chr12:121722048
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+9084G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722048 | ||||||
| chr12:121722100
|
C | CT | 9 | a0001c0001t0006g0120a0001c0001t0011g0119a0001c0001t0015g0116others(6): Show | 9 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+9152dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121722100 | |||||
| chr12:121722100
|
CT | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0004g0203others(87): Show | 91 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.69+9152delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121722100 | |||||
| chr12:121722191
|
C | T | 1 | a0001c0001t0005g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.69+9227C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722191 | ||||||
| chr12:121722680
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0055g0095 | 2 | HG02738.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.69+9716T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722680 | ||||||
| chr12:121722696
|
T | C | 1 | a0001c0001t0111g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+9732T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722696 | ||||||
| chr12:121722848
|
C | CT | 74 | a0001c0001t0001g0006a0001c0001t0004g0203a0001c0001t0004g0217others(71): Show | 75 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.69+9901dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121722848 | |||||
| chr12:121722848
|
CT | C | 164 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(161): Show | 164 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.69+9901delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121722848 | |||||
| chr12:121722908
|
G | A | 1 | a0002c0002t0004g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.69+9944G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722908 | ||||||
| chr12:121722911
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+9947C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121722911 | ||||||
| chr12:121723036
|
C | T | 2 | a0001c0001t0005g0113a0001c0001t0083g0114 | 2 | HG00544.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.69+10072C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723036 | ||||||
| chr12:121723037
|
G | A | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+10073G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723037 | ||||||
| chr12:121723146
|
T | TTTTG | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0035others(1): Show | 4 | HG03017.hp1 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+10202_69+10205d others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121723146 | |||||
| chr12:121723146
|
TTTTG | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0004g0203others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.69+10202_69+10205d others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121723146 | |||||
| chr12:121723461
|
A | C | 1 | a0002c0002t0001g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.69+10497A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723461 | ||||||
| chr12:121723462
|
C | T | 1 | a0002c0002t0001g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.69+10498C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723462 | ||||||
| chr12:121723478
|
G | A | 1 | a0002c0002t0008g0309 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.69+10514G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723478 | ||||||
| chr12:121723587
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.69+10623C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723587 | ||||||
| chr12:121723845
|
C | T | 166 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(163): Show | 166 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.69+10881C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723845 | ||||||
| chr12:121723923
|
C | T | 1 | a0001c0001t0079g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69+10959C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723923 | ||||||
| chr12:121723924
|
G | A | 1 | a0001c0001t0036g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.69+10960G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121723924 | ||||||
| chr12:121724030
|
C | CT | 103 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0002g0139others(100): Show | 104 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.69+11091dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121724030 | |||||
| chr12:121724030
|
C | CTT | 12 | a0001c0001t0005g0008a0001c0001t0009g0152a0001c0001t0012g0074others(9): Show | 12 | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+11090_69+11091d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121724030 | |||||
| chr12:121724030
|
CTTTTTTT | C | 95 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0099others(92): Show | 95 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.69+11085_69+11091d others(9): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121724030 | |||||
| chr12:121724238
|
T | C | 4 | a0001c0001t0021g0011a0001c0004t0003g0012a0001c0004t0099g0010others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+11274T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121724238 | ||||||
| chr12:121724260
|
C | A | 4 | a0001c0001t0001g0277a0001c0001t0004g0276a0002c0002t0016g0286others(1): Show | 4 | HG03239.hp1 HG03239.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+11296C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121724260 | ||||||
| chr12:121724559
|
G | A | 17 | a0001c0001t0003g0148a0001c0001t0005g0008a0001c0001t0005g0059others(14): Show | 17 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.69+11595G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121724559 | ||||||
| chr12:121724615
|
GT | G | 277 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(274): Show | 278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.69+11664delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121724615 | |||||
| chr12:121724759
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.69+11795C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121724759 | ||||||
| chr12:121724941
|
T | C | 281 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(278): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.69+11977T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121724941 | ||||||
| chr12:121725042
|
A | G | 6 | a0001c0001t0102g0083a0002c0002t0003g0084a0002c0002t0003g0085others(3): Show | 6 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+12078A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121725042 | ||||||
| chr12:121725370
|
G | A | 168 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(165): Show | 168 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.69+12406G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121725370 | ||||||
| chr12:121725372
|
G | C | 1 | a0002c0002t0010g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69+12408G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121725372 | ||||||
| chr12:121725529
|
C | T | 1 | a0001c0001t0087g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.69+12565C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121725529 | ||||||
| chr12:121725573
|
TCAAAACA others(3): Show |
T | 1 | a0002c0002t0086g0291 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.69+12614_69+12623d others(12): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121725573 | |||||
| chr12:121725863
|
C | T | 1 | a0002c0002t0004g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.69+12899C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121725863 | ||||||
| chr12:121725882
|
C | A | 1 | a0002c0002t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.69+12918C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121725882 | ||||||
| chr12:121726035
|
C | CA | 153 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0104others(150): Show | 153 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.69+13084dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726035 | |||||
| chr12:121726035
|
C | CAA | 112 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0099others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.69+13083_69+13084d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726035 | |||||
| chr12:121726035
|
C | CAAA | 7 | a0001c0001t0006g0056a0001c0001t0006g0117a0001c0001t0028g0240others(4): Show | 7 | HG01496.hp2 HG02083.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+13082_69+13084d others(5): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726035 | |||||
| chr12:121726049
|
C | A | 8 | a0001c0001t0001g0268a0001c0001t0001g0313a0001c0001t0004g0041others(5): Show | 8 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+13085C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726049 | ||||||
| chr12:121726049
|
C | CA | 8 | a0001c0001t0003g0300a0001c0001t0017g0295a0001c0001t0023g0297others(5): Show | 8 | HG00323.hp2 HG00738.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+13095dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726049 | |||||
| chr12:121726054
|
A | G | 1 | a0001c0004t0003g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+13090A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726054 | ||||||
| chr12:121726144
|
G | C | 1 | a0001c0001t0009g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.69+13180G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726144 | ||||||
| chr12:121726175
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+13211G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726175 | ||||||
| chr12:121726297
|
C | T | 4 | a0001c0001t0021g0011a0001c0004t0003g0012a0001c0004t0099g0010others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+13333C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726297 | ||||||
| chr12:121726472
|
G | A | 5 | a0001c0001t0001g0129a0001c0001t0066g0138a0002c0002t0004g0128others(2): Show | 5 | HG02071.hp1 HG02155.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+13508G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726472 | ||||||
| chr12:121726518
|
G | A | 3 | a0002c0002t0031g0091a0002c0002t0031g0303a0002c0002t0039g0302 | 3 | HG01496.hp2 HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.69+13554G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726518 | ||||||
| chr12:121726578
|
C | CA | 189 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(186): Show | 189 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.69+13625dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726578 | |||||
| chr12:121726590
|
T | A | 173 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(170): Show | 173 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.69+13626T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726590 | ||||||
| chr12:121726592
|
A | T | 1 | a0001c0004t0003g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+13628A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726592 | ||||||
| chr12:121726595
|
T | A | 3 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311 | 3 | NA19054.hp1 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.69+13631T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726595 | ||||||
| chr12:121726597
|
A | AT | 6 | a0001c0001t0021g0011a0001c0001t0044g0312a0001c0004t0003g0012others(3): Show | 6 | HG02258.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+13633_69+13634i others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726597 | ||||||
| chr12:121726822
|
T | A | 1 | a0001c0001t0072g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.69+13858T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121726822 | ||||||
| chr12:121726907
|
C | CA | 22 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0185others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.69+13972dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
C | CAAAAA | 8 | a0001c0001t0003g0148a0001c0001t0004g0276a0001c0001t0009g0004others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+13968_69+13972d others(7): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
C | CAAAAAA | 8 | a0001c0001t0001g0277a0001c0001t0005g0008a0001c0001t0005g0059others(5): Show | 8 | HG02486.hp2 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+13967_69+13972d others(8): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0016g0061a0001c0001t0044g0312a0001c0001t0063g0062others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+13965_69+13972d others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
CA | C | 7 | a0002c0002t0001g0222a0002c0002t0008g0221a0002c0002t0008g0223others(4): Show | 7 | HG01496.hp1 HG02155.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+13972delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0001g0268a0001c0001t0004g0041a0001c0001t0015g0269others(3): Show | 6 | HG00280.hp2 HG03195.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+13963_69+13972d others(12): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
CAAAAAAA others(4): Show |
C | 117 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(114): Show | 117 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.69+13962_69+13972d others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
CAAAAAAA others(5): Show |
C | 49 | a0001c0001t0001g0129a0001c0001t0002g0030a0001c0001t0002g0057others(46): Show | 49 | HG00140.hp1 HG00558.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.69+13961_69+13972d others(14): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121726907
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0020g0126 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.69+13960_69+13972d others(15): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121726907 | |||||
| chr12:121727080
|
A | G | 1 | a0001c0001t0074g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.69+14116A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121727080 | ||||||
| chr12:121727440
|
G | A | 1 | a0002c0002t0065g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.69+14476G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121727440 | ||||||
| chr12:121727536
|
C | CA | 28 | a0001c0001t0001g0176a0001c0001t0003g0148a0001c0001t0003g0300others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.69+14595dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121727536 | |||||
| chr12:121727548
|
A | AG | 170 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(167): Show | 170 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.69+14584_69+14585i others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121727548 | ||||||
| chr12:121727548
|
A | G | 1 | a0001c0001t0020g0126 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.69+14584A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121727548 | ||||||
| chr12:121727746
|
C | T | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+14782C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121727746 | ||||||
| chr12:121727873
|
C | CAA | 73 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0004g0203others(70): Show | 74 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.69+14927_69+14928d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121727873 | |||||
| chr12:121727873
|
CA | C | 23 | a0001c0001t0001g0277a0001c0001t0002g0057a0001c0001t0003g0148others(20): Show | 23 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.69+14928delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121727873 | |||||
| chr12:121728047
|
G | A | 2 | a0001c0001t0016g0308a0001c0009t0018g0131 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.69+15083G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728047 | ||||||
| chr12:121728206
|
C | T | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+15242C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728206 | ||||||
| chr12:121728228
|
G | A | 1 | a0001c0001t0016g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.69+15264G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728228 | ||||||
| chr12:121728362
|
G | A | 8 | a0002c0002t0001g0184a0002c0002t0001g0201a0002c0002t0004g0224others(5): Show | 8 | HG02071.hp2 HG02132.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-15267G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728362 | ||||||
| chr12:121728399
|
G | A | 1 | a0001c0001t0051g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.70-15230G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728399 | ||||||
| chr12:121728412
|
T | C | 24 | a0001c0001t0001g0277a0001c0001t0003g0148a0001c0001t0004g0276others(21): Show | 24 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-15217T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728412 | ||||||
| chr12:121728488
|
CA | C | 6 | a0001c0001t0008g0115a0001c0001t0026g0015a0001c0001t0026g0016others(3): Show | 6 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-15126delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121728488 | |||||
| chr12:121728502
|
A | G | 1 | a0001c0001t0074g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70-15127A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728502 | ||||||
| chr12:121728540
|
A | G | 201 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(198): Show | 201 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.70-15089A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728540 | ||||||
| chr12:121728571
|
C | T | 57 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0002g0136others(54): Show | 57 | HG00140.hp1 HG00558.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.70-15058C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728571 | ||||||
| chr12:121728784
|
A | G | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.70-14845A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121728784 | ||||||
| chr12:121729000
|
C | T | 3 | a0001c0001t0002g0147a0001c0001t0033g0145a0001c0001t0084g0146 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.70-14629C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729000 | ||||||
| chr12:121729159
|
G | A | 1 | a0001c0001t0011g0002 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.70-14470G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729159 | ||||||
| chr12:121729161
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.70-14468T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729161 | ||||||
| chr12:121729189
|
C | T | 106 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(103): Show | 106 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.70-14440C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729189 | ||||||
| chr12:121729207
|
C | T | 3 | a0001c0001t0006g0055a0001c0001t0006g0120a0001c0001t0052g0054 | 3 | HG02080.hp1 NA18964.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.70-14422C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729207 | ||||||
| chr12:121729452
|
A | C | 1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70-14177A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729452 | ||||||
| chr12:121729639
|
GA | G | 19 | a0001c0001t0003g0148a0001c0001t0005g0008a0001c0001t0005g0059others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-13976delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121729639 | |||||
| chr12:121729665
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-13964G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729665 | ||||||
| chr12:121729787
|
C | T | 58 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0002g0136others(55): Show | 58 | HG00140.hp1 HG00558.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.70-13842C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729787 | ||||||
| chr12:121729912
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.70-13717G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729912 | ||||||
| chr12:121729913
|
C | T | 1 | a0001c0001t0111g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-13716C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729913 | ||||||
| chr12:121729914
|
G | A | 4 | a0001c0001t0021g0011a0001c0004t0003g0012a0001c0004t0099g0010others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-13715G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729914 | ||||||
| chr12:121729989
|
G | A | 167 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.70-13640G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121729989 | ||||||
| chr12:121730218
|
C | T | 2 | a0001c0001t0009g0151a0001c0001t0016g0308 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.70-13411C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730218 | ||||||
| chr12:121730257
|
C | CA | 8 | a0001c0001t0001g0277a0001c0001t0004g0276a0001c0001t0005g0042others(5): Show | 8 | HG02976.hp2 HG03239.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-13357dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730257 | |||||
| chr12:121730257
|
CA | C | 7 | a0001c0001t0006g0033a0001c0001t0008g0115a0001c0001t0020g0125others(4): Show | 7 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-13357delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730257 | |||||
| chr12:121730273
|
G | A | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70-13356G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730273 | ||||||
| chr12:121730308
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.70-13321G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730308 | ||||||
| chr12:121730482
|
TA | T | 280 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(277): Show | 281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.70-13136delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730482 | |||||
| chr12:121730600
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-13029G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730600 | ||||||
| chr12:121730628
|
C | T | 2 | a0001c0001t0032g0141a0001c0001t0032g0142 | 2 | HG00558.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.70-13001C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730628 | ||||||
| chr12:121730647
|
C | CA | 87 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.70-12966dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730647 | |||||
| chr12:121730647
|
C | CAA | 28 | a0001c0001t0001g0272a0001c0001t0002g0020a0001c0001t0002g0021others(25): Show | 28 | HG00544.hp1 HG00621.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.70-12967_70-12966d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730647 | |||||
| chr12:121730647
|
CA | C | 72 | a0001c0001t0001g0006a0001c0001t0004g0217a0001c0001t0004g0233others(69): Show | 73 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.70-12966delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730647 | |||||
| chr12:121730660
|
A | C | 1 | a0001c0001t0066g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.70-12969A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730660 | ||||||
| chr12:121730664
|
C | A | 1 | a0003c0003t0002g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70-12965C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730664 | ||||||
| chr12:121730668
|
C | A | 2 | a0002c0002t0004g0204a0002c0002t0085g0205 | 2 | HG03491.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.70-12961C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730668 | ||||||
| chr12:121730668
|
C | CA | 7 | a0001c0001t0005g0060a0001c0001t0006g0117a0001c0001t0023g0301others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-12952dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121730668 | |||||
| chr12:121730683
|
C | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0004g0203others(77): Show | 81 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.70-12946C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730683 | ||||||
| chr12:121730728
|
C | T | 1 | a0001c0001t0007g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.70-12901C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730728 | ||||||
| chr12:121730861
|
G | A | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.70-12768G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121730861 | ||||||
| chr12:121731027
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0004g0276a0002c0002t0016g0009others(2): Show | 5 | HG02451.hp2 HG03239.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-12602C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121731027 | ||||||
| chr12:121731337
|
T | C | 1 | a0001c0001t0042g0250 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.70-12292T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121731337 | ||||||
| chr12:121731554
|
G | A | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-12075G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121731554 | ||||||
| chr12:121731749
|
G | A | 5 | a0001c0001t0002g0022a0001c0001t0002g0028a0001c0001t0002g0030others(2): Show | 5 | NA18940.hp1 NA18956.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-11880G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121731749 | ||||||
| chr12:121731978
|
C | A | 214 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.70-11651C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121731978 | ||||||
| chr12:121732079
|
G | A | 1 | a0002c0002t0091g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70-11550G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732079 | ||||||
| chr12:121732095
|
C | T | 3 | a0001c0001t0035g0133a0001c0001t0035g0134a0001c0001t0078g0132 | 3 | HG02559.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70-11534C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732095 | ||||||
| chr12:121732250
|
C | T | 1 | a0001c0007t0026g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70-11379C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732250 | ||||||
| chr12:121732399
|
G | T | 36 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0003g0148others(33): Show | 36 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.70-11230G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732399 | ||||||
| chr12:121732629
|
G | A | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-11000G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732629 | ||||||
| chr12:121732702
|
G | A | 1 | a0001c0001t0008g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70-10927G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732702 | ||||||
| chr12:121732825
|
A | G | 1 | a0001c0001t0111g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-10804A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732825 | ||||||
| chr12:121732889
|
G | C | 3 | a0001c0001t0015g0096a0001c0001t0015g0101a0001c0001t0015g0116 | 3 | HG02698.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.70-10740G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732889 | ||||||
| chr12:121732933
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-10696C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121732933 | ||||||
| chr12:121732978
|
C | CA | 12 | a0001c0001t0005g0042a0001c0001t0021g0013a0001c0001t0030g0159others(9): Show | 12 | HG01106.hp1 HG01106.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-10633dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121732978 | |||||
| chr12:121732978
|
CA | C | 6 | a0001c0001t0001g0118a0001c0001t0005g0040a0001c0001t0005g0113others(3): Show | 6 | HG00423.hp1 HG00544.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-10633delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121732978 | |||||
| chr12:121733094
|
C | T | 25 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0268others(22): Show | 25 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.70-10535C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733094 | ||||||
| chr12:121733108
|
A | G | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.70-10521A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733108 | ||||||
| chr12:121733128
|
A | G | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-10501A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733128 | ||||||
| chr12:121733330
|
C | T | 12 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(9): Show | 12 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-10299C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733330 | ||||||
| chr12:121733534
|
G | A | 1 | a0001c0001t0005g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70-10095G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733534 | ||||||
| chr12:121733548
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.70-10081T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733548 | ||||||
| chr12:121733678
|
C | T | 1 | a0001c0001t0008g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.70-9951C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733678 | ||||||
| chr12:121733790
|
G | A | 3 | a0001c0001t0035g0133a0001c0001t0035g0134a0001c0001t0078g0132 | 3 | HG02559.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70-9839G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121733790 | ||||||
| chr12:121734100
|
C | T | 21 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0006g0049others(18): Show | 21 | HG00423.hp2 HG02040.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.70-9529C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734100 | ||||||
| chr12:121734165
|
CTG | C | 166 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(163): Show | 166 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.70-9461_70-9460del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121734165 | |||||
| chr12:121734249
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-9380G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734249 | ||||||
| chr12:121734266
|
C | CT | 20 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0006g0049others(17): Show | 20 | HG00423.hp2 HG02040.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-9354dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121734266 | |||||
| chr12:121734320
|
A | G | 216 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.70-9309A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734320 | ||||||
| chr12:121734478
|
G | A | 45 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0277others(42): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.70-9151G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734478 | ||||||
| chr12:121734518
|
A | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0003g0300others(78): Show | 82 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.70-9111A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734518 | ||||||
| chr12:121734582
|
T | G | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70-9047T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734582 | ||||||
| chr12:121734756
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0005g0040a0001c0001t0056g0047 | 3 | HG00423.hp1 NA19003.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.70-8873T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734756 | ||||||
| chr12:121734784
|
G | T | 3 | a0001c0001t0002g0147a0001c0001t0033g0145a0001c0001t0084g0146 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.70-8845G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734784 | ||||||
| chr12:121734894
|
CAA | C | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0092g0124 | 3 | HG00140.hp1 HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.70-8734_70-8733del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121734894 | ||||||
| chr12:121735059
|
G | A | 1 | a0002c0002t0014g0127 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.70-8570G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735059 | ||||||
| chr12:121735089
|
G | A | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-8540G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735089 | ||||||
| chr12:121735185
|
C | CA | 70 | a0001c0001t0001g0129a0001c0001t0002g0026a0001c0001t0002g0057others(67): Show | 70 | HG00140.hp1 HG00558.hp1 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.70-8429dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121735185 | |||||
| chr12:121735185
|
C | CAA | 6 | a0001c0001t0002g0147a0001c0001t0033g0145a0001c0001t0076g0287others(3): Show | 6 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-8430_70-8429dup others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121735185 | |||||
| chr12:121735201
|
C | A | 3 | a0001c0001t0040g0259a0001c0001t0040g0260a0003c0003t0002g0069 | 3 | HG02258.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.70-8428C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735201 | ||||||
| chr12:121735202
|
A | C | 2 | a0001c0001t0040g0259a0001c0001t0040g0260 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.70-8427A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735202 | ||||||
| chr12:121735211
|
A | C | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-8418A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735211 | ||||||
| chr12:121735403
|
AT | A | 48 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0277others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.70-8212delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121735403 | |||||
| chr12:121735618
|
C | T | 1 | a0001c0001t0071g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.70-8011C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735618 | ||||||
| chr12:121735653
|
T | C | 3 | a0001c0004t0003g0012a0001c0004t0099g0010a0001c0004t0100g0082 | 3 | HG02809.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.70-7976T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735653 | ||||||
| chr12:121735663
|
C | G | 1 | a0002c0002t0045g0043 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.70-7966C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735663 | ||||||
| chr12:121735696
|
C | CT | 8 | a0001c0001t0070g0063a0002c0002t0003g0084a0002c0002t0003g0085others(5): Show | 8 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-7921dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121735696 | |||||
| chr12:121735699
|
T | G | 1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70-7930T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735699 | ||||||
| chr12:121735776
|
C | T | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-7853C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121735776 | ||||||
| chr12:121736038
|
A | G | 1 | a0002c0002t0022g0219 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.70-7591A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736038 | ||||||
| chr12:121736077
|
G | A | 4 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311others(1): Show | 4 | NA19005.hp2 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-7552G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736077 | ||||||
| chr12:121736165
|
T | TTTTA | 85 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0003g0300others(82): Show | 86 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.70-7444_70-7441dup others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736165 | |||||
| chr12:121736205
|
C | T | 1 | a0001c0001t0006g0172 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.70-7424C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736205 | ||||||
| chr12:121736227
|
T | G | 1 | a0002c0002t0022g0304 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.70-7402T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736227 | ||||||
| chr12:121736327
|
G | GT | 36 | a0001c0001t0001g0185a0001c0001t0001g0272a0001c0001t0004g0217others(33): Show | 36 | HG00621.hp1 HG00673.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.70-7288dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736327 | |||||
| chr12:121736327
|
G | GTT | 15 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(12): Show | 15 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-7289_70-7288dup others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736327 | |||||
| chr12:121736327
|
GT | G | 11 | a0001c0001t0003g0003a0001c0001t0003g0247a0001c0001t0003g0248others(8): Show | 11 | HG00140.hp1 HG01975.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.70-7288delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736327 | |||||
| chr12:121736403
|
T | TGTGATCC others(165): Show |
1 | a0002c0002t0010g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.70-7130_70-7129ins others(172): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736403 | |||||
| chr12:121736414
|
CGCCTTGG others(79): Show |
C | 1 | a0001c0001t0009g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-7182_70-7097del others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736414 | |||||
| chr12:121736463
|
C | T | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70-7166C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736463 | ||||||
| chr12:121736533
|
T | C | 3 | a0001c0001t0002g0147a0001c0001t0033g0145a0001c0001t0084g0146 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.70-7096T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736533 | ||||||
| chr12:121736550
|
G | A | 298 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(295): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.70-7079G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736550 | ||||||
| chr12:121736602
|
C | T | 8 | a0003c0003t0002g0069a0003c0003t0002g0274a0003c0003t0002g0284others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-7027C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736602 | ||||||
| chr12:121736642
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.70-6987C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736642 | ||||||
| chr12:121736681
|
C | T | 8 | a0001c0001t0001g0277a0001c0001t0004g0041a0001c0001t0004g0276others(5): Show | 8 | HG00280.hp2 HG02451.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-6948C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736681 | ||||||
| chr12:121736693
|
GCATGCAC others(3): Show |
G | 1 | a0002c0002t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.70-6933_70-6924del others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121736693 | |||||
| chr12:121736795
|
T | A | 1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.70-6834T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121736795 | ||||||
| chr12:121737006
|
A | T | 1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.70-6623A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121737006 | ||||||
| chr12:121737271
|
G | A | 1 | a0001c0001t0090g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.70-6358G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121737271 | ||||||
| chr12:121737280
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.70-6349G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121737280 | ||||||
| chr12:121737286
|
C | T | 1 | a0001c0001t0044g0312 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.70-6343C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121737286 | ||||||
| chr12:121737568
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.70-6061T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121737568 | ||||||
| chr12:121738012
|
C | CA | 41 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0179others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.70-5600dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121738012 | |||||
| chr12:121738014
|
A | C | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.70-5615A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121738014 | ||||||
| chr12:121738127
|
C | T | 1 | a0001c0001t0097g0311 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.70-5502C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121738127 | ||||||
| chr12:121738207
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.70-5422C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121738207 | ||||||
| chr12:121738504
|
A | G | 1 | a0002c0002t0058g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.70-5125A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121738504 | ||||||
| chr12:121738860
|
C | T | 1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.70-4769C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121738860 | ||||||
| chr12:121738983
|
TC | T | 53 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0002g0136others(50): Show | 53 | HG00140.hp1 HG00558.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.70-4644delC | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121738983 | |||||
| chr12:121739016
|
G | A | 1 | a0002c0002t0007g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.70-4613G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739016 | ||||||
| chr12:121739074
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-4555C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739074 | ||||||
| chr12:121739111
|
C | T | 1 | a0002c0002t0038g0216 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.70-4518C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739111 | ||||||
| chr12:121739179
|
C | T | 1 | a0001c0001t0003g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70-4450C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739179 | ||||||
| chr12:121739211
|
C | T | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.70-4418C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739211 | ||||||
| chr12:121739228
|
C | T | 2 | a0002c0002t0009g0058a0002c0002t0053g0064 | 2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.70-4401C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739228 | ||||||
| chr12:121739416
|
A | G | 205 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.70-4213A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739416 | ||||||
| chr12:121739476
|
ACTT | A | 47 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0002g0136others(44): Show | 47 | HG00140.hp1 HG00558.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.70-4149_70-4147del others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121739476 | |||||
| chr12:121739705
|
C | T | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-3924C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739705 | ||||||
| chr12:121739798
|
C | CT | 12 | a0001c0001t0001g0006a0001c0001t0020g0125a0001c0001t0020g0126others(9): Show | 12 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-3808dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121739798 | |||||
| chr12:121739798
|
CT | C | 150 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.70-3808delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121739798 | |||||
| chr12:121739867
|
C | T | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70-3762C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739867 | ||||||
| chr12:121739871
|
C | T | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70-3758C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121739871 | ||||||
| chr12:121740205
|
C | A | 1 | a0001c0001t0004g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70-3424C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740205 | ||||||
| chr12:121740239
|
C | G | 46 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0002g0136others(43): Show | 46 | HG00140.hp1 HG00558.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.70-3390C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740239 | ||||||
| chr12:121740344
|
C | T | 40 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0179others(37): Show | 40 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.70-3285C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740344 | ||||||
| chr12:121740357
|
G | T | 6 | a0001c0001t0016g0308a0002c0002t0009g0058a0002c0002t0016g0009others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-3272G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740357 | ||||||
| chr12:121740425
|
C | T | 3 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0075 | 3 | HG02723.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.70-3204C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740425 | ||||||
| chr12:121740537
|
T | A | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-3092T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740537 | ||||||
| chr12:121740663
|
C | T | 1 | a0001c0001t0107g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.70-2966C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740663 | ||||||
| chr12:121740718
|
C | T | 1 | a0002c0002t0104g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-2911C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740718 | ||||||
| chr12:121740977
|
G | A | 1 | a0001c0001t0092g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-2652G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121740977 | ||||||
| chr12:121741034
|
T | G | 1 | a0003c0003t0009g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70-2595T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741034 | ||||||
| chr12:121741142
|
C | T | 1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.70-2487C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741142 | ||||||
| chr12:121741159
|
G | A | 1 | a0002c0002t0007g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70-2470G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741159 | ||||||
| chr12:121741393
|
G | T | 1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.70-2236G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741393 | ||||||
| chr12:121741458
|
T | C | 1 | a0001c0001t0005g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70-2171T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741458 | ||||||
| chr12:121741534
|
A | G | 304 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(301): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.70-2095A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741534 | ||||||
| chr12:121741620
|
C | T | 2 | a0001c0001t0029g0076a0001c0001t0029g0077 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70-2009C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741620 | ||||||
| chr12:121741751
|
G | C | 1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.70-1878G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741751 | ||||||
| chr12:121741926
|
C | G | 1 | a0001c0001t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70-1703C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121741926 | ||||||
| chr12:121742299
|
G | A | 6 | a0002c0002t0003g0084a0002c0002t0003g0085a0002c0002t0003g0087others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-1330G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742299 | ||||||
| chr12:121742300
|
GC | G | 3 | a0002c0002t0017g0088a0002c0002t0017g0279a0002c0002t0048g0089 | 3 | HG00735.hp1 HG00741.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.70-1327delC | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121742300 | |||||
| chr12:121742409
|
T | C | 6 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-1220T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742409 | ||||||
| chr12:121742446
|
C | A | 1 | a0002c0002t0003g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70-1183C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742446 | ||||||
| chr12:121742481
|
G | A | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.70-1148G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742481 | ||||||
| chr12:121742699
|
CCTCAGT | C | 69 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0176others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.70-926_70-921delAG others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121742699 | |||||
| chr12:121742735
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0022g0098a0001c0001t0037g0094 | 3 | HG03710.hp2 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.70-894G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742735 | ||||||
| chr12:121742808
|
C | T | 1 | a0001c0001t0023g0298 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.70-821C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742808 | ||||||
| chr12:121742978
|
T | A | 1 | a0001c0001t0002g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.70-651T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121742978 | ||||||
| chr12:121743038
|
G | A | 56 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0104others(53): Show | 56 | HG00423.hp1 HG00544.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.70-591G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121743038 | ||||||
| chr12:121743217
|
T | C | 203 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(200): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.70-412T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121743217 | ||||||
| chr12:121743278
|
T | C | 214 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.70-351T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121743278 | ||||||
| chr12:121743284
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0013g0168 | 2 | NA18980.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.70-345G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121743284 | ||||||
| chr12:121743346
|
CGAGACCA others(4): Show |
C | 1 | a0001c0001t0033g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70-281_70-271delAG others(9): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121743346 | |||||
| chr12:121743395
|
C | CA | 27 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(24): Show | 27 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.70-221dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 121743395 | |||||
| chr12:121743481
|
C | G | 1 | a0002c0002t0004g0090 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.70-148C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121743481 | ||||||
| chr12:121743508
|
A | G | 29 | a0001c0001t0001g0272a0001c0001t0002g0020a0001c0001t0002g0021others(26): Show | 29 | HG00621.hp1 HG02040.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.70-121A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 1/11 | chr12 | 121743508 | ||||||
| chr12:121743770
|
G | C | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.188+23G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121743770 | ||||||
| chr12:121744052
|
C | CT | 6 | a0001c0001t0001g0045a0001c0001t0005g0008a0001c0001t0041g0262others(3): Show | 6 | HG02738.hp2 HG04184.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.188+324dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121744052 | |||||
| chr12:121744052
|
CT | C | 8 | a0001c0001t0004g0276a0001c0001t0007g0266a0001c0001t0020g0125others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+324delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121744052 | |||||
| chr12:121744054
|
T | C | 3 | a0001c0001t0001g0176a0001c0001t0029g0076a0001c0001t0029g0077 | 3 | HG02486.hp1 HG03195.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.188+307T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121744054 | ||||||
| chr12:121744085
|
C | A | 3 | a0001c0001t0035g0133a0001c0001t0035g0134a0001c0001t0078g0132 | 3 | HG02559.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.188+338C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121744085 | ||||||
| chr12:121744458
|
C | T | 5 | a0001c0001t0011g0002a0001c0001t0011g0102a0001c0001t0011g0110others(2): Show | 5 | HG01433.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+711C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121744458 | ||||||
| chr12:121744586
|
C | T | 3 | a0002c0002t0001g0201a0002c0002t0007g0202a0002c0002t0007g0220 | 3 | HG02071.hp2 NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.188+839C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121744586 | ||||||
| chr12:121744949
|
C | T | 24 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(21): Show | 24 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.188+1202C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121744949 | ||||||
| chr12:121745057
|
G | A | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188+1310G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745057 | ||||||
| chr12:121745115
|
G | A | 1 | a0001c0001t0076g0287 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.188+1368G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745115 | ||||||
| chr12:121745215
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188+1468C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745215 | ||||||
| chr12:121745236
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.188+1489C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745236 | ||||||
| chr12:121745464
|
C | T | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+1717C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745464 | ||||||
| chr12:121745625
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.188+1878T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745625 | ||||||
| chr12:121745753
|
C | T | 9 | a0001c0001t0002g0057a0003c0003t0002g0069a0003c0003t0002g0274others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+2006C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745753 | ||||||
| chr12:121745892
|
T | C | 30 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.188+2145T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745892 | ||||||
| chr12:121745916
|
C | T | 7 | a0002c0002t0004g0128a0002c0002t0014g0127a0002c0002t0014g0196others(4): Show | 7 | HG01071.hp2 HG01255.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+2169C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121745916 | ||||||
| chr12:121746181
|
G | GC | 44 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0185others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.189-2138dupC | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121746181 | |||||
| chr12:121746188
|
CA | C | 12 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0009g0151others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-2137delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746188 | ||||||
| chr12:121746189
|
A | C | 13 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.189-2137A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746189 | ||||||
| chr12:121746190
|
C | CT | 7 | a0001c0001t0054g0093a0001c0001t0057g0018a0001c0001t0069g0019others(4): Show | 7 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-2122dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121746190 | |||||
| chr12:121746191
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-2135T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746191 | ||||||
| chr12:121746218
|
G | C | 1 | a0002c0002t0004g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189-2108G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746218 | ||||||
| chr12:121746251
|
G | A | 1 | a0001c0001t0097g0311 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.189-2075G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746251 | ||||||
| chr12:121746290
|
C | A | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-2036C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746290 | ||||||
| chr12:121746291
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.189-2035G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746291 | ||||||
| chr12:121746296
|
T | G | 1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-2030T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746296 | ||||||
| chr12:121746312
|
C | T | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-2014C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746312 | ||||||
| chr12:121746532
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-1794T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746532 | ||||||
| chr12:121746541
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189-1785C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746541 | ||||||
| chr12:121746677
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0022g0098others(1): Show | 4 | HG03710.hp2 HG03831.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1649G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746677 | ||||||
| chr12:121746680
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-1646C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746680 | ||||||
| chr12:121746750
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-1576C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746750 | ||||||
| chr12:121746778
|
C | A | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-1548C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746778 | ||||||
| chr12:121746798
|
C | A | 1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189-1528C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746798 | ||||||
| chr12:121746803
|
A | G | 1 | a0002c0002t0004g0090 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-1523A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746803 | ||||||
| chr12:121746814
|
T | C | 1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-1512T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746814 | ||||||
| chr12:121746818
|
C | T | 104 | a0002c0002t0001g0170a0002c0002t0001g0177a0002c0002t0001g0184others(101): Show | 105 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.189-1508C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746818 | ||||||
| chr12:121746824
|
G | A | 1 | a0001c0001t0079g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.189-1502G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746824 | ||||||
| chr12:121746826
|
C | T | 1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-1500C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746826 | ||||||
| chr12:121746827
|
A | G | 1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-1499A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746827 | ||||||
| chr12:121746890
|
G | A | 18 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.189-1436G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121746890 | ||||||
| chr12:121746957
|
CA | C | 32 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.189-1358delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121746957 | |||||
| chr12:121747017
|
C | A | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189-1309C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747017 | ||||||
| chr12:121747093
|
G | T | 1 | a0002c0002t0002g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.189-1233G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747093 | ||||||
| chr12:121747121
|
G | A | 2 | a0001c0001t0042g0250a0001c0001t0042g0252 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.189-1205G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747121 | ||||||
| chr12:121747237
|
G | C | 1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-1089G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747237 | ||||||
| chr12:121747249
|
A | ACTGGGGT others(73): Show |
1 | a0002c0002t0004g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.189-1065_189-1064i others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(13): Show |
4 | a0001c0001t0002g0136a0001c0001t0033g0135a0001c0001t0042g0252others(1): Show | 4 | HG00544.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1063_189-1044d others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(1113): Show |
2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-1056_189-1055i others(1122): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(53): Show |
6 | a0002c0002t0012g0163a0002c0002t0012g0174a0002c0002t0012g0175others(3): Show | 6 | HG02622.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-1044_189-1043i others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(73): Show |
76 | a0002c0002t0001g0170a0002c0002t0001g0184a0002c0002t0001g0189others(73): Show | 77 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.189-1044_189-1043i others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(73): Show |
1 | a0002c0002t0031g0091 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(93): Show |
9 | a0001c0001t0002g0020a0001c0001t0002g0028a0001c0001t0006g0055others(6): Show | 9 | HG02080.hp1 HG02451.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.189-1044_189-1043i others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(133): Show |
1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(142): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(801): Show |
2 | a0001c0001t0054g0093a0001c0001t0057g0018 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.189-1044_189-1043i others(810): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(133): Show |
1 | a0002c0002t0053g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(142): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747249
|
A | ACTGGGGT others(133): Show |
1 | a0002c0002t0007g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(142): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747249 | |||||
| chr12:121747258
|
G | GAAGGTGG others(53): Show |
1 | a0002c0002t0004g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747258 | |||||
| chr12:121747258
|
G | GAAGGTGG others(399): Show |
1 | a0002c0002t0008g0292 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(408): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747258 | |||||
| chr12:121747263
|
T | C | 1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-1063T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747263 | ||||||
| chr12:121747263
|
T | TGGGAGGC others(877): Show |
1 | a0001c0001t0003g0300 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(886): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(215): Show |
1 | a0001c0001t0003g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(224): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(255): Show |
1 | a0001c0001t0036g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(264): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1049): Show |
1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1058): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1151): Show |
1 | a0002c0002t0022g0219 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1160): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(2447): Show |
1 | a0001c0001t0028g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(2456): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(3655): Show |
1 | a0001c0001t0037g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(3664): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(2939): Show |
1 | a0001c0001t0005g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(2948): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(989): Show |
1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(998): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1611): Show |
1 | a0001c0001t0004g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1620): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1299): Show |
2 | a0001c0001t0015g0096a0001c0001t0015g0116 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.189-1044_189-1043i others(1308): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(991): Show |
1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1000): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1771): Show |
1 | a0001c0001t0004g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1780): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1513): Show |
1 | a0001c0001t0108g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1522): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747263
|
T | TGGGAGGC others(1687): Show |
1 | a0001c0001t0051g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1696): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747263 | |||||
| chr12:121747269
|
G | GCA | 4 | a0001c0001t0016g0308a0001c0001t0020g0122a0001c0001t0020g0126others(1): Show | 4 | HG01169.hp1 HG01255.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1056_189-1055i others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCACTGGG others(57): Show |
1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.189-1056_189-1055i others(66): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCACTGGG others(449): Show |
1 | a0001c0001t0097g0311 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.189-1056_189-1055i others(458): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCTGGGGT others(279): Show |
3 | a0001c0001t0001g0045a0001c0001t0008g0044a0001c0001t0106g0048 | 3 | HG02074.hp2 NA18940.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.189-1044_189-1043i others(288): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCTGGGGT others(1151): Show |
1 | a0001c0001t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1160): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCTGGGGT others(779): Show |
1 | a0001c0001t0015g0269 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(788): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCTGGGGT others(803): Show |
1 | a0001c0001t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(812): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCTGGGGT others(1055): Show |
1 | a0001c0001t0018g0024 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1064): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747269
|
G | GCTGGGGT others(1433): Show |
1 | a0001c0001t0012g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.189-1044_189-1043i others(1442): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747269 | |||||
| chr12:121747270
|
CTGGGGTA others(233): Show |
C | 14 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-1055_189-816de others(1): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747270 | ||||||
| chr12:121747270
|
CTGGGGTA others(315): Show |
C | 1 | a0001c0001t0020g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.189-1055_189-734de others(1): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747270 | ||||||
| chr12:121747270
|
CTGGGGTA others(415): Show |
C | 1 | a0001c0007t0026g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.189-1055_189-634de others(1): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747270 | ||||||
| chr12:121747270
|
CTGGGGTA others(475): Show |
C | 4 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(1): Show | 4 | HG01109.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1055_189-574de others(1): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747270 | ||||||
| chr12:121747270
|
CTGGGGTA others(617): Show |
C | 1 | a0001c0001t0026g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189-1055_189-432de others(1): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747270 | ||||||
| chr12:121747283
|
C | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0092others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.189-1043C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747283 | ||||||
| chr12:121747289
|
G | GCA | 4 | a0001c0001t0016g0308a0001c0001t0046g0067a0001c0001t0066g0138others(1): Show | 4 | HG01884.hp1 HG02071.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1036_189-1035i others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(683): Show |
1 | a0001c0001t0050g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(692): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(805): Show |
1 | a0001c0001t0072g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(814): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(723): Show |
2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.189-1024_189-1023i others(732): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(745): Show |
1 | a0001c0001t0005g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(754): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(3155): Show |
1 | a0001c0001t0028g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(3164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1777): Show |
1 | a0001c0001t0011g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1786): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(2095): Show |
1 | a0001c0001t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(2104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1503): Show |
1 | a0001c0001t0007g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1512): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(703): Show |
1 | a0001c0001t0006g0051 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(712): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(722): Show |
1 | a0001c0001t0069g0019 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(731): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(661): Show |
1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(670): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1233): Show |
1 | a0001c0001t0082g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1242): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(721): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(730): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(953): Show |
1 | a0001c0001t0025g0265 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(962): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(865): Show |
1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(874): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1955): Show |
1 | a0001c0001t0001g0313 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1964): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1531): Show |
1 | a0001c0001t0008g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1540): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(783): Show |
1 | a0001c0001t0083g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(792): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(805): Show |
1 | a0001c0001t0004g0203 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(814): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(805): Show |
2 | a0001c0001t0011g0002a0001c0001t0075g0181 | 2 | HG01975.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.189-1024_189-1023i others(814): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1859): Show |
1 | a0001c0001t0001g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1868): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1323): Show |
1 | a0001c0001t0015g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1332): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(933): Show |
1 | a0001c0001t0011g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(942): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(3372): Show |
1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(3381): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(2749): Show |
1 | a0001c0001t0022g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(2758): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1207): Show |
1 | a0001c0001t0002g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1216): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1079): Show |
1 | a0001c0001t0060g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1088): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(703): Show |
1 | a0001c0001t0049g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(712): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(701): Show |
2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.189-1024_189-1023i others(710): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(785): Show |
1 | a0001c0001t0005g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(794): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1197): Show |
1 | a0001c0001t0019g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1206): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(1161): Show |
1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(1170): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(825): Show |
1 | a0001c0001t0025g0264 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.189-1024_189-1023i others(834): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(783): Show |
1 | a0001c0001t0001g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.189-1024_189-1023i others(792): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | GCTGGGGT others(783): Show |
2 | a0001c0001t0005g0040a0001c0001t0056g0047 | 2 | HG00423.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.189-1024_189-1023i others(792): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747289
|
G | T | 5 | a0001c0001t0001g0185a0001c0001t0020g0122a0001c0001t0020g0126others(2): Show | 5 | HG01169.hp1 HG01255.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-1037G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747289 | ||||||
| chr12:121747289
|
GCTGGGGT others(15): Show |
G | 2 | a0001c0001t0079g0065a0002c0002t0001g0209 | 2 | HG00280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.189-1015_189-994de others(23): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747289 | |||||
| chr12:121747298
|
G | A | 3 | a0001c0001t0005g0042a0002c0002t0012g0080a0002c0002t0091g0283 | 3 | HG03130.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189-1028G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747298 | ||||||
| chr12:121747303
|
C | T | 238 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0092others(235): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.189-1023C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747303 | ||||||
| chr12:121747308
|
GGC | G | 4 | a0001c0001t0016g0308a0001c0001t0020g0122a0001c0001t0020g0126others(1): Show | 4 | HG01169.hp1 HG01255.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1017_189-1016d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747308 | ||||||
| chr12:121747309
|
G | T | 1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-1017G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747309 | ||||||
| chr12:121747309
|
GCA | G | 42 | a0001c0001t0001g0109a0001c0001t0002g0021a0001c0001t0002g0022others(39): Show | 42 | HG01099.hp1 HG01257.hp1 HG01516.hp1 others(39): Show |
intron_variant | MODIFIER | c.189-1015_189-1014d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747309 | |||||
| chr12:121747310
|
C | CTGGGGTA others(31): Show |
1 | a0002c0002t0022g0304 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.189-1016_189-1015i others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(967): Show |
1 | a0002c0002t0001g0194 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.189-1016_189-1015i others(976): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(987): Show |
1 | a0002c0002t0002g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.189-1016_189-1015i others(996): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(11): Show |
1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-1016_189-1015i others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(31): Show |
1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-1016_189-1015i others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(11): Show |
1 | a0002c0002t0012g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189-1016_189-1015i others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(215): Show |
1 | a0001c0001t0067g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.189-1016_189-1015i others(224): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(173): Show |
1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-1016_189-1015i others(182): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(743): Show |
1 | a0001c0001t0107g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.189-1016_189-1015i others(752): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(1425): Show |
1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.189-1016_189-1015i others(1434): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(2089): Show |
1 | a0001c0001t0011g0102 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189-1016_189-1015i others(2098): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747310
|
C | CTGGGGTA others(701): Show |
1 | a0001c0001t0001g0272 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.189-1016_189-1015i others(710): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747310 | ||||||
| chr12:121747311
|
A | ACTGGGGT others(13): Show |
4 | a0001c0001t0011g0206a0001c0001t0040g0259a0001c0001t0040g0260others(1): Show | 4 | HG00738.hp1 HG02258.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-1006_189-987du others(21): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(13): Show |
29 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0002g0139others(26): Show | 29 | HG00140.hp1 HG00621.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.189-1002_189-1001i others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(55): Show |
1 | a0001c0001t0003g0253 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.189-1002_189-1001i others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(33): Show |
1 | a0003c0003t0061g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.189-1002_189-1001i others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(53): Show |
7 | a0001c0001t0023g0297a0001c0001t0023g0301a0001c0001t0030g0159others(4): Show | 7 | HG00140.hp2 HG00558.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-1002_189-1001i others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(73): Show |
1 | a0001c0001t0017g0295 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.189-1002_189-1001i others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(93): Show |
1 | a0001c0001t0004g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.189-1002_189-1001i others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(353): Show |
1 | a0001c0001t0071g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.189-1002_189-1001i others(362): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | ACTGGGGT others(53): Show |
1 | a0001c0001t0003g0256 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.189-1002_189-1001i others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747311
|
A | G | 7 | a0001c0001t0001g0272a0001c0001t0011g0102a0001c0001t0067g0046others(4): Show | 7 | HG00621.hp1 HG01106.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-1015A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747311 | ||||||
| chr12:121747311
|
A | T | 9 | a0001c0001t0001g0268a0001c0001t0016g0308a0001c0001t0020g0122others(6): Show | 9 | HG00558.hp2 HG01169.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-1015A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747311 | ||||||
| chr12:121747311
|
ACTGGGGT others(33): Show |
A | 1 | a0001c0001t0046g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.189-986_189-947del others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747311 | |||||
| chr12:121747313
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.189-1013T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747313 | ||||||
| chr12:121747320
|
G | A | 7 | a0002c0002t0004g0103a0002c0002t0004g0224a0002c0002t0007g0178others(4): Show | 7 | HG01257.hp1 HG02027.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-1006G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747320 | ||||||
| chr12:121747320
|
G | GAAGGTGG others(33): Show |
3 | a0001c0001t0002g0057a0001c0001t0090g0294a0003c0003t0010g0072 | 3 | HG01123.hp1 HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.189-1002_189-1001i others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747320 | |||||
| chr12:121747320
|
G | GAAGGTGG others(93): Show |
1 | a0001c0001t0001g0006 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189-1002_189-1001i others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747320 | |||||
| chr12:121747320
|
G | GAAGGTGG others(95): Show |
2 | a0001c0001t0002g0136a0001c0001t0033g0135 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.189-1002_189-1001i others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747320 | |||||
| chr12:121747320
|
GAAGGCGG others(13): Show |
G | 2 | a0001c0001t0021g0288a0001c0001t0076g0287 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.189-986_189-967del others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747320 | |||||
| chr12:121747325
|
C | CGGGAGGC others(13): Show |
1 | a0001c0001t0103g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.189-987_189-986ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747325 | |||||
| chr12:121747325
|
C | T | 81 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0001g0109others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.189-1001C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747325 | ||||||
| chr12:121747331
|
G | GCA | 8 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0005g0059others(5): Show | 8 | HG00423.hp2 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-994_189-993ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747331 | |||||
| chr12:121747331
|
G | T | 5 | a0001c0001t0001g0185a0001c0001t0005g0042a0001c0001t0008g0115others(2): Show | 5 | HG01884.hp1 HG02165.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-995G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747331 | ||||||
| chr12:121747332
|
CTGGGGTA others(11): Show |
C | 2 | a0001c0001t0020g0122a0001c0001t0020g0126 | 2 | HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.189-993_189-976del others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747332 | ||||||
| chr12:121747332
|
CTGGGGTA others(353): Show |
C | 3 | a0001c0004t0003g0012a0001c0004t0099g0010a0001c0004t0100g0082 | 3 | HG02809.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.189-993_189-634del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747332 | ||||||
| chr12:121747337
|
G | GTAGAAGG others(707): Show |
1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-987_189-986ins others(714): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747337 | |||||
| chr12:121747340
|
A | AAAGGCGG others(113): Show |
1 | a0001c0001t0002g0147 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.189-873_189-754dup others(120): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747340 | |||||
| chr12:121747340
|
A | AAAGGTGG others(1195): Show |
1 | a0001c0001t0019g0034 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.189-982_189-981ins others(1202): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747340 | |||||
| chr12:121747340
|
A | AAAGGTGG others(1189): Show |
1 | a0001c0001t0019g0053 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.189-982_189-981ins others(1196): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747340 | |||||
| chr12:121747340
|
A | G | 212 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(209): Show | 213 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.189-986A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747340 | ||||||
| chr12:121747345
|
C | T | 57 | a0001c0001t0001g0109a0001c0001t0001g0185a0001c0001t0001g0313others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.189-981C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747345 | ||||||
| chr12:121747351
|
G | A | 2 | a0001c0001t0020g0122a0001c0001t0020g0126 | 2 | HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.189-975G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747351 | ||||||
| chr12:121747351
|
G | GCA | 5 | a0001c0001t0012g0074a0001c0001t0025g0264a0001c0001t0082g0073others(2): Show | 5 | HG00642.hp1 HG01167.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-974_189-973ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747351 | |||||
| chr12:121747351
|
G | GCTGGGGT others(521): Show |
1 | a0001c0001t0002g0028 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.189-956_189-955ins others(528): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747351 | |||||
| chr12:121747351
|
G | GCTGGGGT others(643): Show |
1 | a0001c0001t0006g0267 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.189-962_189-961ins others(650): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747351 | |||||
| chr12:121747351
|
G | GCTGGGGT others(623): Show |
1 | a0001c0001t0002g0030 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.189-962_189-961ins others(630): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747351 | |||||
| chr12:121747351
|
G | GCTGGGGT others(663): Show |
2 | a0001c0001t0029g0076a0001c0001t0029g0077 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.189-962_189-961ins others(670): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747351 | |||||
| chr12:121747351
|
G | T | 2 | a0001c0001t0016g0308a0002c0002t0022g0219 | 2 | HG01516.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.189-975G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747351 | ||||||
| chr12:121747360
|
G | A | 2 | a0001c0001t0016g0061a0001c0001t0036g0121 | 2 | HG02922.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.189-966G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747360 | ||||||
| chr12:121747365
|
C | T | 46 | a0001c0001t0001g0109a0001c0001t0001g0185a0001c0001t0002g0021others(43): Show | 46 | HG00280.hp1 HG01099.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.189-961C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747365 | ||||||
| chr12:121747371
|
G | GCA | 4 | a0001c0001t0016g0308a0001c0001t0019g0029a0002c0002t0012g0080others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-954_189-953ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(313): Show |
1 | a0001c0001t0042g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(320): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(293): Show |
1 | a0001c0009t0018g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(300): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(59): Show |
2 | a0001c0001t0015g0096a0001c0001t0015g0116 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.189-942_189-941ins others(66): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(313): Show |
1 | a0001c0001t0084g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.189-942_189-941ins others(320): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(645): Show |
1 | a0001c0001t0006g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.189-942_189-941ins others(652): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(1395): Show |
1 | a0001c0001t0010g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.189-942_189-941ins others(1402): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | GCTGGGGT others(981): Show |
1 | a0006c0008t0002g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.189-942_189-941ins others(988): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747371 | |||||
| chr12:121747371
|
G | T | 19 | a0001c0001t0002g0020a0001c0001t0005g0025a0001c0001t0006g0055others(16): Show | 19 | HG00558.hp2 HG02055.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.189-955G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747371 | ||||||
| chr12:121747380
|
G | A | 4 | a0001c0001t0005g0042a0001c0001t0021g0288a0001c0001t0076g0287others(1): Show | 4 | HG01243.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-946G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747380 | ||||||
| chr12:121747385
|
C | CGGGAGGC others(35): Show |
1 | a0002c0002t0003g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.189-934_189-933ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747385 | |||||
| chr12:121747385
|
C | CGGGAGGC others(137): Show |
1 | a0001c0001t0066g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.189-882_189-881ins others(144): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747385 | |||||
| chr12:121747385
|
C | T | 42 | a0001c0001t0001g0109a0001c0001t0001g0185a0001c0001t0002g0021others(39): Show | 42 | HG00280.hp1 HG01169.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.189-941C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747385 | ||||||
| chr12:121747391
|
G | GCA | 13 | a0001c0001t0001g0099a0001c0001t0005g0025a0001c0001t0010g0031others(10): Show | 13 | HG00423.hp2 HG01257.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.189-934_189-933ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCACTGGG others(375): Show |
1 | a0001c0001t0036g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.189-934_189-933ins others(382): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCACTGGG others(39): Show |
1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189-934_189-933ins others(46): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCACTGGG others(99): Show |
4 | a0001c0001t0006g0055a0001c0001t0006g0120a0001c0001t0027g0066others(1): Show | 4 | HG02080.hp1 NA18964.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-934_189-933ins others(106): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCACTGGG others(481): Show |
1 | a0001c0001t0002g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.189-934_189-933ins others(488): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCTGGGGT others(1179): Show |
1 | a0001c0001t0005g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.189-902_189-901ins others(1186): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCTGGGGT others(15): Show |
1 | a0002c0002t0065g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-922_189-921ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCTGGGGT others(537): Show |
1 | a0001c0001t0002g0026 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.189-922_189-921ins others(544): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCTGGGGT others(583): Show |
1 | a0001c0001t0002g0022 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.189-922_189-921ins others(590): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | GCTGGGGT others(35): Show |
1 | a0001c0001t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189-922_189-921ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747391
|
G | T | 1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-935G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747391 | ||||||
| chr12:121747391
|
GCTGGGGT others(175): Show |
G | 2 | a0001c0001t0021g0288a0001c0001t0076g0287 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.189-753_189-572del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747391 | |||||
| chr12:121747394
|
G | GGGGTAGA others(12): Show |
1 | a0001c0001t0033g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189-928_189-910dup others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747394 | |||||
| chr12:121747400
|
G | A | 3 | a0001c0001t0003g0247a0001c0001t0092g0124a0003c0003t0009g0070 | 3 | HG00140.hp1 HG03209.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.189-926G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747400 | ||||||
| chr12:121747405
|
C | T | 43 | a0001c0001t0001g0109a0001c0001t0001g0185a0001c0001t0001g0313others(40): Show | 43 | HG00280.hp1 HG00438.hp2 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.189-921C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747405 | ||||||
| chr12:121747411
|
G | GCA | 16 | a0001c0001t0001g0105a0001c0001t0002g0021a0001c0001t0002g0035others(13): Show | 16 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.189-914_189-913ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCACTGGG others(1199): Show |
2 | a0001c0001t0006g0049a0001c0001t0006g0050 | 2 | NA18950.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.189-914_189-913ins others(1206): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCACTGGG others(201): Show |
2 | a0001c0001t0001g0109a0001c0001t0025g0271 | 2 | HG01516.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.189-914_189-913ins others(208): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCACTGGG others(707): Show |
1 | a0001c0001t0081g0108 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.189-914_189-913ins others(714): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCACTGGG others(451): Show |
1 | a0001c0001t0041g0262 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.189-914_189-913ins others(458): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCTGGGGT others(203): Show |
1 | a0001c0001t0005g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189-894_189-893ins others(210): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCTGGGGT others(141): Show |
1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-882_189-881ins others(148): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | GCTGGGGT others(155): Show |
1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189-902_189-901ins others(162): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747411 | |||||
| chr12:121747411
|
G | T | 5 | a0001c0001t0036g0123a0002c0002t0001g0177a0002c0002t0001g0239others(2): Show | 5 | HG00558.hp2 HG00597.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-915G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747411 | ||||||
| chr12:121747417
|
G | A | 2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-909G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747417 | ||||||
| chr12:121747420
|
G | A | 1 | a0001c0001t0066g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.189-906G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747420 | ||||||
| chr12:121747425
|
C | T | 21 | a0001c0001t0001g0104a0001c0001t0001g0185a0001c0001t0005g0025others(18): Show | 21 | HG00438.hp2 HG01106.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.189-901C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747425 | ||||||
| chr12:121747425
|
C | TGGGAGGC others(1333): Show |
1 | a0001c0001t0025g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.189-902_189-901ins others(1340): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747425 | ||||||
| chr12:121747425
|
C | TGGGAGGC others(499): Show |
1 | a0001c0001t0001g0109 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.189-902_189-901ins others(506): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747425 | ||||||
| chr12:121747431
|
G | GCA | 14 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0005g0042others(11): Show | 14 | HG01978.hp1 HG02004.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-894_189-893ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCACTGGG others(171): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-894_189-893ins others(178): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(99): Show |
1 | a0001c0001t0004g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.189-842_189-841ins others(106): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(1177): Show |
1 | a0001c0001t0006g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.189-856_189-855ins others(1184): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(1177): Show |
1 | a0001c0001t0027g0273 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.189-856_189-855ins others(1184): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(497): Show |
1 | a0001c0001t0062g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.189-856_189-855ins others(504): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(463): Show |
1 | a0002c0002t0001g0234 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.189-856_189-855ins others(470): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(95): Show |
1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-882_189-881ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(2211): Show |
1 | a0001c0001t0072g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.189-882_189-881ins others(2218): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(827): Show |
1 | a0001c0001t0004g0203 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.189-882_189-881ins others(834): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | GCTGGGGT others(1031): Show |
2 | a0001c0001t0011g0002a0001c0001t0075g0181 | 2 | HG01975.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.189-882_189-881ins others(1038): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747431 | |||||
| chr12:121747431
|
G | T | 7 | a0001c0001t0001g0185a0001c0001t0041g0262a0001c0001t0102g0083others(4): Show | 7 | HG00558.hp2 HG00597.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-895G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747431 | ||||||
| chr12:121747445
|
C | CGGGAGGC others(607): Show |
1 | a0001c0001t0049g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189-862_189-861ins others(614): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747445 | |||||
| chr12:121747445
|
C | T | 21 | a0001c0001t0001g0185a0001c0001t0005g0025a0001c0001t0006g0033others(18): Show | 21 | HG01106.hp1 HG01169.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.189-881C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747445 | ||||||
| chr12:121747450
|
G | GTCTGGGG others(159): Show |
1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.189-876_189-875ins others(166): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747450 | ||||||
| chr12:121747451
|
G | A | 1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.189-875G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747451 | ||||||
| chr12:121747451
|
G | GCA | 6 | a0001c0001t0001g0006a0001c0001t0001g0105a0001c0001t0005g0025others(3): Show | 6 | HG01358.hp1 HG02155.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-874_189-873ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCACTGGG others(191): Show |
1 | a0001c0001t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.189-874_189-873ins others(198): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCACTGGG others(37): Show |
1 | a0002c0002t0008g0292 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.189-874_189-873ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCACTGGG others(117): Show |
2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-874_189-873ins others(124): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCTGGGGT others(77): Show |
1 | a0001c0001t0028g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.189-814_189-813ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCTGGGGT others(491): Show |
1 | a0001c0001t0015g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.189-842_189-841ins others(498): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCTGGGGT others(521): Show |
1 | a0001c0001t0002g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189-856_189-855ins others(528): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCTGGGGT others(521): Show |
1 | a0001c0001t0010g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.189-856_189-855ins others(528): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCTGGGGT others(411): Show |
1 | a0001c0001t0054g0093 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.189-862_189-861ins others(418): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | GCTGGGGT others(371): Show |
1 | a0001c0001t0057g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-862_189-861ins others(378): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747451 | |||||
| chr12:121747451
|
G | T | 6 | a0001c0001t0016g0308a0001c0001t0109g0182a0002c0002t0001g0177others(3): Show | 6 | HG00558.hp2 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-875G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747451 | ||||||
| chr12:121747465
|
C | CGGGAGGC others(441): Show |
1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-854_189-853ins others(448): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747465 | |||||
| chr12:121747465
|
C | CGGGAGTC others(283): Show |
1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-856_189-855ins others(290): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747465 | |||||
| chr12:121747465
|
C | T | 20 | a0001c0001t0001g0272a0001c0001t0005g0025a0001c0001t0005g0081others(17): Show | 20 | HG00544.hp2 HG00621.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.189-861C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747465 | ||||||
| chr12:121747470
|
G | GTCTGGGG others(159): Show |
1 | a0002c0002t0012g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.189-856_189-855ins others(166): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747470 | ||||||
| chr12:121747470
|
G | GTCTGGGG others(321): Show |
1 | a0002c0002t0002g0192 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.189-856_189-855ins others(328): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747470 | ||||||
| chr12:121747471
|
G | A | 2 | a0002c0002t0002g0192a0002c0002t0012g0175 | 2 | HG02040.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.189-855G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747471 | ||||||
| chr12:121747471
|
G | GCA | 5 | a0001c0001t0001g0092a0001c0001t0005g0081a0001c0001t0007g0266others(2): Show | 5 | HG01346.hp1 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-854_189-853ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCACTGGG others(309): Show |
1 | a0001c0001t0051g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.189-854_189-853ins others(316): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCACTGGG others(79): Show |
1 | a0001c0001t0083g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189-854_189-853ins others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCACTGGG others(121): Show |
1 | a0001c0001t0041g0261 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.189-854_189-853ins others(128): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCACTGGG others(35): Show |
1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-854_189-853ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(369): Show |
1 | a0001c0001t0108g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.189-822_189-821ins others(376): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(57): Show |
1 | a0001c0001t0025g0265 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189-822_189-821ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(1033): Show |
1 | a0002c0002t0014g0228 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(1040): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(321): Show |
1 | a0002c0002t0001g0170 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189-836_189-835ins others(328): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(727): Show |
1 | a0002c0002t0038g0230 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.189-836_189-835ins others(734): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(913): Show |
1 | a0002c0002t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(920): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(727): Show |
1 | a0002c0002t0007g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(734): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(747): Show |
2 | a0002c0002t0017g0258a0002c0002t0017g0279 | 2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.189-836_189-835ins others(754): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | GCTGGGGT others(563): Show |
1 | a0002c0002t0015g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(570): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747471 | |||||
| chr12:121747471
|
G | T | 32 | a0001c0001t0001g0185a0001c0001t0002g0035a0001c0001t0002g0112others(29): Show | 32 | HG00558.hp2 HG01884.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.189-855G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747471 | ||||||
| chr12:121747480
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189-846G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747480 | ||||||
| chr12:121747485
|
C | CGGGAGGC others(15): Show |
1 | a0002c0002t0003g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.189-834_189-833ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGGC others(159): Show |
1 | a0002c0002t0012g0174 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-834_189-833ins others(166): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(35): Show |
3 | a0002c0002t0007g0200a0002c0002t0012g0163a0002c0002t0086g0291 | 3 | HG03041.hp2 HG03516.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.189-836_189-835ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(55): Show |
1 | a0002c0002t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.189-836_189-835ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(55): Show |
20 | a0002c0002t0001g0238a0002c0002t0001g0243a0002c0002t0001g0249others(17): Show | 21 | HG00438.hp1 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.189-836_189-835ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(625): Show |
1 | a0002c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189-836_189-835ins others(632): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(523): Show |
1 | a0002c0002t0004g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(530): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(645): Show |
1 | a0002c0002t0031g0303 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(652): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | CGGGAGTC others(645): Show |
1 | a0002c0002t0013g0037 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(652): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747485 | |||||
| chr12:121747485
|
C | T | 25 | a0001c0001t0001g0185a0001c0001t0001g0272a0001c0001t0002g0023others(22): Show | 25 | HG00621.hp1 HG01169.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.189-841C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747485 | ||||||
| chr12:121747490
|
G | GTCTGGGG others(727): Show |
2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.189-836_189-835ins others(734): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747490 | ||||||
| chr12:121747490
|
G | GTCTGGGG others(667): Show |
1 | a0002c0002t0058g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(674): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747490 | ||||||
| chr12:121747490
|
G | GTCTGGGG others(565): Show |
1 | a0002c0002t0004g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(572): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747490 | ||||||
| chr12:121747490
|
G | GTCTGGGG others(1259): Show |
1 | a0002c0002t0002g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.189-836_189-835ins others(1266): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747490 | ||||||
| chr12:121747490
|
G | GTCTGGGG others(853): Show |
1 | a0002c0002t0004g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.189-836_189-835ins others(860): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747490 | ||||||
| chr12:121747490
|
G | GTCTGGGG others(727): Show |
1 | a0002c0002t0013g0038 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.189-836_189-835ins others(734): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747490 | ||||||
| chr12:121747491
|
G | A | 6 | a0002c0002t0001g0236a0002c0002t0001g0237a0002c0002t0004g0187others(3): Show | 6 | HG00738.hp2 HG01071.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-835G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747491 | ||||||
| chr12:121747491
|
G | GCA | 21 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0003g0107others(18): Show | 21 | HG00621.hp1 HG01934.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.189-834_189-833ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCACTGGG others(37): Show |
1 | a0002c0002t0018g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.189-834_189-833ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCACTGGG others(227): Show |
1 | a0001c0001t0010g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.189-834_189-833ins others(234): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCACTGGG others(335): Show |
1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189-834_189-833ins others(342): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCACTGGG others(481): Show |
1 | a0001c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.189-834_189-833ins others(488): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCTGGGGT others(940): Show |
1 | a0001c0001t0022g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.189-814_189-813ins others(947): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCTGGGGT others(1539): Show |
1 | a0001c0001t0106g0048 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.189-782_189-781ins others(1546): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | GCTGGGGT others(13): Show |
1 | a0002c0002t0089g0244 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747491 | |||||
| chr12:121747491
|
G | T | 41 | a0001c0001t0005g0042a0001c0001t0016g0308a0001c0001t0041g0261others(38): Show | 41 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.189-835G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747491 | ||||||
| chr12:121747505
|
C | CGGGAGGC others(15): Show |
2 | a0002c0002t0001g0239a0002c0002t0003g0087 | 2 | HG02056.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.189-814_189-813ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747505 | |||||
| chr12:121747505
|
C | CGGGAGGC others(1707): Show |
1 | a0001c0001t0005g0040 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.189-814_189-813ins others(1714): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747505 | |||||
| chr12:121747505
|
C | CGGGAGGC others(13): Show |
1 | a0002c0002t0012g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.189-802_189-801ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747505 | |||||
| chr12:121747505
|
C | CGGGAGTC others(157): Show |
3 | a0002c0002t0008g0221a0002c0002t0008g0293a0002c0002t0095g0245 | 3 | HG00597.hp1 HG02155.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.189-816_189-815ins others(164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747505 | |||||
| chr12:121747505
|
C | CGGGAGTC others(93): Show |
1 | a0002c0002t0096g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747505 | |||||
| chr12:121747505
|
C | T | 60 | a0001c0001t0001g0104a0001c0001t0001g0185a0001c0001t0001g0272others(57): Show | 61 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.189-821C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747505 | ||||||
| chr12:121747505
|
C | TGGGAGGC others(313): Show |
3 | a0001c0001t0006g0120a0001c0001t0027g0066a0001c0001t0052g0054 | 3 | HG02080.hp1 NA18994.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.189-822_189-821ins others(320): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747505 | ||||||
| chr12:121747505
|
C | TGGGAGGC others(433): Show |
1 | a0001c0001t0006g0055 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.189-822_189-821ins others(440): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747505 | ||||||
| chr12:121747505
|
C | TGGGAGGC others(1033): Show |
1 | a0002c0002t0014g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.189-822_189-821ins others(1040): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747505 | ||||||
| chr12:121747505
|
C | TGGGAGGC others(1053): Show |
1 | a0002c0002t0014g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.189-822_189-821ins others(1060): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747505 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(707): Show |
1 | a0002c0002t0010g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(714): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(847): Show |
2 | a0002c0002t0024g0197a0002c0002t0024g0207 | 2 | HG00735.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.189-816_189-815ins others(854): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(769): Show |
1 | a0002c0002t0093g0212 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(776): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(727): Show |
1 | a0002c0002t0013g0039 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(734): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(687): Show |
1 | a0002c0002t0001g0213 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.189-816_189-815ins others(694): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(687): Show |
1 | a0002c0002t0004g0218 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.189-816_189-815ins others(694): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(687): Show |
1 | a0002c0002t0007g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(694): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(645): Show |
1 | a0002c0002t0007g0220 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.189-816_189-815ins others(652): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747510
|
G | GTCTGGGG others(707): Show |
1 | a0002c0002t0048g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.189-816_189-815ins others(714): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747510 | ||||||
| chr12:121747511
|
G | A | 24 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(21): Show | 24 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.189-815G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747511 | ||||||
| chr12:121747511
|
G | GCA | 25 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0272others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-814_189-813ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCACTGGG others(79): Show |
1 | a0001c0001t0001g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.189-814_189-813ins others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCACTGGG others(101): Show |
1 | a0001c0001t0056g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.189-814_189-813ins others(108): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCACTGGG others(205): Show |
1 | a0002c0002t0003g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.189-814_189-813ins others(212): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCACTGGG others(139): Show |
1 | a0002c0002t0104g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.189-814_189-813ins others(146): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCACTGGG others(547): Show |
1 | a0002c0002t0008g0223 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.189-814_189-813ins others(554): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCACTGGG others(443): Show |
1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-814_189-813ins others(450): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCTGGGGT others(77): Show |
1 | a0002c0002t0012g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.189-802_189-801ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | GCTGGGGT others(97): Show |
2 | a0002c0002t0034g0001a0002c0002t0086g0291 | 2 | HG01258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.189-802_189-801ins others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747511 | |||||
| chr12:121747511
|
G | T | 20 | a0001c0001t0015g0269a0001c0001t0016g0308a0001c0001t0020g0122others(17): Show | 20 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-815G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747511 | ||||||
| chr12:121747512
|
CTGGGGTA others(213): Show |
C | 1 | a0001c0001t0046g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.189-813_189-594del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747512 | ||||||
| chr12:121747520
|
G | A | 1 | a0003c0003t0009g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189-806G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747520 | ||||||
| chr12:121747520
|
G | GAAGGCGG others(35): Show |
1 | a0001c0001t0003g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747520 | |||||
| chr12:121747525
|
C | CGGGAGTC others(913): Show |
1 | a0002c0002t0007g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.189-796_189-795ins others(920): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747525 | |||||
| chr12:121747525
|
C | CGGGAGTC others(139): Show |
1 | a0002c0002t0016g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-796_189-795ins others(146): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747525 | |||||
| chr12:121747525
|
C | T | 81 | a0001c0001t0001g0118a0001c0001t0001g0185a0001c0001t0002g0023others(78): Show | 81 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.189-801C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747525 | ||||||
| chr12:121747530
|
G | GGCACTGG others(143): Show |
1 | a0001c0001t0097g0311 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(150): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747530 | |||||
| chr12:121747530
|
G | GGCTGGGG others(597): Show |
1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.189-782_189-781ins others(604): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747530 | |||||
| chr12:121747531
|
G | GCA | 12 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0025others(9): Show | 12 | HG01169.hp2 HG01891.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-794_189-793ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(101): Show |
1 | a0002c0002t0018g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(108): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(205): Show |
1 | a0001c0001t0002g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(212): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(57): Show |
1 | a0002c0002t0003g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.189-794_189-793ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(77): Show |
1 | a0002c0002t0001g0199 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(807): Show |
1 | a0002c0002t0024g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(814): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(729): Show |
1 | a0002c0002t0001g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(736): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(363): Show |
1 | a0002c0002t0004g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189-794_189-793ins others(370): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(765): Show |
1 | a0002c0002t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.189-794_189-793ins others(772): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(545): Show |
2 | a0002c0002t0001g0201a0002c0002t0088g0160 | 2 | HG02071.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.189-794_189-793ins others(552): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(749): Show |
1 | a0002c0002t0007g0202 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.189-794_189-793ins others(756): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(769): Show |
1 | a0002c0002t0004g0090 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-794_189-793ins others(776): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(849): Show |
1 | a0002c0002t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.189-794_189-793ins others(856): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCACTGGG others(1035): Show |
1 | a0002c0002t0085g0205 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.189-794_189-793ins others(1042): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCTGGGGT others(15): Show |
8 | a0002c0002t0001g0195a0002c0002t0004g0128a0002c0002t0007g0186others(5): Show | 8 | HG01071.hp2 HG01106.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-782_189-781ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCTGGGGT others(57): Show |
2 | a0002c0002t0034g0001a0002c0002t0077g0257 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.189-782_189-781ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCTGGGGT others(199): Show |
1 | a0002c0002t0008g0309 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.189-782_189-781ins others(206): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | GCTGGGGT others(645): Show |
1 | a0002c0002t0038g0216 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.189-782_189-781ins others(652): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747531 | |||||
| chr12:121747531
|
G | T | 27 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(24): Show | 27 | HG01167.hp2 HG02027.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.189-795G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747531 | ||||||
| chr12:121747537
|
G | A | 2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-789G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747537 | ||||||
| chr12:121747545
|
C | T | 75 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0272others(72): Show | 75 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.189-781C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747545 | ||||||
| chr12:121747545
|
C | TGGGAGGC others(35): Show |
1 | a0002c0002t0007g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.189-782_189-781ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747545 | ||||||
| chr12:121747545
|
C | TGGGAGGC others(75): Show |
1 | a0002c0002t0004g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.189-782_189-781ins others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747545 | ||||||
| chr12:121747551
|
G | GCA | 21 | a0001c0001t0002g0028a0001c0001t0002g0030a0001c0001t0005g0081others(18): Show | 21 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.189-774_189-773ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCACTGGG others(61): Show |
1 | a0001c0001t0006g0267 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.189-774_189-773ins others(68): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCACTGGG others(59): Show |
1 | a0001c0001t0010g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.189-774_189-773ins others(66): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCACTGGG others(439): Show |
1 | a0001c0001t0101g0007 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.189-774_189-773ins others(446): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCACTGGG others(563): Show |
1 | a0001c0001t0011g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.189-774_189-773ins others(570): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCACTGGG others(541): Show |
1 | a0001c0001t0003g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.189-774_189-773ins others(548): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCTGGGGT others(981): Show |
1 | a0001c0001t0004g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(988): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCTGGGGT others(33): Show |
2 | a0002c0002t0004g0103a0002c0002t0105g0097 | 2 | HG02129.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.189-756_189-755ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCTGGGGT others(689): Show |
1 | a0001c0001t0008g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189-762_189-761ins others(696): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | GCTGGGGT others(665): Show |
1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-762_189-761ins others(672): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747551 | |||||
| chr12:121747551
|
G | T | 30 | a0001c0001t0001g0185a0001c0001t0005g0008a0001c0001t0005g0149others(27): Show | 30 | HG00544.hp1 HG01167.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.189-775G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747551 | ||||||
| chr12:121747565
|
C | CGGGAGGC others(53): Show |
1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747565 | |||||
| chr12:121747565
|
C | CGGGAGGC others(35): Show |
1 | a0001c0001t0015g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747565 | |||||
| chr12:121747565
|
C | CGGGAGGC others(2619): Show |
1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(2626): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747565 | |||||
| chr12:121747565
|
C | CGGGAGTC others(385): Show |
1 | a0002c0002t0003g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.189-756_189-755ins others(392): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747565 | |||||
| chr12:121747565
|
C | T | 105 | a0001c0001t0001g0185a0001c0001t0001g0272a0001c0001t0002g0022others(102): Show | 105 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.189-761C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747565 | ||||||
| chr12:121747570
|
GGC | G | 3 | a0001c0001t0004g0217a0001c0001t0030g0162a0002c0002t0001g0209 | 3 | HG00140.hp2 HG00280.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.189-755_189-754del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747570 | ||||||
| chr12:121747571
|
G | T | 6 | a0001c0001t0003g0248a0001c0001t0017g0295a0001c0001t0090g0294others(3): Show | 6 | HG00544.hp1 HG01123.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-755G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747571 | ||||||
| chr12:121747571
|
GCA | G | 73 | a0001c0001t0001g0129a0001c0001t0001g0277a0001c0001t0001g0313others(70): Show | 74 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.189-753_189-752del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747571 | |||||
| chr12:121747572
|
C | CTGGGGTA others(277): Show |
1 | a0003c0003t0061g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(284): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(11): Show |
4 | a0001c0001t0017g0295a0001c0001t0025g0265a0001c0001t0066g0138others(1): Show | 4 | HG01123.hp1 HG01934.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-754_189-753ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(177): Show |
1 | a0002c0002t0045g0043 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(184): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(555): Show |
1 | a0001c0001t0003g0300 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(562): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(311): Show |
1 | a0001c0001t0001g0006 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(318): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(291): Show |
1 | a0001c0001t0003g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(291): Show |
2 | a0004c0005t0064g0282a0004c0005t0073g0281 | 2 | NA18951.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.189-754_189-753ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(291): Show |
1 | a0001c0001t0036g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(211): Show |
1 | a0001c0001t0003g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(218): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(231): Show |
1 | a0001c0001t0001g0179 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(238): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(291): Show |
1 | a0001c0001t0006g0172 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(851): Show |
1 | a0001c0001t0067g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(858): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(231): Show |
1 | a0001c0001t0103g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(238): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(251): Show |
1 | a0001c0001t0087g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(258): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(331): Show |
1 | a0001c0001t0008g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(338): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(751): Show |
1 | a0001c0001t0074g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(758): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(311): Show |
1 | a0001c0001t0059g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(318): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(711): Show |
1 | a0001c0001t0023g0298 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(718): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(91): Show |
1 | a0001c0001t0032g0142 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(98): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(271): Show |
1 | a0001c0001t0001g0176 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(278): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(291): Show |
1 | a0001c0001t0013g0168 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(111): Show |
2 | a0001c0001t0018g0140a0001c0001t0032g0141 | 2 | HG00558.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.189-754_189-753ins others(118): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(471): Show |
1 | a0001c0001t0005g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(478): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(151): Show |
1 | a0001c0001t0002g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(158): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(291): Show |
1 | a0001c0001t0011g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(1167): Show |
1 | a0001c0001t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(1174): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(1009): Show |
1 | a0002c0002t0004g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(1016): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(909): Show |
1 | a0002c0002t0007g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(916): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(51): Show |
2 | a0001c0001t0023g0297a0001c0001t0023g0301 | 2 | HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.189-754_189-753ins others(58): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(251): Show |
1 | a0001c0001t0004g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(258): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(171): Show |
2 | a0001c0001t0002g0136a0001c0001t0033g0135 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.189-754_189-753ins others(178): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(373): Show |
1 | a0001c0001t0003g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(380): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(95): Show |
1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(33): Show |
13 | a0001c0001t0001g0118a0002c0002t0001g0193a0002c0002t0001g0213others(10): Show | 13 | HG00438.hp1 HG00642.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.189-754_189-753ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(53): Show |
1 | a0002c0002t0007g0220 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(113): Show |
1 | a0002c0002t0007g0200 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(120): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(55): Show |
1 | a0001c0001t0002g0026 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.189-754_189-753ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747572
|
C | CTGGGGTA others(159): Show |
1 | a0002c0002t0003g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.189-754_189-753ins others(166): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747572 | ||||||
| chr12:121747573
|
A | ACTGGGGT others(53): Show |
2 | a0001c0001t0002g0147a0001c0001t0084g0146 | 2 | HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.189-519_189-460dup others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(1861): Show |
1 | a0001c0001t0056g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.189-720_189-719ins others(1868): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(341): Show |
1 | a0002c0002t0016g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-740_189-739ins others(348): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(301): Show |
1 | a0002c0002t0053g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.189-740_189-739ins others(308): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(95): Show |
1 | a0002c0002t0015g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.189-740_189-739ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(137): Show |
1 | a0002c0002t0008g0292 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.189-740_189-739ins others(144): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(997): Show |
1 | a0002c0002t0014g0127 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.189-740_189-739ins others(1004): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | ACTGGGGT others(807): Show |
1 | a0002c0002t0013g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.189-740_189-739ins others(814): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747573 | |||||
| chr12:121747573
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0118others(35): Show | 38 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.189-753A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747573 | ||||||
| chr12:121747573
|
A | T | 22 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0004g0217others(19): Show | 22 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.189-753A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747573 | ||||||
| chr12:121747582
|
G | GAAGGCGG others(13): Show |
3 | a0003c0003t0002g0284a0003c0003t0002g0285a0003c0003t0010g0068 | 3 | HG02615.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.189-725_189-724ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747582 | |||||
| chr12:121747587
|
C | CGGGAGGC others(159): Show |
1 | a0001c0001t0008g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.189-732_189-731ins others(166): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747587 | |||||
| chr12:121747587
|
C | T | 66 | a0001c0001t0001g0118a0001c0001t0001g0185a0001c0001t0002g0020others(63): Show | 66 | HG00544.hp1 HG00735.hp1 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.189-739C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747587 | ||||||
| chr12:121747587
|
C | TGGGAGGC others(137): Show |
1 | a0002c0002t0089g0244 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.189-740_189-739ins others(144): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747587 | ||||||
| chr12:121747593
|
G | A | 1 | a0001c0001t0020g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.189-733G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747593 | ||||||
| chr12:121747593
|
G | GCA | 25 | a0001c0001t0001g0118a0001c0001t0002g0020a0001c0001t0002g0022others(22): Show | 25 | HG00642.hp1 HG00735.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.189-732_189-731ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(55): Show |
1 | a0002c0002t0013g0037 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.189-680_189-679ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(35): Show |
1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.189-700_189-699ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(15): Show |
1 | a0002c0002t0001g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.189-720_189-719ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(183): Show |
1 | a0001c0001t0018g0024 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.189-720_189-719ins others(190): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(225): Show |
1 | a0001c0001t0010g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.189-720_189-719ins others(232): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(665): Show |
1 | a0001c0001t0069g0019 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.189-720_189-719ins others(672): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | GCTGGGGT others(55): Show |
1 | a0002c0002t0001g0201 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.189-720_189-719ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747593 | |||||
| chr12:121747593
|
G | T | 20 | a0001c0001t0002g0139a0001c0001t0015g0269a0001c0001t0016g0308others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-733G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747593 | ||||||
| chr12:121747596
|
G | GGGGTAGA others(435): Show |
1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-700_189-699ins others(442): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747596 | |||||
| chr12:121747602
|
G | A | 1 | a0003c0003t0002g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.189-724G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747602 | ||||||
| chr12:121747607
|
C | T | 69 | a0001c0001t0001g0099a0001c0001t0001g0185a0001c0001t0001g0272others(66): Show | 70 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.189-719C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747607 | ||||||
| chr12:121747613
|
G | GCA | 15 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0003g0254others(12): Show | 15 | HG00280.hp1 HG00544.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.189-712_189-711ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCACTGGG others(665): Show |
1 | a0001c0001t0050g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189-712_189-711ins others(672): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCACTGGG others(553): Show |
1 | a0001c0001t0005g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.189-712_189-711ins others(560): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCACTGGG others(163): Show |
1 | a0006c0008t0002g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.189-712_189-711ins others(170): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCACTGGG others(17): Show |
1 | a0001c0001t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.189-712_189-711ins others(24): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCACTGGG others(57): Show |
1 | a0001c0001t0060g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.189-712_189-711ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCAGGGGT others(119): Show |
1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-712_189-711ins others(126): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | GCTGGGGT others(623): Show |
1 | a0002c0002t0022g0304 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.189-700_189-699ins others(630): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747613 | |||||
| chr12:121747613
|
G | T | 22 | a0001c0001t0001g0079a0001c0001t0005g0008a0001c0001t0005g0149others(19): Show | 22 | HG01167.hp1 HG01257.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.189-713G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747613 | ||||||
| chr12:121747613
|
G | TCTGGGGT others(13): Show |
1 | a0002c0002t0022g0219 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.189-714_189-713ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747613 | ||||||
| chr12:121747614
|
CTGGGGTA others(231): Show |
C | 1 | a0001c0001t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.189-711_189-474del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747614 | ||||||
| chr12:121747615
|
T | A | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189-711T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747615 | ||||||
| chr12:121747624
|
A | AGGCGGGA others(95): Show |
1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-680_189-679ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747624 | |||||
| chr12:121747627
|
C | CGGGAGGC others(13): Show |
1 | a0001c0001t0011g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189-680_189-679ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747627 | |||||
| chr12:121747627
|
C | CGGGAGGC others(1527): Show |
1 | a0001c0001t0007g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.189-680_189-679ins others(1534): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747627 | |||||
| chr12:121747627
|
C | T | 76 | a0001c0001t0001g0185a0001c0001t0001g0313a0001c0001t0002g0020others(73): Show | 77 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.189-699C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747627 | ||||||
| chr12:121747633
|
G | GCA | 30 | a0001c0001t0001g0313a0001c0001t0002g0020a0001c0001t0002g0023others(27): Show | 30 | HG01106.hp1 HG01169.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.189-692_189-691ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCACTGGG others(923): Show |
1 | a0001c0001t0001g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.189-692_189-691ins others(930): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCACTGGG others(123): Show |
1 | a0001c0001t0028g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-692_189-691ins others(130): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCACTGGG others(39): Show |
1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189-692_189-691ins others(46): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCACTGGG others(79): Show |
1 | a0002c0002t0065g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-692_189-691ins others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(113): Show |
1 | a0002c0002t0007g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.189-594_189-593ins others(120): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(73): Show |
1 | a0001c0001t0040g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.189-674_189-673ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(59): Show |
1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-680_189-679ins others(66): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(229): Show |
1 | a0001c0001t0002g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189-680_189-679ins others(236): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(291): Show |
2 | a0001c0001t0001g0109a0001c0001t0081g0108 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.189-680_189-679ins others(298): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(57): Show |
2 | a0002c0002t0004g0103a0002c0002t0105g0097 | 2 | HG02129.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.189-680_189-679ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(179): Show |
1 | a0002c0002t0012g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189-680_189-679ins others(186): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(317): Show |
1 | a0002c0002t0001g0234 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.189-680_189-679ins others(324): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | GCTGGGGT others(177): Show |
1 | a0002c0002t0001g0199 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.189-680_189-679ins others(184): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747633 | |||||
| chr12:121747633
|
G | T | 15 | a0001c0001t0001g0079a0001c0001t0001g0129a0001c0001t0001g0277others(12): Show | 15 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.189-693G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747633 | ||||||
| chr12:121747647
|
C | CGGGAGGC others(97): Show |
1 | a0001c0001t0006g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.189-660_189-659ins others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747647 | |||||
| chr12:121747647
|
C | T | 63 | a0001c0001t0001g0185a0001c0001t0001g0272a0001c0001t0002g0020others(60): Show | 63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.189-679C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747647 | ||||||
| chr12:121747647
|
C | TGGGAGGC others(55): Show |
1 | a0002c0002t0012g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189-680_189-679ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747647 | ||||||
| chr12:121747647
|
CGGGAGGC others(319): Show |
C | 2 | a0001c0001t0020g0122a0001c0001t0020g0126 | 2 | HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.189-659_189-334del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747647 | |||||
| chr12:121747653
|
G | GCA | 16 | a0001c0001t0002g0020a0001c0001t0010g0032a0001c0001t0011g0206others(13): Show | 16 | HG01099.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.189-672_189-671ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCACTGGG others(495): Show |
1 | a0001c0001t0025g0264 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.189-672_189-671ins others(502): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCACTGGG others(99): Show |
1 | a0002c0002t0004g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189-672_189-671ins others(106): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCACTGGG others(327): Show |
1 | a0001c0001t0041g0262 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.189-672_189-671ins others(334): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(13): Show |
1 | a0002c0002t0002g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.189-654_189-653ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(53): Show |
2 | a0002c0002t0004g0204a0002c0002t0013g0038 | 2 | HG03491.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.189-654_189-653ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(93): Show |
1 | a0001c0001t0040g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.189-654_189-653ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(15): Show |
2 | a0002c0002t0031g0303a0002c0002t0086g0291 | 2 | HG02148.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.189-660_189-659ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(37): Show |
1 | a0001c0001t0001g0272 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.189-660_189-659ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(57): Show |
2 | a0001c0001t0001g0185a0001c0001t0097g0311 | 2 | HG03927.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.189-660_189-659ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(77): Show |
2 | a0001c0001t0005g0059a0001c0001t0005g0060 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.189-660_189-659ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | GCTGGGGT others(57): Show |
2 | a0001c0001t0027g0066a0001c0001t0052g0054 | 2 | NA18994.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.189-660_189-659ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747653 | |||||
| chr12:121747653
|
G | T | 41 | a0001c0001t0001g0079a0001c0001t0001g0129a0001c0001t0001g0277others(38): Show | 41 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.189-673G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747653 | ||||||
| chr12:121747656
|
G | GGGGTAGA others(150): Show |
1 | a0001c0001t0033g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189-648_189-647ins others(157): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747656 | |||||
| chr12:121747667
|
C | T | 74 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0268others(71): Show | 74 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.189-659C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747667 | ||||||
| chr12:121747673
|
G | GCA | 43 | a0001c0001t0001g0129a0001c0001t0001g0277a0001c0001t0001g0313others(40): Show | 43 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.189-652_189-651ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCACTGGG others(187): Show |
1 | a0001c0001t0006g0049 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.189-652_189-651ins others(194): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCACTGGG others(75): Show |
1 | a0001c0001t0002g0026 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.189-652_189-651ins others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCACTGGG others(411): Show |
1 | a0001c0001t0005g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189-652_189-651ins others(418): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCACTGGG others(525): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-652_189-651ins others(532): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCTGGGGT others(121): Show |
1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-634_189-633ins others(128): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCTGGGGT others(95): Show |
1 | a0002c0002t0001g0170 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189-640_189-639ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | GCTGGGGT others(319): Show |
1 | a0001c0001t0019g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.189-640_189-639ins others(326): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747673 | |||||
| chr12:121747673
|
G | T | 32 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0255others(29): Show | 32 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.189-653G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747673 | ||||||
| chr12:121747687
|
C | CGGGAGGC others(389): Show |
1 | a0001c0001t0041g0261 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.189-620_189-619ins others(396): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747687 | |||||
| chr12:121747687
|
C | T | 68 | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0001t0001g0185others(65): Show | 68 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.189-639C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747687 | ||||||
| chr12:121747688
|
G | T | 1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-638G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747688 | ||||||
| chr12:121747689
|
G | A | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189-637G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747689 | ||||||
| chr12:121747693
|
G | A | 4 | a0001c0004t0003g0012a0001c0004t0099g0010a0001c0004t0100g0082others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-633G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747693 | ||||||
| chr12:121747693
|
G | GCA | 35 | a0001c0001t0001g0313a0001c0001t0002g0023a0001c0001t0002g0028others(32): Show | 35 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.189-632_189-631ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCACTGGG others(165): Show |
3 | a0001c0001t0006g0050a0001c0001t0006g0056a0001c0001t0027g0273 | 3 | NA18973.hp2 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.189-632_189-631ins others(172): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCACTGGG others(229): Show |
1 | a0001c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.189-632_189-631ins others(236): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCACTGGG others(119): Show |
1 | a0002c0002t0003g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.189-632_189-631ins others(126): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(15): Show |
4 | a0001c0001t0002g0136a0001c0001t0033g0135a0001c0001t0036g0121others(1): Show | 4 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-612_189-611ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(121): Show |
1 | a0001c0001t0106g0048 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.189-612_189-611ins others(128): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(219): Show |
1 | a0001c0001t0010g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.189-560_189-559ins others(226): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(305): Show |
1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189-594_189-593ins others(312): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(113): Show |
1 | a0001c0001t0066g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.189-614_189-613ins others(120): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(265): Show |
1 | a0001c0001t0057g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-614_189-613ins others(272): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(15): Show |
1 | a0001c0001t0001g0272 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.189-620_189-619ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(117): Show |
2 | a0002c0002t0001g0195a0002c0002t0031g0091 | 2 | HG01106.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.189-620_189-619ins others(124): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(181): Show |
1 | a0002c0002t0014g0196 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.189-620_189-619ins others(188): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(223): Show |
1 | a0002c0002t0004g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.189-620_189-619ins others(230): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(1765): Show |
1 | a0001c0001t0029g0076 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.189-620_189-619ins others(1772): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(1603): Show |
1 | a0001c0001t0029g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.189-620_189-619ins others(1610): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | GCTGGGGT others(35): Show |
1 | a0002c0002t0002g0192 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.189-620_189-619ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747693 | |||||
| chr12:121747693
|
G | T | 22 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0255others(19): Show | 22 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.189-633G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747693 | ||||||
| chr12:121747693
|
G | TCTGGGGT others(989): Show |
1 | a0002c0002t0077g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.189-633delGinsTCTG others(993): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747693 | ||||||
| chr12:121747694
|
CTGGGGTA others(11): Show |
C | 7 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-631_189-614del others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747694 | ||||||
| chr12:121747695
|
T | A | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189-631T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747695 | ||||||
| chr12:121747699
|
G | A | 1 | a0002c0002t0088g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.189-627G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747699 | ||||||
| chr12:121747707
|
C | CGGGAGGC others(35): Show |
1 | a0002c0002t0003g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.189-600_189-599ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747707 | |||||
| chr12:121747707
|
C | T | 41 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.189-619C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747707 | ||||||
| chr12:121747707
|
C | TGGGAGGC others(137): Show |
2 | a0002c0002t0003g0087a0002c0002t0018g0086 | 2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.189-620_189-619ins others(144): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747707 | ||||||
| chr12:121747712
|
G | GTCTGGGG others(97): Show |
1 | a0001c0001t0083g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189-614_189-613ins others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747712 | ||||||
| chr12:121747713
|
G | A | 8 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(5): Show | 8 | HG00544.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-613G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747713 | ||||||
| chr12:121747713
|
G | GCA | 22 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0129others(19): Show | 22 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.189-612_189-611ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | GCACTGGG others(97): Show |
3 | a0002c0002t0037g0208a0002c0002t0039g0302a0002c0002t0098g0190 | 3 | HG01109.hp1 HG01496.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.189-612_189-611ins others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | GCACTGGG others(445): Show |
1 | a0002c0002t0008g0221 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.189-612_189-611ins others(452): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | GCTGGGGT others(15): Show |
2 | a0001c0001t0002g0022a0001c0001t0003g0107 | 2 | HG01943.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.189-592_189-591ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | GCTGGGGT others(15): Show |
1 | a0001c0001t0011g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.189-600_189-599ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | GCTGGGGT others(35): Show |
1 | a0002c0002t0001g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.189-600_189-599ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | GCTGGGGT others(427): Show |
1 | a0001c0001t0005g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189-600_189-599ins others(434): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747713 | |||||
| chr12:121747713
|
G | T | 34 | a0001c0001t0015g0096a0001c0001t0015g0116a0001c0001t0016g0061others(31): Show | 34 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.189-613G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747713 | ||||||
| chr12:121747713
|
G | TCTGGGGT others(559): Show |
1 | a0002c0002t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.189-614_189-613ins others(566): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747713 | ||||||
| chr12:121747713
|
G | TCTGGGGT others(621): Show |
1 | a0002c0002t0031g0091 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.189-613delGinsTCTG others(625): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747713 | ||||||
| chr12:121747713
|
G | TCTGGGGT others(521): Show |
1 | a0002c0002t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.189-614_189-613ins others(528): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747713 | ||||||
| chr12:121747713
|
G | TCTGGGGT others(521): Show |
1 | a0002c0002t0001g0249 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.189-614_189-613ins others(528): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747713 | ||||||
| chr12:121747727
|
C | CGGGAGGC others(983): Show |
1 | a0001c0001t0072g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.189-592_189-591ins others(990): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747727 | |||||
| chr12:121747727
|
C | CGGGAGGC others(859): Show |
1 | a0001c0001t0004g0203 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.189-592_189-591ins others(866): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747727 | |||||
| chr12:121747727
|
C | CGGGAGGC others(859): Show |
1 | a0001c0001t0004g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.189-592_189-591ins others(866): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747727 | |||||
| chr12:121747727
|
C | CGGGAGGC others(551): Show |
1 | a0001c0001t0011g0002 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.189-592_189-591ins others(558): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747727 | |||||
| chr12:121747727
|
C | CGGGAGGC others(735): Show |
1 | a0001c0001t0011g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.189-592_189-591ins others(742): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747727 | |||||
| chr12:121747727
|
C | T | 40 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0185others(37): Show | 41 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.189-599C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747727 | ||||||
| chr12:121747733
|
G | A | 1 | a0001c0001t0046g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.189-593G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747733 | ||||||
| chr12:121747733
|
G | GCA | 20 | a0001c0001t0001g0268a0001c0001t0002g0026a0001c0001t0006g0033others(17): Show | 20 | HG00280.hp1 HG00597.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-592_189-591ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747733 | |||||
| chr12:121747733
|
G | GCACTGGG others(81): Show |
1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-592_189-591ins others(88): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747733 | |||||
| chr12:121747733
|
G | GCTGGGGT others(323): Show |
1 | a0001c0001t0037g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189-572_189-571ins others(330): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747733 | |||||
| chr12:121747733
|
G | GCTGGGGT others(255): Show |
1 | a0001c0001t0003g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.189-514_189-513ins others(262): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747733 | |||||
| chr12:121747733
|
G | GCTGGGGT others(179): Show |
1 | a0001c0001t0101g0007 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.189-580_189-579ins others(186): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747733 | |||||
| chr12:121747733
|
G | T | 16 | a0001c0001t0016g0061a0001c0001t0043g0310a0001c0001t0044g0312others(13): Show | 16 | HG01071.hp2 HG01109.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.189-593G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747733 | ||||||
| chr12:121747733
|
G | TCTGGGGT others(499): Show |
1 | a0002c0002t0037g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.189-594_189-593ins others(506): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747733 | ||||||
| chr12:121747747
|
C | T | 44 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(41): Show | 45 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.189-579C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747747 | ||||||
| chr12:121747753
|
G | A | 4 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(1): Show | 4 | HG01109.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-573G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747753 | ||||||
| chr12:121747753
|
G | GCA | 25 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(22): Show | 25 | HG00280.hp2 HG01258.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-572_189-571ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | GCACTGGG others(35): Show |
1 | a0003c0003t0002g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.189-572_189-571ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | GCACTGGG others(37): Show |
1 | a0002c0002t0008g0293 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.189-572_189-571ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | GCTGGGGT others(33): Show |
1 | a0002c0002t0004g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.189-554_189-553ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | GCTGGGGT others(297): Show |
1 | a0002c0002t0065g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-554_189-553ins others(304): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | GCTGGGGT others(311): Show |
1 | a0001c0001t0082g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.189-560_189-559ins others(318): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | GCTGGGGT others(55): Show |
1 | a0002c0002t0007g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.189-560_189-559ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747753 | |||||
| chr12:121747753
|
G | T | 11 | a0001c0001t0043g0310a0001c0001t0044g0312a0002c0002t0001g0209others(8): Show | 11 | HG00280.hp1 HG00597.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-573G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747753 | ||||||
| chr12:121747754
|
CTGGGGTA others(91): Show |
C | 1 | a0001c0001t0079g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.189-571_189-474del others(98): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747754 | ||||||
| chr12:121747759
|
G | A | 2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-567G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747759 | ||||||
| chr12:121747759
|
G | GTAGAAGG others(57): Show |
1 | a0002c0002t0058g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.189-552_189-551ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747759 | |||||
| chr12:121747767
|
C | CGGGAGGC others(117): Show |
1 | a0001c0001t0011g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.189-552_189-551ins others(124): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747767 | |||||
| chr12:121747767
|
C | CGGGAGGC others(37): Show |
1 | a0001c0001t0010g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.189-552_189-551ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747767 | |||||
| chr12:121747767
|
C | CGGGAGGC others(551): Show |
2 | a0001c0001t0015g0096a0001c0001t0015g0116 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.189-552_189-551ins others(558): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747767 | |||||
| chr12:121747767
|
C | CGGGAGGC others(54): Show |
1 | a0001c0001t0069g0019 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.189-520_189-519ins others(61): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747767 | |||||
| chr12:121747767
|
C | CGGGAGTC others(631): Show |
1 | a0001c0001t0015g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.189-554_189-553ins others(638): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747767 | |||||
| chr12:121747767
|
C | T | 53 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0001g0185others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.189-559C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747767 | ||||||
| chr12:121747768
|
G | GGGAGGCT others(12): Show |
1 | a0001c0001t0033g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189-555_189-537dup others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747768 | |||||
| chr12:121747773
|
G | GCA | 19 | a0001c0001t0001g0045a0001c0001t0002g0020a0001c0001t0002g0023others(16): Show | 19 | HG00544.hp1 HG00558.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.189-552_189-551ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747773 | |||||
| chr12:121747773
|
G | GCACTGGG others(1831): Show |
1 | a0001c0001t0083g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189-552_189-551ins others(1838): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747773 | |||||
| chr12:121747773
|
G | GCACTGGG others(183): Show |
1 | a0001c0001t0054g0093 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.189-552_189-551ins others(190): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747773 | |||||
| chr12:121747773
|
G | GCTGGGGT others(35): Show |
1 | a0002c0002t0004g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.189-534_189-533ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747773 | |||||
| chr12:121747773
|
G | GCTGGGGT others(57): Show |
1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189-540_189-539ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747773 | |||||
| chr12:121747773
|
G | GCTGGGGT others(285): Show |
2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-540_189-539ins others(292): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747773 | |||||
| chr12:121747773
|
G | T | 22 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(19): Show | 22 | HG00597.hp1 HG01071.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.189-553G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747773 | ||||||
| chr12:121747787
|
C | CGGGAGGC others(123): Show |
1 | a0001c0001t0060g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.189-532_189-531ins others(130): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747787 | |||||
| chr12:121747787
|
C | T | 60 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.189-539C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747787 | ||||||
| chr12:121747787
|
C | TGGGAGGC others(3541): Show |
1 | a0001c0001t0011g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.189-540_189-539ins others(3548): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747787 | ||||||
| chr12:121747792
|
G | GTCTGGGG others(55): Show |
1 | a0002c0002t0031g0303 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.189-534_189-533ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747792 | ||||||
| chr12:121747792
|
G | GTCTGGGG others(157): Show |
1 | a0002c0002t0016g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-534_189-533ins others(164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747792 | ||||||
| chr12:121747793
|
G | A | 2 | a0002c0002t0016g0009a0002c0002t0031g0303 | 2 | HG02148.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.189-533G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747793 | ||||||
| chr12:121747793
|
G | GCA | 25 | a0001c0001t0001g0099a0001c0001t0001g0109a0001c0001t0001g0129others(22): Show | 25 | HG00280.hp2 HG00423.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.189-532_189-531ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747793 | |||||
| chr12:121747793
|
G | GCACTGGG others(55): Show |
3 | a0003c0003t0002g0284a0003c0003t0002g0285a0003c0003t0010g0068 | 3 | HG02615.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.189-532_189-531ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747793 | |||||
| chr12:121747793
|
G | GCACTGGG others(119): Show |
1 | a0002c0002t0096g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.189-532_189-531ins others(126): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747793 | |||||
| chr12:121747793
|
G | GCTGGGGT others(75): Show |
2 | a0003c0003t0002g0069a0003c0003t0010g0072 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.189-512_189-511ins others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747793 | |||||
| chr12:121747793
|
G | GCTGGGGT others(15): Show |
3 | a0002c0002t0001g0243a0002c0002t0004g0242a0002c0002t0010g0161 | 3 | HG00438.hp1 HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.189-520_189-519ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747793 | |||||
| chr12:121747793
|
G | T | 29 | a0001c0001t0001g0118a0001c0001t0001g0313a0001c0001t0002g0057others(26): Show | 29 | HG00544.hp1 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.189-533G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747793 | ||||||
| chr12:121747807
|
C | CGGGAGGC others(55): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-480_189-479ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747807 | |||||
| chr12:121747807
|
C | CGGGAGGC others(79): Show |
1 | a0001c0001t0057g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-500_189-499ins others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747807 | |||||
| chr12:121747807
|
C | T | 40 | a0001c0001t0001g0079a0001c0001t0001g0129a0001c0001t0001g0185others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.189-519C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747807 | ||||||
| chr12:121747812
|
G | GTCTGGGG others(697): Show |
1 | a0001c0001t0028g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.189-514_189-513ins others(704): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747812 | ||||||
| chr12:121747813
|
G | A | 1 | a0001c0001t0028g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.189-513G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747813 | ||||||
| chr12:121747813
|
G | GCA | 23 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0105others(20): Show | 23 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(20): Show |
intron_variant | MODIFIER | c.189-512_189-511ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCACTGGG others(3153): Show |
1 | a0001c0001t0001g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.189-512_189-511ins others(3160): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(35): Show |
1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189-472_189-471ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(77): Show |
1 | a0001c0001t0019g0034 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.189-438_189-437ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(1735): Show |
1 | a0001c0001t0005g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.189-480_189-479ins others(1742): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(1691): Show |
1 | a0001c0001t0005g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-480_189-479ins others(1698): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(35): Show |
1 | a0002c0002t0001g0201 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.189-494_189-493ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(199): Show |
1 | a0002c0002t0095g0245 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.189-494_189-493ins others(206): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | GCTGGGGT others(15): Show |
1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-500_189-499ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747813 | |||||
| chr12:121747813
|
G | T | 46 | a0001c0001t0002g0057a0001c0001t0003g0148a0001c0001t0003g0180others(43): Show | 46 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.189-513G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747813 | ||||||
| chr12:121747827
|
C | CGGGAGGC others(57): Show |
1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-492_189-491ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747827 | |||||
| chr12:121747827
|
C | CGGGAGGC others(15): Show |
2 | a0002c0002t0016g0009a0002c0002t0016g0286 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189-492_189-491ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747827 | |||||
| chr12:121747827
|
C | CGGGAGGC others(161): Show |
1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189-492_189-491ins others(168): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747827 | |||||
| chr12:121747827
|
C | T | 28 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0002g0026others(25): Show | 28 | HG00280.hp1 HG01109.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.189-499C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747827 | ||||||
| chr12:121747833
|
G | GCA | 18 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0002g0028others(15): Show | 18 | HG01257.hp1 HG01346.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.189-492_189-491ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | GCACTGGG others(215): Show |
1 | a0001c0001t0010g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.189-492_189-491ins others(222): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | GCTGGGGT others(15): Show |
2 | a0002c0002t0024g0197a0002c0002t0024g0207 | 2 | HG00735.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.189-472_189-471ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | GCTGGGGT others(437): Show |
1 | a0002c0002t0008g0223 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(444): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | GCTGGGGT others(55): Show |
1 | a0002c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | GCTGGGGT others(155): Show |
1 | a0001c0001t0011g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(162): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | GCTGGGGT others(13): Show |
1 | a0001c0009t0018g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189-474_189-473ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747833 | |||||
| chr12:121747833
|
G | T | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0171others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.189-493G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747833 | ||||||
| chr12:121747835
|
T | A | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189-491T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747835 | ||||||
| chr12:121747847
|
C | CGGGAGGC others(57): Show |
1 | a0002c0002t0004g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.189-472_189-471ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGGC others(545): Show |
2 | a0001c0001t0001g0185a0001c0001t0097g0311 | 2 | HG03927.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.189-468_189-467ins others(552): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGGC others(817): Show |
1 | a0002c0002t0088g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(824): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGGC others(323): Show |
2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.189-460_189-459ins others(330): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGGC others(95): Show |
1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGGC others(13): Show |
1 | a0002c0002t0004g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.189-471_189-452dup others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGGC others(99): Show |
1 | a0001c0001t0007g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.189-438_189-437ins others(106): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | CGGGAGTC others(55): Show |
1 | a0002c0002t0001g0170 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189-474_189-473ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747847 | |||||
| chr12:121747847
|
C | T | 56 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0026others(53): Show | 56 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.189-479C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747847 | ||||||
| chr12:121747853
|
G | A | 2 | a0001c0001t0005g0042a0001c0001t0079g0065 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189-473G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747853 | ||||||
| chr12:121747853
|
G | GCA | 30 | a0001c0001t0001g0099a0001c0001t0001g0313a0001c0001t0002g0022others(27): Show | 30 | HG00423.hp2 HG01099.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.189-472_189-471ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCACTGGG others(17): Show |
1 | a0001c0001t0006g0051 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.189-472_189-471ins others(24): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCACTGGG others(39): Show |
2 | a0001c0001t0002g0030a0001c0001t0002g0035 | 2 | HG03017.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.189-472_189-471ins others(46): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCACTGGG others(983): Show |
1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189-472_189-471ins others(990): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCACTGGG others(307): Show |
1 | a0001c0001t0012g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.189-472_189-471ins others(314): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(79): Show |
1 | a0001c0001t0062g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(1059): Show |
1 | a0001c0001t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(1066): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(293): Show |
2 | a0001c0001t0030g0159a0001c0001t0030g0162 | 2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.189-460_189-459ins others(300): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(273): Show |
2 | a0001c0001t0004g0217a0001c0001t0090g0294 | 2 | HG01123.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.189-460_189-459ins others(280): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(213): Show |
1 | a0001c0001t0017g0295 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(220): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(193): Show |
2 | a0001c0001t0023g0297a0001c0001t0023g0301 | 2 | HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.189-460_189-459ins others(200): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(153): Show |
1 | a0001c0001t0032g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(160): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(97): Show |
1 | a0001c0001t0002g0026 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(1163): Show |
1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(1170): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(53): Show |
4 | a0002c0002t0004g0218a0002c0002t0013g0037a0002c0002t0013g0039others(1): Show | 4 | HG00735.hp1 NA18955.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-460_189-459ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(77): Show |
2 | a0001c0001t0006g0050a0001c0001t0027g0273 | 2 | NA18973.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.189-460_189-459ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(99): Show |
1 | a0001c0001t0006g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(106): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(33): Show |
4 | a0002c0002t0001g0213a0002c0002t0007g0178a0002c0002t0007g0235others(1): Show | 4 | HG00642.hp2 HG02080.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-460_189-459ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(35): Show |
1 | a0001c0001t0002g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(57): Show |
1 | a0001c0001t0006g0049 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(13): Show |
21 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0002g0112others(18): Show | 21 | HG00741.hp2 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.189-460_189-459ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(35): Show |
1 | a0002c0002t0004g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.189-460_189-459ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(33): Show |
7 | a0001c0001t0011g0206a0001c0001t0103g0296a0002c0002t0012g0163others(4): Show | 7 | HG00323.hp2 HG02293.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-460_189-459ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(53): Show |
1 | a0001c0001t0032g0142 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.189-460_189-459ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | GCTGGGGT others(1397): Show |
1 | a0001c0001t0008g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(1404): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747853
|
G | T | 39 | a0001c0001t0005g0081a0001c0001t0005g0171a0001c0001t0008g0169others(36): Show | 39 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.189-473G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747853 | ||||||
| chr12:121747853
|
GCTGGGGT others(99): Show |
G | 3 | a0001c0001t0001g0129a0001c0001t0001g0277a0001c0001t0004g0041 | 3 | HG00280.hp2 HG03239.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.189-451_189-346del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747853 | |||||
| chr12:121747855
|
T | G | 1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-471T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747855 | ||||||
| chr12:121747867
|
T | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0002g0020others(122): Show | 125 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.189-459T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747867 | ||||||
| chr12:121747867
|
T | TGGGAGGC others(235): Show |
1 | a0002c0002t0007g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.189-438_189-437ins others(242): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747867 | |||||
| chr12:121747867
|
T | TGGGAGGC others(405): Show |
1 | a0001c0001t0028g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(412): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747867 | |||||
| chr12:121747867
|
T | TGGGAGGC others(175): Show |
1 | a0002c0002t0034g0001 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(182): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747867 | |||||
| chr12:121747872
|
GGC | G | 7 | a0001c0001t0003g0254a0001c0001t0042g0252a0001c0001t0109g0182others(4): Show | 7 | HG02895.hp1 HG03516.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-453_189-452del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747872 | ||||||
| chr12:121747873
|
G | T | 1 | a0001c0001t0111g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-453G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747873 | ||||||
| chr12:121747873
|
GCA | G | 55 | a0001c0001t0001g0006a0001c0001t0002g0057a0001c0001t0003g0003others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.189-451_189-450del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747873 | |||||
| chr12:121747874
|
C | CTGGGGTA others(11): Show |
1 | a0001c0001t0016g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(687): Show |
1 | a0001c0001t0025g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(694): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(273): Show |
1 | a0001c0001t0003g0253 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(280): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(313): Show |
2 | a0001c0001t0003g0256a0001c0001t0042g0250 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.189-452_189-451ins others(320): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(313): Show |
2 | a0001c0001t0003g0251a0001c0001t0003g0255 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.189-452_189-451ins others(320): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(71): Show |
2 | a0001c0001t0002g0136a0001c0001t0033g0135 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.189-452_189-451ins others(78): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(131): Show |
1 | a0001c0001t0002g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(138): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(31): Show |
1 | a0001c0001t0018g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(38): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(493): Show |
1 | a0001c0001t0111g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(500): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(299): Show |
1 | a0002c0002t0003g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(306): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(95): Show |
1 | a0001c0001t0025g0265 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(155): Show |
1 | a0002c0002t0003g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.189-452_189-451ins others(162): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747874
|
C | CTGGGGTA others(31): Show |
1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(38): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747874 | ||||||
| chr12:121747875
|
A | ACTGGGGT others(133): Show |
1 | a0003c0003t0061g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.189-438_189-437ins others(140): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747875 | |||||
| chr12:121747875
|
A | ACTGGGGT others(33): Show |
2 | a0002c0002t0007g0200a0002c0002t0105g0097 | 2 | HG02129.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.189-438_189-437ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747875 | |||||
| chr12:121747875
|
A | ACTGGGGT others(33): Show |
1 | a0002c0002t0098g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.189-438_189-437ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747875 | |||||
| chr12:121747875
|
A | G | 5 | a0001c0001t0003g0251a0001c0001t0025g0265a0001c0001t0111g0078others(2): Show | 5 | HG02004.hp2 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-451A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747875 | ||||||
| chr12:121747875
|
A | GCTGGGGT others(719): Show |
1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-452_189-451ins others(726): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747875 | ||||||
| chr12:121747875
|
A | T | 17 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0003g0253others(14): Show | 17 | HG02109.hp2 HG02135.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.189-451A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747875 | ||||||
| chr12:121747889
|
T | C | 138 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0092others(135): Show | 138 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.189-437T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747889 | ||||||
| chr12:121747889
|
T | TGGGAGGC others(601): Show |
1 | a0002c0002t0001g0199 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.189-430_189-429ins others(608): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747889 | |||||
| chr12:121747889
|
T | TGGGAGGC others(2003): Show |
1 | a0001c0001t0025g0265 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189-430_189-429ins others(2010): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747889 | |||||
| chr12:121747894
|
GGCTGGGG others(99): Show |
G | 1 | a0002c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.189-431_189-326del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747894 | ||||||
| chr12:121747895
|
G | A | 1 | a0001c0001t0026g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189-431G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747895 | ||||||
| chr12:121747895
|
G | GCA | 43 | a0001c0001t0001g0079a0001c0001t0001g0109a0001c0001t0001g0118others(40): Show | 43 | HG00621.hp1 HG01099.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.189-430_189-429ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCACTGGG others(17): Show |
4 | a0001c0001t0002g0023a0001c0001t0018g0024a0001c0001t0060g0167others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-430_189-429ins others(24): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCACTGGG others(121): Show |
1 | a0001c0001t0019g0053 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.189-430_189-429ins others(128): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCACTGGG others(1047): Show |
1 | a0002c0002t0014g0127 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.189-430_189-429ins others(1054): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCACTGGG others(1473): Show |
1 | a0002c0002t0004g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.189-430_189-429ins others(1480): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCACTGGG others(37): Show |
2 | a0001c0001t0019g0029a0001c0001t0019g0034 | 2 | NA18960.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.189-430_189-429ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCACTGGG others(307): Show |
1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.189-430_189-429ins others(314): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCTGGGGT others(141): Show |
1 | a0001c0001t0022g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.189-418_189-417ins others(148): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCTGGGGT others(157): Show |
1 | a0002c0002t0013g0038 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.189-418_189-417ins others(164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCTGGGGT others(233): Show |
1 | a0001c0001t0066g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.189-418_189-417ins others(240): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCTGGGGT others(1445): Show |
1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-418_189-417ins others(1452): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCTGGGGT others(102): Show |
1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-418_189-417ins others(109): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | GCTGGGGT others(1047): Show |
1 | a0001c0001t0049g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189-418_189-417ins others(1054): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
G | T | 16 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0004g0270others(13): Show | 16 | HG00423.hp1 HG01496.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.189-431G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747895 | ||||||
| chr12:121747895
|
GCTGGGGT others(15): Show |
G | 5 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0021g0013others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-409_189-388del others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747895
|
GCTGGGGT others(57): Show |
G | 2 | a0001c0001t0005g0149a0001c0001t0009g0289 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.189-409_189-346del others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747895 | |||||
| chr12:121747900
|
G | GGTAGAAG others(141): Show |
1 | a0001c0001t0002g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189-418_189-417ins others(148): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747900 | |||||
| chr12:121747900
|
G | GGTAGAAG others(473): Show |
1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.189-418_189-417ins others(480): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747900 | |||||
| chr12:121747909
|
T | C | 82 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0272others(79): Show | 82 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.189-417T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747909 | ||||||
| chr12:121747909
|
T | TGGGAGGC others(683): Show |
1 | a0002c0002t0017g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.189-404_189-403ins others(690): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747909 | |||||
| chr12:121747909
|
T | TGGGAGGC others(115): Show |
2 | a0002c0002t0024g0197a0002c0002t0024g0207 | 2 | HG00735.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.189-404_189-403ins others(122): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747909 | |||||
| chr12:121747909
|
T | TGGGAGGC others(177): Show |
2 | a0002c0002t0003g0087a0002c0002t0018g0086 | 2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.189-404_189-403ins others(184): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747909 | |||||
| chr12:121747909
|
T | TGGGAGGC others(579): Show |
1 | a0002c0002t0002g0192 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.189-410_189-409ins others(586): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747909 | |||||
| chr12:121747915
|
GCA | G | 57 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0026others(54): Show | 57 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.189-409_189-408del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747915 | |||||
| chr12:121747916
|
C | CTGGGGTA others(11): Show |
2 | a0001c0001t0040g0259a0001c0001t0040g0260 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.189-410_189-409ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747916 | ||||||
| chr12:121747916
|
C | CTGGGGTA others(1145): Show |
1 | a0002c0002t0096g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.189-410_189-409ins others(1152): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747916 | ||||||
| chr12:121747916
|
C | CTGGGGTA others(259): Show |
2 | a0001c0001t0001g0185a0001c0001t0097g0311 | 2 | HG03927.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.189-410_189-409ins others(266): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747916 | ||||||
| chr12:121747916
|
C | CTGGGGTA others(51): Show |
1 | a0002c0002t0045g0043 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.189-410_189-409ins others(58): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747916 | ||||||
| chr12:121747917
|
A | ACTGGGAT others(73): Show |
2 | a0002c0002t0022g0219a0002c0002t0031g0091 | 2 | HG01516.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.189-404_189-403ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(13): Show |
1 | a0003c0003t0010g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.189-396_189-395ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(667): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-396_189-395ins others(674): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(33): Show |
2 | a0001c0001t0004g0233a0001c0001t0011g0110 | 2 | HG01123.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.189-396_189-395ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(739): Show |
1 | a0002c0002t0014g0196 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.189-396_189-395ins others(746): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(13): Show |
1 | a0001c0001t0006g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.189-387_189-368dup others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(201): Show |
1 | a0001c0001t0054g0093 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.189-376_189-375ins others(208): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | ACTGGGGT others(75): Show |
1 | a0001c0001t0057g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-407_189-326dup others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747917 | |||||
| chr12:121747917
|
A | G | 6 | a0001c0001t0001g0185a0001c0001t0040g0259a0001c0001t0040g0260others(3): Show | 6 | HG00544.hp1 HG02258.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-409A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747917 | ||||||
| chr12:121747917
|
A | T | 1 | a0002c0002t0091g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.189-409A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747917 | ||||||
| chr12:121747923
|
G | A | 5 | a0002c0002t0001g0189a0002c0002t0003g0290a0002c0002t0017g0088others(2): Show | 5 | HG00597.hp2 HG01257.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-403G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747923 | ||||||
| chr12:121747931
|
T | C | 50 | a0001c0001t0001g0099a0001c0001t0004g0203a0001c0001t0005g0008others(47): Show | 50 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.189-395T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747931 | ||||||
| chr12:121747931
|
T | TGGGAGGC others(13): Show |
6 | a0003c0003t0002g0069a0003c0003t0002g0284a0003c0003t0002g0285others(3): Show | 6 | HG01884.hp2 HG02630.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-376_189-375ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747931 | |||||
| chr12:121747937
|
G | GCA | 28 | a0001c0001t0001g0092a0001c0001t0001g0272a0001c0001t0002g0026others(25): Show | 28 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.189-388_189-387ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(17): Show |
2 | a0001c0001t0004g0233a0001c0001t0011g0110 | 2 | HG01123.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.189-388_189-387ins others(24): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(37): Show |
1 | a0001c0001t0004g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.189-388_189-387ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(159): Show |
1 | a0001c0001t0056g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.189-388_189-387ins others(166): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(531): Show |
1 | a0001c0001t0005g0040 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.189-388_189-387ins others(538): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(257): Show |
1 | a0002c0002t0001g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.189-388_189-387ins others(264): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(631): Show |
1 | a0001c0001t0050g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189-388_189-387ins others(638): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCACTGGG others(753): Show |
1 | a0001c0001t0005g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.189-388_189-387ins others(760): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(1329): Show |
1 | a0001c0001t0001g0109 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.189-376_189-375ins others(1336): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(133): Show |
2 | a0001c0001t0040g0259a0001c0001t0040g0260 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.189-376_189-375ins others(140): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(529): Show |
1 | a0001c0001t0011g0102 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189-376_189-375ins others(536): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(93): Show |
1 | a0002c0002t0012g0174 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-376_189-375ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(569): Show |
1 | a0001c0001t0075g0181 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.189-376_189-375ins others(576): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(33): Show |
1 | a0002c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189-376_189-375ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(73): Show |
2 | a0002c0002t0001g0189a0002c0002t0003g0290 | 2 | HG02083.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189-376_189-375ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(57): Show |
4 | a0001c0001t0004g0203a0001c0001t0011g0002a0001c0001t0011g0119others(1): Show | 4 | HG01928.hp1 HG01934.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-376_189-375ins others(64): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(73): Show |
1 | a0002c0002t0031g0303 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.189-376_189-375ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(1757): Show |
1 | a0001c0001t0025g0264 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.189-354_189-353ins others(1764): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(303): Show |
1 | a0001c0001t0083g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189-368_189-367ins others(310): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | GCTGGGGT others(267): Show |
1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-368_189-367ins others(274): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747937
|
G | T | 7 | a0001c0001t0025g0271a0002c0002t0007g0186a0002c0002t0009g0058others(4): Show | 7 | HG01071.hp2 HG01516.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-389G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747937 | ||||||
| chr12:121747937
|
GCTGGGGT others(15): Show |
G | 1 | a0001c0001t0020g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.189-367_189-346del others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747937 | |||||
| chr12:121747942
|
G | GGTAGAAG others(35): Show |
1 | a0001c0001t0005g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.189-368_189-367ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747942 | |||||
| chr12:121747942
|
G | GGTAGAAG others(408): Show |
1 | a0001c0001t0005g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189-368_189-367ins others(415): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747942 | |||||
| chr12:121747951
|
T | C | 36 | a0001c0001t0002g0112a0001c0001t0081g0108a0001c0001t0082g0073others(33): Show | 36 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.189-375T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747951 | ||||||
| chr12:121747951
|
T | TGGGAGGC others(157): Show |
3 | a0002c0002t0007g0166a0002c0002t0007g0178a0002c0002t0085g0205 | 3 | HG00438.hp2 HG02080.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.189-362_189-361ins others(164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747951 | |||||
| chr12:121747951
|
T | TGGGAGGC others(115): Show |
3 | a0002c0002t0003g0278a0002c0002t0004g0224a0002c0002t0015g0306 | 3 | HG02055.hp2 HG04199.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.189-362_189-361ins others(122): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747951 | |||||
| chr12:121747951
|
T | TGGGAGGC others(157): Show |
1 | a0002c0002t0024g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189-362_189-361ins others(164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747951 | |||||
| chr12:121747951
|
T | TGGGAGGC others(601): Show |
1 | a0002c0002t0039g0111 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.189-354_189-353ins others(608): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747951 | |||||
| chr12:121747951
|
T | TGGGAGGC others(703): Show |
1 | a0002c0002t0039g0302 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.189-368_189-367ins others(710): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747951 | |||||
| chr12:121747953
|
G | A | 1 | a0001c0001t0026g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189-373G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747953 | ||||||
| chr12:121747957
|
GCA | G | 37 | a0001c0001t0001g0099a0001c0001t0001g0268a0001c0001t0002g0026others(34): Show | 37 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.189-367_189-366del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747957 | |||||
| chr12:121747958
|
C | CTGGGGTA others(117): Show |
1 | a0002c0002t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.189-368_189-367ins others(124): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747958
|
C | CTGGGGTA others(353): Show |
1 | a0002c0002t0004g0242 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.189-368_189-367ins others(360): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747958
|
C | CTGGGGTA others(31): Show |
1 | a0002c0002t0017g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.189-368_189-367ins others(38): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747958
|
C | CTGGGGTA others(11): Show |
1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-368_189-367ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747958
|
C | CTGGGGTA others(53): Show |
1 | a0002c0002t0004g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189-368_189-367ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747958
|
C | CTGGGGTA others(33): Show |
4 | a0001c0001t0001g0272a0001c0001t0005g0025a0001c0001t0027g0066others(1): Show | 4 | HG00621.hp1 HG03491.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-368_189-367ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747958
|
C | CTGGGGTA others(301): Show |
1 | a0001c0001t0001g0313 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189-368_189-367ins others(308): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747958 | ||||||
| chr12:121747959
|
A | ACTGGGAT others(73): Show |
7 | a0002c0002t0012g0080a0002c0002t0012g0163a0002c0002t0012g0175others(4): Show | 7 | HG01258.hp1 HG01943.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-362_189-361ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747959 | |||||
| chr12:121747959
|
A | ACTGGGGT others(13): Show |
1 | a0002c0002t0003g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.189-354_189-353ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747959 | |||||
| chr12:121747959
|
A | ACTGGGGT others(845): Show |
1 | a0002c0002t0095g0245 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.189-354_189-353ins others(852): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747959 | |||||
| chr12:121747959
|
A | ACTGGGGT others(299): Show |
1 | a0002c0002t0034g0001 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.189-354_189-353ins others(306): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747959 | |||||
| chr12:121747959
|
A | ACTGGGGT others(723): Show |
1 | a0002c0002t0007g0200 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.189-354_189-353ins others(730): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747959 | |||||
| chr12:121747959
|
A | ACTGGGGT others(13): Show |
6 | a0001c0001t0002g0020a0001c0001t0010g0052a0001c0001t0019g0029others(3): Show | 6 | HG02056.hp1 HG03834.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-345_189-326dup others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747959 | |||||
| chr12:121747959
|
A | G | 8 | a0001c0001t0001g0272a0001c0001t0001g0313a0001c0001t0002g0112others(5): Show | 8 | HG00621.hp1 HG02074.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-367A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747959 | ||||||
| chr12:121747959
|
A | T | 4 | a0002c0002t0004g0242a0002c0002t0009g0058a0002c0002t0017g0088others(1): Show | 4 | HG00673.hp1 HG01257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-367A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747959 | ||||||
| chr12:121747961
|
T | A | 12 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-365T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747961 | ||||||
| chr12:121747965
|
G | A | 32 | a0001c0001t0008g0115a0002c0002t0001g0184a0002c0002t0001g0194others(29): Show | 32 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.189-361G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747965 | ||||||
| chr12:121747973
|
T | C | 54 | a0001c0001t0001g0129a0001c0001t0001g0277a0001c0001t0002g0057others(51): Show | 55 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.189-353T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747973 | ||||||
| chr12:121747979
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0002g0035 | 2 | HG03017.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.189-347G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747979 | ||||||
| chr12:121747979
|
G | GCA | 6 | a0001c0001t0002g0028a0001c0001t0002g0030a0001c0001t0002g0112others(3): Show | 6 | HG02074.hp1 NA18942.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-346_189-345ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCACTGGG others(1779): Show |
1 | a0001c0001t0011g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189-346_189-345ins others(1786): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCACTGGG others(37): Show |
1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189-346_189-345ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(639): Show |
1 | a0002c0002t0096g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.189-334_189-333ins others(646): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(355): Show |
1 | a0002c0002t0001g0243 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.189-334_189-333ins others(362): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(651): Show |
1 | a0002c0002t0008g0309 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.189-334_189-333ins others(658): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(355): Show |
1 | a0002c0002t0001g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.189-334_189-333ins others(362): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(375): Show |
1 | a0002c0002t0089g0244 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.189-334_189-333ins others(382): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(599): Show |
1 | a0002c0002t0004g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.189-334_189-333ins others(606): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(53): Show |
1 | a0002c0002t0017g0279 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.189-334_189-333ins others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(73): Show |
23 | a0002c0002t0001g0184a0002c0002t0001g0199a0002c0002t0001g0201others(20): Show | 23 | HG00323.hp1 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.189-334_189-333ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(175): Show |
1 | a0002c0002t0001g0194 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.189-334_189-333ins others(182): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(195): Show |
1 | a0002c0002t0001g0213 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.189-334_189-333ins others(202): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(93): Show |
1 | a0002c0002t0022g0304 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.189-334_189-333ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(435): Show |
1 | a0002c0002t0010g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.189-334_189-333ins others(442): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | GCTGGGGT others(15): Show |
1 | a0001c0001t0002g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189-325_189-304dup others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747979 | |||||
| chr12:121747979
|
G | T | 23 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(20): Show | 24 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.189-347G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747979 | ||||||
| chr12:121747983
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0002g0035 | 2 | HG03017.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.189-343G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747983 | ||||||
| chr12:121747984
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0002g0035 | 2 | HG03017.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.189-342G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747984 | ||||||
| chr12:121747984
|
G | GGTAGAAG others(15): Show |
1 | a0001c0001t0002g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.189-328_189-327ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747984 | |||||
| chr12:121747984
|
G | GGTAGAAG others(1473): Show |
1 | a0001c0001t0081g0108 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.189-326_189-325ins others(1480): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747984 | |||||
| chr12:121747984
|
G | GGTAGAAG others(97): Show |
1 | a0001c0001t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.189-326_189-325ins others(104): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747984 | |||||
| chr12:121747993
|
T | C | 84 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0003g0107others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.189-333T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747993 | ||||||
| chr12:121747993
|
T | TGGGAGGC others(115): Show |
2 | a0002c0002t0086g0291a0002c0002t0104g0165 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189-320_189-319ins others(122): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(115): Show |
1 | a0002c0002t0004g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.189-320_189-319ins others(122): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(15): Show |
1 | a0002c0002t0013g0038 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.189-312_189-311ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(417): Show |
1 | a0002c0002t0105g0097 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.189-312_189-311ins others(424): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(597): Show |
1 | a0002c0002t0098g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.189-312_189-311ins others(604): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(1049): Show |
1 | a0002c0002t0008g0293 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.189-312_189-311ins others(1056): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(601): Show |
2 | a0002c0002t0008g0221a0002c0002t0008g0292 | 2 | HG02155.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.189-326_189-325ins others(608): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(497): Show |
1 | a0002c0002t0045g0043 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.189-326_189-325ins others(504): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(457): Show |
1 | a0002c0002t0004g0103 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.189-326_189-325ins others(464): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747993
|
T | TGGGAGGC others(701): Show |
1 | a0002c0002t0007g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.189-326_189-325ins others(708): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747993 | |||||
| chr12:121747994
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-332G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747994 | ||||||
| chr12:121747998
|
G | A | 1 | a0001c0001t0026g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189-328G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747998 | ||||||
| chr12:121747998
|
GGC | G | 5 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-327_189-326del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121747998 | ||||||
| chr12:121747999
|
GCA | G | 32 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0129others(29): Show | 32 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.189-325_189-324del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121747999 | |||||
| chr12:121748000
|
C | CTGGGGTA others(11): Show |
1 | a0002c0002t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.189-326_189-325ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748000 | ||||||
| chr12:121748000
|
C | CTGGGGTA others(71): Show |
1 | a0001c0001t0004g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.189-326_189-325ins others(78): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748000 | ||||||
| chr12:121748000
|
C | CTGGGGTA others(629): Show |
1 | a0001c0001t0008g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.189-326_189-325ins others(636): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748000 | ||||||
| chr12:121748000
|
C | CTGGGGTA others(31): Show |
3 | a0002c0002t0014g0227a0002c0002t0014g0228a0002c0002t0077g0257 | 3 | HG01433.hp2 HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.189-326_189-325ins others(38): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748000 | ||||||
| chr12:121748000
|
C | CTGGGGTA others(33): Show |
1 | a0001c0001t0002g0022 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.189-326_189-325ins others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748000 | ||||||
| chr12:121748000
|
C | CTGGGGTA others(519): Show |
1 | a0001c0001t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.189-326_189-325ins others(526): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748000 | ||||||
| chr12:121748001
|
A | ACTGGGAT others(73): Show |
1 | a0002c0002t0002g0192 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.189-320_189-319ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748001 | |||||
| chr12:121748001
|
A | ACTGGGGT others(73): Show |
2 | a0001c0001t0017g0295a0001c0001t0030g0159 | 2 | HG01934.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.189-312_189-311ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748001 | |||||
| chr12:121748001
|
A | ACTGGGGT others(93): Show |
3 | a0001c0001t0005g0171a0001c0001t0023g0297a0001c0001t0023g0301 | 3 | HG02602.hp2 HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.189-312_189-311ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748001 | |||||
| chr12:121748001
|
A | ACTGGGGT others(113): Show |
1 | a0001c0001t0023g0298 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.189-312_189-311ins others(120): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748001 | |||||
| chr12:121748001
|
A | ACTGGGGT others(2049): Show |
1 | a0002c0002t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-312_189-311ins others(2056): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748001 | |||||
| chr12:121748001
|
A | ACTGGGGT others(73): Show |
1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748001 | |||||
| chr12:121748001
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0002g0022a0001c0001t0004g0217others(1): Show | 4 | HG00423.hp2 HG01952.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-325A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748001 | ||||||
| chr12:121748001
|
A | T | 10 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(7): Show | 10 | HG00280.hp1 HG01106.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-325A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748001 | ||||||
| chr12:121748003
|
T | A | 9 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0016g0308others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-323T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748003 | ||||||
| chr12:121748007
|
G | A | 7 | a0002c0002t0004g0128a0002c0002t0004g0204a0002c0002t0007g0166others(4): Show | 7 | HG00438.hp2 HG01255.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-319G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748007 | ||||||
| chr12:121748015
|
T | C | 103 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0001g0176others(100): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.189-311T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748015 | ||||||
| chr12:121748015
|
T | TGGGAGGC others(93): Show |
1 | a0001c0001t0030g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.189-292_189-291ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748015 | |||||
| chr12:121748015
|
T | TGGGAGGC others(237): Show |
1 | a0001c0001t0056g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(244): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748015 | |||||
| chr12:121748020
|
G | GAC | 12 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0059others(9): Show | 12 | HG02129.hp1 HG02698.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-306_189-305ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748020 | ||||||
| chr12:121748021
|
G | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0059others(9): Show | 12 | HG02129.hp1 HG02698.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-305G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748021 | ||||||
| chr12:121748021
|
G | GCA | 15 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0028others(12): Show | 15 | HG01099.hp1 HG01891.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.189-304_189-303ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCACTGGG others(35): Show |
1 | a0001c0001t0005g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.189-304_189-303ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCACTGGG others(35): Show |
1 | a0001c0001t0006g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.189-304_189-303ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCTGGGGT others(73): Show |
3 | a0002c0002t0004g0128a0002c0002t0014g0127a0002c0002t0014g0198 | 3 | HG01255.hp1 NA18942.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.189-292_189-291ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCTGGGGT others(15): Show |
1 | a0001c0001t0006g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.189-283_189-262dup others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCTGGGGT others(1053): Show |
1 | a0001c0001t0106g0048 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.189-220_189-219ins others(1060): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCTGGGGT others(197): Show |
1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(204): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | GCTGGGGT others(343): Show |
1 | a0001c0001t0004g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(350): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748021 | |||||
| chr12:121748021
|
G | T | 7 | a0002c0002t0001g0177a0002c0002t0001g0195a0002c0002t0002g0192others(4): Show | 7 | HG00558.hp2 HG00597.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-305G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748021 | ||||||
| chr12:121748025
|
G | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0059others(9): Show | 12 | HG02129.hp1 HG02698.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-301G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748025 | ||||||
| chr12:121748026
|
G | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0005g0059others(9): Show | 12 | HG02129.hp1 HG02698.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-300G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748026 | ||||||
| chr12:121748026
|
G | GGTAGAAG others(285): Show |
1 | a0001c0001t0001g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.189-292_189-291ins others(292): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(887): Show |
1 | a0001c0001t0028g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-292_189-291ins others(894): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(839): Show |
1 | a0001c0001t0012g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.189-292_189-291ins others(846): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(35): Show |
19 | a0001c0001t0001g0104a0001c0001t0001g0313a0001c0001t0004g0203others(16): Show | 19 | HG00544.hp2 HG01123.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.189-284_189-283ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(245): Show |
1 | a0001c0001t0022g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(252): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(265): Show |
1 | a0001c0001t0037g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(272): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(95): Show |
1 | a0001c0001t0001g0109 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(102): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(427): Show |
1 | a0001c0001t0015g0269 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(434): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748026
|
G | GGTAGAAG others(407): Show |
1 | a0001c0001t0041g0261 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(414): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748026 | |||||
| chr12:121748035
|
T | C | 85 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0004g0276others(82): Show | 86 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.189-291T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748035 | ||||||
| chr12:121748035
|
T | TGGGAGGC others(115): Show |
4 | a0002c0002t0001g0193a0002c0002t0007g0166a0002c0002t0007g0178others(1): Show | 4 | HG00438.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-278_189-277ins others(122): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748035 | |||||
| chr12:121748035
|
T | TGGGAGGC others(157): Show |
1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189-270_189-269ins others(164): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748035 | |||||
| chr12:121748035
|
T | TGGGAGGC others(241): Show |
2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.189-270_189-269ins others(248): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748035 | |||||
| chr12:121748035
|
T | TGGGAGGC others(93): Show |
1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748035 | |||||
| chr12:121748035
|
T | TGGGAGGC others(1701): Show |
1 | a0002c0002t0001g0170 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(1708): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748035 | |||||
| chr12:121748036
|
G | A | 1 | a0002c0002t0088g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.189-290G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748036 | ||||||
| chr12:121748037
|
G | A | 12 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-289G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748037 | ||||||
| chr12:121748041
|
G | A | 2 | a0001c0001t0008g0115a0001c0001t0011g0119 | 2 | HG01934.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.189-285G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748041 | ||||||
| chr12:121748041
|
GCA | G | 28 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0277others(25): Show | 28 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.189-283_189-282del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748041 | |||||
| chr12:121748042
|
C | CTGGGGTA others(51): Show |
1 | a0001c0001t0008g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(58): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(71): Show |
2 | a0001c0001t0074g0299a0001c0001t0090g0294 | 2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.189-284_189-283ins others(78): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(91): Show |
1 | a0001c0001t0107g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(98): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(337): Show |
1 | a0001c0001t0101g0007 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(344): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(91): Show |
8 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0004g0276others(5): Show | 8 | HG00323.hp2 HG02683.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-284_189-283ins others(98): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(111): Show |
1 | a0002c0002t0088g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(118): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(11): Show |
1 | a0001c0001t0030g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189-284_189-283ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(55): Show |
2 | a0001c0001t0025g0264a0001c0001t0025g0265 | 2 | HG02004.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.189-284_189-283ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(55): Show |
2 | a0001c0001t0005g0113a0001c0001t0057g0018 | 2 | HG02280.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.189-284_189-283ins others(62): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(553): Show |
1 | a0001c0001t0025g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(560): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748042
|
C | CTGGGGTA others(427): Show |
1 | a0001c0001t0041g0262 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.189-284_189-283ins others(434): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748042 | ||||||
| chr12:121748043
|
A | ACTGAAGT others(35): Show |
2 | a0001c0001t0008g0115a0001c0001t0011g0119 | 2 | HG01934.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.189-280_189-279ins others(42): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | ACTGGGGT others(13): Show |
1 | a0002c0002t0014g0228 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.189-270_189-269ins others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | ACTGGGGT others(637): Show |
1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-270_189-269ins others(644): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | ACTGGGGT others(13): Show |
1 | a0001c0001t0005g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.189-261_189-242dup others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | ACTGGGGT others(423): Show |
1 | a0001c0001t0003g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.189-250_189-249ins others(430): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | ACTGGGGT others(237): Show |
1 | a0001c0001t0059g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.189-180_189-179ins others(244): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | ACTGGGGT others(237): Show |
1 | a0001c0001t0011g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.189-180_189-179ins others(244): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748043
|
A | G | 21 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0004g0276others(18): Show | 21 | HG00323.hp2 HG00621.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.189-283A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748043 | ||||||
| chr12:121748043
|
ACTGGGGT others(13): Show |
A | 2 | a0001c0001t0081g0108a0002c0002t0065g0275 | 2 | HG01517.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.189-261_189-242del others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748043 | |||||
| chr12:121748045
|
T | A | 3 | a0001c0001t0005g0149a0001c0001t0009g0289a0001c0001t0109g0182 | 3 | HG02965.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.189-281T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748045 | ||||||
| chr12:121748049
|
G | A | 1 | a0002c0002t0014g0196 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.189-277G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748049 | ||||||
| chr12:121748057
|
T | C | 20 | a0001c0001t0001g0099a0001c0001t0002g0112a0001c0001t0056g0047others(17): Show | 20 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-269T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748057 | ||||||
| chr12:121748063
|
G | GCA | 18 | a0001c0001t0001g0268a0001c0001t0002g0022a0001c0001t0002g0028others(15): Show | 18 | HG00423.hp1 HG01517.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.189-262_189-261ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748063 | |||||
| chr12:121748063
|
G | GCACTGGG others(2693): Show |
1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-262_189-261ins others(2700): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748063 | |||||
| chr12:121748063
|
G | GCTGGGGT others(73): Show |
1 | a0002c0002t0014g0196 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.189-250_189-249ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748063 | |||||
| chr12:121748063
|
G | GCTGGGGT others(15): Show |
49 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0109others(46): Show | 49 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.189-241_189-220dup others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748063 | |||||
| chr12:121748063
|
G | GCTGGGGT others(199): Show |
1 | a0001c0001t0007g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.189-242_189-241ins others(206): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748063 | |||||
| chr12:121748063
|
G | GCTGGGGT others(99): Show |
1 | a0001c0001t0011g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189-242_189-241ins others(106): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748063 | |||||
| chr12:121748063
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-263G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748063 | ||||||
| chr12:121748077
|
T | C | 11 | a0001c0001t0001g0099a0001c0001t0082g0073a0002c0002t0001g0193others(8): Show | 11 | HG00423.hp2 HG01071.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-249T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748077 | ||||||
| chr12:121748077
|
T | TGGGAGGC others(197): Show |
1 | a0002c0002t0004g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.189-242_189-241ins others(204): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748077 | |||||
| chr12:121748078
|
G | A | 1 | a0002c0002t0008g0223 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.189-248G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748078 | ||||||
| chr12:121748079
|
G | A | 13 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0009g0004others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.189-247G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748079 | ||||||
| chr12:121748082
|
G | A | 7 | a0001c0001t0005g0008a0001c0001t0009g0151a0001c0001t0009g0152others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-244G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748082 | ||||||
| chr12:121748083
|
GCA | G | 19 | a0001c0001t0001g0099a0001c0001t0001g0185a0001c0001t0005g0008others(16): Show | 19 | HG00423.hp2 HG00738.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.189-241_189-240del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748083 | |||||
| chr12:121748084
|
C | CTGGGGTA others(73): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-242_189-241ins others(80): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748084 | ||||||
| chr12:121748085
|
A | ACTGGGGT others(175): Show |
1 | a0001c0001t0082g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.189-220_189-219ins others(182): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748085 | |||||
| chr12:121748085
|
A | ACTGGGGT others(75): Show |
1 | a0001c0001t0010g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.189-182_189-181ins others(82): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748085 | |||||
| chr12:121748085
|
A | GCTGGGGT others(15): Show |
1 | a0004c0005t0004g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189-263_189-242dup others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748085 | ||||||
| chr12:121748085
|
ACTGGGGT others(13): Show |
A | 12 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0020g0125others(9): Show | 12 | HG00558.hp1 HG01167.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-179_189-160del others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748085 | |||||
| chr12:121748085
|
ACTGGGGT others(33): Show |
A | 1 | a0001c0001t0046g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.189-199_189-160del others(40): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748085 | |||||
| chr12:121748099
|
T | C | 8 | a0001c0001t0001g0185a0001c0001t0002g0112a0001c0001t0043g0310others(5): Show | 8 | HG00280.hp1 HG01071.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-227T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748099 | ||||||
| chr12:121748101
|
G | A | 1 | a0001c0001t0021g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189-225G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748101 | ||||||
| chr12:121748105
|
G | GCA | 12 | a0001c0001t0001g0104a0001c0001t0004g0233a0001c0001t0006g0050others(9): Show | 12 | HG00738.hp1 HG01123.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-220_189-219ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748105 | |||||
| chr12:121748105
|
G | GCTGGGGT others(15): Show |
11 | a0001c0001t0003g0003a0001c0001t0003g0251a0001c0001t0003g0253others(8): Show | 11 | HG02071.hp1 HG02109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-200_189-199ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748105 | |||||
| chr12:121748105
|
G | T | 6 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(3): Show | 6 | HG00280.hp1 HG02723.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-221G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748105 | ||||||
| chr12:121748106
|
CTGGGGTA others(93): Show |
C | 7 | a0001c0001t0005g0008a0001c0001t0009g0151a0001c0001t0009g0152others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-219_189-120del others(100): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748106 | ||||||
| chr12:121748119
|
T | C | 2 | a0001c0001t0001g0176a0002c0002t0001g0209 | 2 | HG00280.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.189-207T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748119 | ||||||
| chr12:121748120
|
G | A | 5 | a0002c0002t0003g0084a0002c0002t0003g0085a0002c0002t0003g0087others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-206G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748120 | ||||||
| chr12:121748121
|
G | A | 3 | a0001c0001t0005g0149a0001c0001t0009g0289a0001c0001t0109g0182 | 3 | HG02965.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.189-205G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748121 | ||||||
| chr12:121748124
|
G | A | 12 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0009g0004others(9): Show | 12 | HG01109.hp2 HG01169.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-202G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748124 | ||||||
| chr12:121748125
|
G | GCA | 218 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.189-200_189-199ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCACTGGG others(59): Show |
1 | a0001c0001t0006g0055 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.189-200_189-199ins others(66): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCACTGGG others(165): Show |
1 | a0002c0002t0008g0223 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.189-200_189-199ins others(172): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCACTGGG others(37): Show |
2 | a0001c0001t0001g0099a0001c0001t0007g0266 | 2 | HG00423.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.189-200_189-199ins others(44): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCTGGGGT others(679): Show |
1 | a0001c0001t0008g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189-187_189-186ins others(686): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCTGGGGT others(143): Show |
1 | a0001c0001t0004g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.189-182_189-181ins others(150): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCTGGGGT others(143): Show |
1 | a0001c0001t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.189-182_189-181ins others(150): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCTGGGGT others(77): Show |
4 | a0001c0001t0002g0023a0001c0001t0018g0024a0001c0001t0060g0167others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-182_189-181ins others(84): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCTGGGGT others(15): Show |
9 | a0001c0001t0001g0104a0001c0001t0004g0233a0001c0001t0006g0050others(6): Show | 9 | HG01123.hp2 HG01433.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.189-180_189-179ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | GCTGGGGT others(341): Show |
1 | a0001c0001t0082g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.189-168_189-167ins others(348): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748125 | |||||
| chr12:121748125
|
G | T | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189-201G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748125 | ||||||
| chr12:121748139
|
T | C | 6 | a0001c0001t0001g0176a0001c0001t0017g0295a0001c0001t0023g0297others(3): Show | 6 | HG00280.hp1 HG00323.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-187T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748139 | ||||||
| chr12:121748144
|
G | A | 2 | a0001c0001t0020g0125a0001c0001t0021g0013 | 2 | HG01167.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.189-182G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748144 | ||||||
| chr12:121748145
|
G | GCA | 9 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-180_189-179ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748145 | |||||
| chr12:121748145
|
G | GCACTGGG others(79): Show |
1 | a0001c0001t0002g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189-180_189-179ins others(86): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748145 | |||||
| chr12:121748145
|
G | T | 5 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-181G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748145 | ||||||
| chr12:121748146
|
CTGGGGTA others(53): Show |
C | 6 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0020g0122others(3): Show | 6 | HG01169.hp1 HG01255.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-179_189-120del others(60): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748146 | ||||||
| chr12:121748159
|
T | C | 2 | a0001c0001t0002g0112a0002c0002t0004g0210 | 2 | HG02074.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.189-167T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748159 | ||||||
| chr12:121748160
|
G | A | 4 | a0002c0002t0001g0305a0002c0002t0031g0091a0002c0002t0031g0303others(1): Show | 4 | HG01496.hp2 HG01928.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-166G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748160 | ||||||
| chr12:121748164
|
G | A | 3 | a0001c0001t0005g0149a0001c0001t0009g0289a0001c0001t0109g0182 | 3 | HG02965.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.189-162G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748164 | ||||||
| chr12:121748164
|
GGC | G | 5 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-161_189-160del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748164 | ||||||
| chr12:121748165
|
GCA | G | 12 | a0001c0001t0005g0149a0001c0001t0009g0289a0001c0001t0109g0182others(9): Show | 12 | HG00280.hp1 HG00735.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-159_189-158del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748165 | |||||
| chr12:121748166
|
C | CTGGGGTA others(11): Show |
1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-160_189-159ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748166 | ||||||
| chr12:121748166
|
C | CTGGGGTA others(441): Show |
1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189-160_189-159ins others(448): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748166 | ||||||
| chr12:121748167
|
A | ACTGGGGT others(13): Show |
1 | a0002c0002t0031g0303 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.189-124_189-105dup others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748167 | |||||
| chr12:121748167
|
A | G | 3 | a0001c0001t0102g0083a0002c0002t0001g0189a0005c0006t0047g0144 | 3 | HG02083.hp2 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.189-159A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748167 | ||||||
| chr12:121748167
|
A | T | 5 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-159A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748167 | ||||||
| chr12:121748167
|
ACTGGGGT others(13): Show |
A | 10 | a0001c0001t0021g0013a0002c0002t0003g0290a0002c0002t0004g0090others(7): Show | 10 | HG01258.hp2 HG01358.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-124_189-105del others(20): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748167 | |||||
| chr12:121748181
|
T | C | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189-145T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748181 | ||||||
| chr12:121748182
|
GGGAGGCT others(33): Show |
G | 1 | a0001c0001t0020g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.189-137_189-98delT others(39): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748182 | |||||
| chr12:121748186
|
G | GAC | 7 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-140_189-139ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748186 | ||||||
| chr12:121748187
|
G | A | 7 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-139G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748187 | ||||||
| chr12:121748187
|
G | GCA | 23 | a0001c0001t0002g0112a0001c0001t0005g0042a0001c0001t0056g0047others(20): Show | 23 | HG00280.hp1 HG00423.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.189-138_189-137ins others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748187 | |||||
| chr12:121748187
|
G | GCTGGGGT others(611): Show |
1 | a0002c0002t0004g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189-126_189-125ins others(618): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748187 | |||||
| chr12:121748187
|
G | GCTGGGGT others(15): Show |
77 | a0002c0002t0001g0170a0002c0002t0001g0177a0002c0002t0001g0184others(74): Show | 78 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.189-118_189-117ins others(22): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748187 | |||||
| chr12:121748187
|
G | GCTGGGGT others(245): Show |
2 | a0002c0002t0016g0009a0002c0002t0016g0286 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189-118_189-117ins others(252): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748187 | |||||
| chr12:121748188
|
CTGGGGTA others(11): Show |
C | 3 | a0001c0001t0005g0149a0001c0001t0009g0289a0001c0001t0109g0182 | 3 | HG02965.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.189-137_189-120del others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748188 | ||||||
| chr12:121748191
|
G | A | 7 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-135G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748191 | ||||||
| chr12:121748192
|
G | A | 7 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-134G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748192 | ||||||
| chr12:121748201
|
T | TGGGAGGC others(217): Show |
1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.189-118_189-117ins others(224): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748201 | |||||
| chr12:121748201
|
T | TGGGAGGC others(217): Show |
3 | a0001c0001t0043g0310a0001c0001t0044g0312a0001c0001t0097g0311 | 3 | NA19054.hp1 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189-118_189-117ins others(224): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748201 | |||||
| chr12:121748202
|
GGGAGGCT others(13): Show |
G | 1 | a0001c0001t0021g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189-117_189-98delT others(19): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748202 | |||||
| chr12:121748207
|
G | A | 16 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(13): Show | 16 | HG01169.hp1 HG01255.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.189-119G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748207 | ||||||
| chr12:121748222
|
A | G | 24 | a0001c0001t0001g0185a0001c0001t0002g0112a0001c0001t0005g0008others(21): Show | 24 | HG00423.hp1 HG01169.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.189-104A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748222 | ||||||
| chr12:121748229
|
A | ACTGGGGT others(1495): Show |
1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-84_189-83insCG others(1500): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 121748229 | |||||
| chr12:121748243
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-83T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 2/11 | chr12 | 121748243 | ||||||
| chr12:121748456
|
A | G | 3 | a0001c0001t0016g0061a0001c0001t0021g0288a0001c0001t0076g0287 | 3 | HG01243.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.305+14A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748456 | ||||||
| chr12:121748554
|
G | T | 1 | a0001c0001t0055g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.305+112G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748554 | ||||||
| chr12:121748558
|
A | G | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.305+116A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748558 | ||||||
| chr12:121748694
|
A | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.305+252A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748694 | ||||||
| chr12:121748725
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.305+283C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748725 | ||||||
| chr12:121748762
|
G | T | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.305+320G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748762 | ||||||
| chr12:121748813
|
A | T | 1 | a0002c0002t0015g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.305+371A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121748813 | ||||||
| chr12:121749093
|
C | G | 16 | a0002c0002t0001g0194a0002c0002t0001g0199a0002c0002t0001g0209others(13): Show | 17 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.305+651C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749093 | ||||||
| chr12:121749175
|
A | G | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.305+733A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749175 | ||||||
| chr12:121749221
|
A | G | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.305+779A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749221 | ||||||
| chr12:121749479
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.306-901C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749479 | ||||||
| chr12:121749499
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.306-881T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749499 | ||||||
| chr12:121749553
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.306-827C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749553 | ||||||
| chr12:121749597
|
G | A | 1 | a0001c0001t0023g0298 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.306-783G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749597 | ||||||
| chr12:121749624
|
C | T | 6 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.306-756C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749624 | ||||||
| chr12:121749789
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.306-591C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749789 | ||||||
| chr12:121749850
|
G | A | 1 | a0001c0001t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.306-530G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749850 | ||||||
| chr12:121749893
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.306-487G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749893 | ||||||
| chr12:121749905
|
C | CA | 11 | a0001c0001t0003g0300a0001c0001t0006g0051a0001c0001t0008g0169others(8): Show | 11 | HG00621.hp2 HG01934.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.306-460dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 121749905 | |||||
| chr12:121749905
|
CA | C | 31 | a0001c0001t0002g0136a0001c0001t0003g0148a0001c0001t0003g0180others(28): Show | 31 | HG00323.hp1 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.306-460delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 121749905 | |||||
| chr12:121749918
|
A | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.306-462A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121749918 | ||||||
| chr12:121750059
|
T | C | 13 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.306-321T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121750059 | ||||||
| chr12:121750126
|
G | A | 7 | a0002c0002t0012g0080a0002c0002t0012g0163a0002c0002t0012g0174others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.306-254G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 3/11 | chr12 | 121750126 | ||||||
| chr12:121750484
|
CCCCACA | C | 10 | a0001c0001t0001g0268a0001c0001t0011g0263a0001c0001t0025g0264others(7): Show | 10 | HG01978.hp1 HG02004.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+61_365+66delAC others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750484 | |||||
| chr12:121750564
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.365+125T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750564 | ||||||
| chr12:121750582
|
T | G | 2 | a0001c0001t0054g0093a0001c0001t0057g0018 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.365+143T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750582 | ||||||
| chr12:121750601
|
CACACCA | C | 108 | a0002c0002t0001g0170a0002c0002t0001g0177a0002c0002t0001g0184others(105): Show | 109 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.365+181_365+186del others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750601 | |||||
| chr12:121750644
|
C | T | 108 | a0002c0002t0001g0170a0002c0002t0001g0177a0002c0002t0001g0184others(105): Show | 109 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.365+205C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750644 | ||||||
| chr12:121750646
|
AACCCAC | A | 6 | a0001c0001t0005g0042a0001c0001t0005g0081a0001c0001t0079g0065others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+230_365+235del others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750646 | |||||
| chr12:121750817
|
CCCACACC others(4): Show |
C | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+385_365+395del others(11): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750817 | |||||
| chr12:121750829
|
C | A | 1 | a0002c0002t0001g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.365+390C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750829 | ||||||
| chr12:121750835
|
A | G | 1 | a0001c0001t0004g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.365+396A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750835 | ||||||
| chr12:121750849
|
C | T | 2 | a0001c0001t0021g0288a0001c0001t0076g0287 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.365+410C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750849 | ||||||
| chr12:121750880
|
A | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+441A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750880 | ||||||
| chr12:121750889
|
C | T | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+450C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750889 | ||||||
| chr12:121750897
|
A | G | 1 | a0001c0001t0059g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.365+458A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750897 | ||||||
| chr12:121750899
|
ACCCACAC | A | 7 | a0001c0001t0016g0061a0001c0001t0017g0295a0001c0001t0023g0297others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.365+477_365+483del others(7): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750899 | |||||
| chr12:121750903
|
A | T | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+464A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750903 | ||||||
| chr12:121750921
|
C | T | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+482C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750921 | ||||||
| chr12:121750922
|
C | A | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+483C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750922 | ||||||
| chr12:121750928
|
T | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+489T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750928 | ||||||
| chr12:121750932
|
C | A | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+493C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750932 | ||||||
| chr12:121750939
|
C | A | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+500C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750939 | ||||||
| chr12:121750966
|
A | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+527A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121750966 | ||||||
| chr12:121750977
|
A | ACCCACAC | 217 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(214): Show | 218 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.365+557_365+563dup others(7): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750977 | |||||
| chr12:121750977
|
A | ACCCACAC others(7): Show |
19 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.365+550_365+563dup others(14): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750977 | |||||
| chr12:121750977
|
ACCCACAC | A | 3 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0033g0135 | 3 | HG02896.hp1 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.365+557_365+563del others(7): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 121750977 | |||||
| chr12:121751332
|
A | C | 1 | a0001c0001t0005g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.366-796A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121751332 | ||||||
| chr12:121751486
|
T | G | 5 | a0002c0002t0009g0058a0002c0002t0016g0009a0002c0002t0016g0286others(2): Show | 5 | HG02451.hp2 HG03139.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-642T>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121751486 | ||||||
| chr12:121751614
|
G | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.366-514G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121751614 | ||||||
| chr12:121751697
|
G | A | 6 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-431G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121751697 | ||||||
| chr12:121751745
|
G | A | 1 | a0002c0002t0003g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-383G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121751745 | ||||||
| chr12:121751947
|
C | G | 13 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.366-181C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121751947 | ||||||
| chr12:121752012
|
CCTT | C | 18 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.366-115_366-113del others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 4/11 | chr12 | 121752012 | ||||||
| chr12:121752314
|
C | T | 1 | a0001c0001t0067g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.461+91C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752314 | ||||||
| chr12:121752469
|
A | G | 1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.461+246A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752469 | ||||||
| chr12:121752473
|
C | T | 1 | a0002c0002t0003g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.461+250C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752473 | ||||||
| chr12:121752479
|
G | A | 98 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(95): Show | 98 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.461+256G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752479 | ||||||
| chr12:121752614
|
ATGGTGGA others(108): Show |
A | 1 | a0002c0002t0008g0223 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.461+392_461+506del | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752614 | ||||||
| chr12:121752633
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.461+410G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752633 | ||||||
| chr12:121752645
|
C | T | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.461+422C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752645 | ||||||
| chr12:121752708
|
G | A | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.461+485G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752708 | ||||||
| chr12:121752750
|
C | CA | 7 | a0001c0001t0001g0185a0001c0001t0011g0263a0001c0001t0043g0310others(4): Show | 7 | HG01978.hp1 HG02738.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+535dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121752750 | |||||
| chr12:121752769
|
G | C | 3 | a0002c0002t0008g0221a0002c0002t0008g0292a0002c0002t0008g0293 | 3 | HG02155.hp1 NA19054.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.461+546G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752769 | ||||||
| chr12:121752884
|
G | A | 1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.461+661G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752884 | ||||||
| chr12:121752992
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.461+769C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121752992 | ||||||
| chr12:121753021
|
C | T | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.461+798C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753021 | ||||||
| chr12:121753114
|
AGG | A | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.461+893_461+894del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121753114 | |||||
| chr12:121753120
|
A | G | 1 | a0001c0001t0019g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.461+897A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753120 | ||||||
| chr12:121753141
|
C | T | 1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.461+918C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753141 | ||||||
| chr12:121753320
|
G | T | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.461+1097G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753320 | ||||||
| chr12:121753347
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.461+1124T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753347 | ||||||
| chr12:121753359
|
A | G | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.461+1136A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753359 | ||||||
| chr12:121753580
|
CA | C | 31 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.461+1368delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121753580 | |||||
| chr12:121753584
|
A | C | 119 | a0001c0001t0002g0026a0001c0001t0005g0042a0001c0001t0012g0074others(116): Show | 120 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.461+1361A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753584 | ||||||
| chr12:121753585
|
A | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.461+1362A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753585 | ||||||
| chr12:121753644
|
A | G | 1 | a0001c0001t0011g0280 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.461+1421A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753644 | ||||||
| chr12:121753706
|
TA | T | 27 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(24): Show | 27 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.461+1494delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121753706 | |||||
| chr12:121753819
|
C | T | 1 | a0001c0001t0006g0055 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.461+1596C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753819 | ||||||
| chr12:121753940
|
A | G | 30 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.461+1717A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121753940 | ||||||
| chr12:121754235
|
ACTC | A | 5 | a0002c0002t0014g0196a0002c0002t0014g0198a0002c0002t0014g0227others(2): Show | 5 | HG01071.hp2 HG01255.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+2016_461+2018d others(5): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121754235 | |||||
| chr12:121754485
|
G | A | 2 | a0001c0004t0099g0010a0001c0004t0100g0082 | 2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.461+2262G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121754485 | ||||||
| chr12:121754625
|
C | A | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.461+2402C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121754625 | ||||||
| chr12:121754660
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.461+2437G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121754660 | ||||||
| chr12:121754714
|
T | C | 1 | a0002c0002t0088g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.461+2491T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121754714 | ||||||
| chr12:121755070
|
G | A | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.461+2847G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121755070 | ||||||
| chr12:121755524
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0003g0247a0001c0001t0003g0248others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+3301C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121755524 | ||||||
| chr12:121755533
|
T | C | 1 | a0001c0001t0071g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.461+3310T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121755533 | ||||||
| chr12:121755660
|
T | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.461+3437T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121755660 | ||||||
| chr12:121755858
|
A | T | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.461+3635A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121755858 | ||||||
| chr12:121755987
|
G | A | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.461+3764G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121755987 | ||||||
| chr12:121756039
|
A | G | 1 | a0001c0001t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.461+3816A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756039 | ||||||
| chr12:121756041
|
A | G | 65 | a0001c0001t0001g0185a0001c0001t0001g0272a0001c0001t0002g0020others(62): Show | 65 | HG00621.hp1 HG01099.hp1 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.461+3818A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756041 | ||||||
| chr12:121756219
|
C | T | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.461+3996C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756219 | ||||||
| chr12:121756605
|
A | T | 1 | a0001c0001t0005g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.461+4382A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756605 | ||||||
| chr12:121756821
|
A | C | 1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.461+4598A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756821 | ||||||
| chr12:121756826
|
C | T | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.461+4603C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756826 | ||||||
| chr12:121756944
|
C | T | 3 | a0001c0001t0029g0076a0001c0001t0029g0077a0002c0002t0001g0195 | 3 | HG01106.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.462-4705C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756944 | ||||||
| chr12:121756984
|
G | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-4665G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121756984 | ||||||
| chr12:121757140
|
T | TG | 53 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0268others(50): Show | 53 | HG00423.hp1 HG00544.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.462-4497dupG | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121757140 | |||||
| chr12:121757140
|
TG | T | 135 | a0001c0001t0001g0079a0001c0001t0004g0203a0001c0001t0005g0008others(132): Show | 136 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.462-4497delG | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121757140 | |||||
| chr12:121757141
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.462-4508G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757141 | ||||||
| chr12:121757145
|
G | T | 1 | a0002c0002t0002g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.462-4504G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757145 | ||||||
| chr12:121757146
|
G | T | 108 | a0001c0001t0004g0203a0002c0002t0001g0170a0002c0002t0001g0177others(105): Show | 109 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.462-4503G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757146 | ||||||
| chr12:121757168
|
A | G | 8 | a0001c0001t0003g0003a0001c0001t0003g0251a0001c0001t0003g0253others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.462-4481A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757168 | ||||||
| chr12:121757220
|
G | A | 1 | a0001c0001t0005g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.462-4429G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757220 | ||||||
| chr12:121757308
|
C | T | 1 | a0002c0002t0004g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.462-4341C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757308 | ||||||
| chr12:121757384
|
G | A | 131 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0179others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.462-4265G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757384 | ||||||
| chr12:121757395
|
G | A | 1 | a0001c0001t0005g0008 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.462-4254G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757395 | ||||||
| chr12:121757428
|
G | A | 1 | a0001c0001t0004g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.462-4221G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757428 | ||||||
| chr12:121757520
|
A | AT | 82 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0099others(79): Show | 82 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.462-4126dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121757520 | |||||
| chr12:121757520
|
A | ATT | 3 | a0001c0001t0005g0081a0001c0001t0015g0101a0001c0001t0055g0095 | 3 | HG02698.hp2 HG02738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.462-4127_462-4126d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121757520 | |||||
| chr12:121757520
|
A | T | 1 | a0001c0001t0008g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.462-4129A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757520 | ||||||
| chr12:121757522
|
T | TA | 13 | a0001c0001t0001g0045a0001c0001t0001g0118a0001c0001t0002g0112others(10): Show | 13 | HG00423.hp1 HG02074.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.462-4127_462-4126i others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757522 | ||||||
| chr12:121757523
|
T | A | 34 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(31): Show | 34 | HG00673.hp1 HG01109.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.462-4126T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757523 | ||||||
| chr12:121757524
|
A | T | 312 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0079others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.462-4125A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757524 | ||||||
| chr12:121757525
|
T | A | 3 | a0001c0001t0015g0269a0001c0001t0041g0261a0001c0001t0041g0262 | 3 | NA19004.hp1 NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.462-4124T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757525 | ||||||
| chr12:121757526
|
T | A | 11 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0016g0308others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.462-4123T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757526 | ||||||
| chr12:121757617
|
T | C | 31 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.462-4032T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757617 | ||||||
| chr12:121757773
|
C | G | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3876C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757773 | ||||||
| chr12:121757901
|
C | T | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.462-3748C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121757901 | ||||||
| chr12:121758091
|
C | T | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-3558C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758091 | ||||||
| chr12:121758127
|
G | A | 30 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.462-3522G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758127 | ||||||
| chr12:121758157
|
T | C | 3 | a0001c0001t0015g0269a0001c0001t0041g0261a0001c0001t0041g0262 | 3 | NA19004.hp1 NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.462-3492T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758157 | ||||||
| chr12:121758199
|
C | T | 1 | a0001c0001t0018g0024 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.462-3450C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758199 | ||||||
| chr12:121758206
|
A | G | 31 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.462-3443A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758206 | ||||||
| chr12:121758226
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0069g0019 | 2 | NA18747.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.462-3423G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758226 | ||||||
| chr12:121758315
|
C | T | 1 | a0001c0001t0111g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.462-3334C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758315 | ||||||
| chr12:121758382
|
G | A | 15 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.462-3267G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758382 | ||||||
| chr12:121758395
|
G | A | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-3254G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758395 | ||||||
| chr12:121758402
|
TCACCATG others(67): Show |
T | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.462-3144_462-3071d others(76): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121758402 | |||||
| chr12:121758432
|
G | A | 1 | a0002c0002t0068g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.462-3217G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758432 | ||||||
| chr12:121758492
|
C | T | 1 | a0002c0002t0007g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.462-3157C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758492 | ||||||
| chr12:121758503
|
C | T | 1 | a0001c0001t0079g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.462-3146C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758503 | ||||||
| chr12:121758505
|
C | T | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.462-3144C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758505 | ||||||
| chr12:121758513
|
TCACCATG others(30): Show |
T | 22 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(19): Show | 22 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-3120_462-3084d others(39): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121758513 | |||||
| chr12:121758529
|
T | C | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3120T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758529 | ||||||
| chr12:121758534
|
T | C | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3115T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758534 | ||||||
| chr12:121758538
|
T | C | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3111T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758538 | ||||||
| chr12:121758541
|
A | G | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3108A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758541 | ||||||
| chr12:121758550
|
C | T | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3099C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758550 | ||||||
| chr12:121758578
|
G | A | 9 | a0001c0001t0002g0057a0003c0003t0002g0069a0003c0003t0002g0274others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.462-3071G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758578 | ||||||
| chr12:121758579
|
T | C | 25 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.462-3070T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758579 | ||||||
| chr12:121758604
|
G | A | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-3045G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758604 | ||||||
| chr12:121758608
|
C | T | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3041C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758608 | ||||||
| chr12:121758612
|
C | T | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3037C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758612 | ||||||
| chr12:121758614
|
C | T | 1 | a0001c0001t0107g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.462-3035C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758614 | ||||||
| chr12:121758615
|
G | A | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-3034G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758615 | ||||||
| chr12:121758616
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.462-3033C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758616 | ||||||
| chr12:121758624
|
T | C | 1 | a0001c0001t0030g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.462-3025T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758624 | ||||||
| chr12:121758640
|
C | T | 22 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(19): Show | 22 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-3009C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758640 | ||||||
| chr12:121758645
|
C | T | 22 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(19): Show | 22 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-3004C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758645 | ||||||
| chr12:121758649
|
C | T | 22 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(19): Show | 22 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-3000C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758649 | ||||||
| chr12:121758652
|
G | A | 23 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(20): Show | 23 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.462-2997G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758652 | ||||||
| chr12:121758677
|
T | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-2972T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758677 | ||||||
| chr12:121758682
|
T | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0004g0203others(23): Show | 26 | HG01109.hp2 HG01496.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-2967T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758682 | ||||||
| chr12:121758682
|
T | TAGCTCCA others(30): Show |
3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.462-2926_462-2890d others(39): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121758682 | |||||
| chr12:121758691
|
G | A | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.462-2958G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758691 | ||||||
| chr12:121758751
|
C | T | 6 | a0001c0001t0017g0295a0001c0001t0023g0297a0001c0001t0023g0298others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.462-2898C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758751 | ||||||
| chr12:121758825
|
C | T | 1 | a0001c0001t0079g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.462-2824C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758825 | ||||||
| chr12:121758840
|
T | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-2809T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758840 | ||||||
| chr12:121758911
|
G | A | 6 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0026g0015others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.462-2738G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121758911 | ||||||
| chr12:121759122
|
G | GT | 140 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0179others(137): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.462-2513dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121759122 | |||||
| chr12:121759122
|
G | GTT | 81 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(78): Show | 81 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.462-2514_462-2513d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121759122 | |||||
| chr12:121759122
|
G | GTTT | 43 | a0001c0001t0001g0109a0001c0001t0001g0272a0001c0001t0001g0313others(40): Show | 43 | HG00621.hp1 HG01099.hp1 HG01516.hp2 others(40): Show |
intron_variant | MODIFIER | c.462-2515_462-2513d others(5): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121759122 | |||||
| chr12:121759178
|
G | T | 3 | a0001c0004t0003g0012a0001c0004t0099g0010a0001c0004t0100g0082 | 3 | HG02809.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.462-2471G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759178 | ||||||
| chr12:121759236
|
C | T | 1 | a0001c0001t0016g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.462-2413C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759236 | ||||||
| chr12:121759238
|
C | CGTTAGT | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-2409_462-2404d others(8): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121759238 | |||||
| chr12:121759400
|
G | T | 14 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.462-2249G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759400 | ||||||
| chr12:121759410
|
G | T | 14 | a0001c0001t0005g0149a0001c0001t0009g0004a0001c0001t0009g0005others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.462-2239G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759410 | ||||||
| chr12:121759425
|
C | G | 1 | a0001c0001t0006g0267 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.462-2224C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759425 | ||||||
| chr12:121759430
|
C | T | 1 | a0001c0001t0020g0122 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.462-2219C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759430 | ||||||
| chr12:121759551
|
G | A | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-2098G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759551 | ||||||
| chr12:121759691
|
G | A | 1 | a0002c0002t0008g0309 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.462-1958G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759691 | ||||||
| chr12:121759780
|
T | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-1869T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759780 | ||||||
| chr12:121759935
|
A | G | 1 | a0001c0001t0011g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.462-1714A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759935 | ||||||
| chr12:121759995
|
A | G | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-1654A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121759995 | ||||||
| chr12:121760079
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.462-1570C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760079 | ||||||
| chr12:121760129
|
C | CA | 43 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0001g0109others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.462-1496dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121760129 | |||||
| chr12:121760129
|
CA | C | 24 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0004g0041others(21): Show | 24 | HG00280.hp2 HG00544.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.462-1496delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121760129 | |||||
| chr12:121760227
|
C | T | 95 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(92): Show | 95 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.462-1422C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760227 | ||||||
| chr12:121760267
|
C | T | 19 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.462-1382C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760267 | ||||||
| chr12:121760269
|
C | T | 19 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.462-1380C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760269 | ||||||
| chr12:121760294
|
CA | C | 27 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(24): Show | 27 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.462-1344delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121760294 | |||||
| chr12:121760340
|
G | A | 1 | a0001c0001t0092g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.462-1309G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760340 | ||||||
| chr12:121760378
|
CCTGGGGT | C | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-1268_462-1262d others(9): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 121760378 | |||||
| chr12:121760415
|
G | A | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-1234G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760415 | ||||||
| chr12:121760486
|
C | T | 1 | a0001c0001t0016g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.462-1163C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760486 | ||||||
| chr12:121760574
|
T | A | 3 | a0001c0001t0015g0096a0001c0001t0015g0101a0001c0001t0015g0116 | 3 | HG02698.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.462-1075T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760574 | ||||||
| chr12:121760603
|
T | C | 5 | a0001c0001t0005g0042a0001c0001t0079g0065a0001c0004t0003g0012others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-1046T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760603 | ||||||
| chr12:121760611
|
G | A | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-1038G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760611 | ||||||
| chr12:121760870
|
A | G | 1 | a0002c0002t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.462-779A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121760870 | ||||||
| chr12:121761181
|
A | C | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.462-468A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121761181 | ||||||
| chr12:121761231
|
A | G | 30 | a0001c0001t0001g0185a0001c0001t0003g0148a0001c0001t0003g0180others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.462-418A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121761231 | ||||||
| chr12:121761339
|
G | A | 4 | a0002c0002t0013g0036a0002c0002t0013g0037a0002c0002t0013g0038others(1): Show | 4 | NA18955.hp1 NA18956.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.462-310G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121761339 | ||||||
| chr12:121761418
|
G | A | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-231G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121761418 | ||||||
| chr12:121761507
|
C | T | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.462-142C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121761507 | ||||||
| chr12:121761538
|
G | A | 35 | a0001c0001t0001g0272a0001c0001t0002g0020a0001c0001t0002g0021others(32): Show | 35 | HG00621.hp1 HG01099.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.462-111G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 5/11 | chr12 | 121761538 | ||||||
| chr12:121761749
|
A | G | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.551+11A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121761749 | ||||||
| chr12:121761868
|
C | G | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.551+130C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121761868 | ||||||
| chr12:121761902
|
T | C | 1 | a0002c0002t0002g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.551+164T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121761902 | ||||||
| chr12:121761964
|
T | C | 1 | a0002c0002t0002g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.551+226T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121761964 | ||||||
| chr12:121762013
|
C | T | 1 | a0001c0001t0010g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.551+275C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762013 | ||||||
| chr12:121762108
|
T | C | 1 | a0002c0002t0010g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.551+370T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762108 | ||||||
| chr12:121762220
|
C | T | 1 | a0001c0001t0071g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.551+482C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762220 | ||||||
| chr12:121762271
|
C | CA | 33 | a0001c0001t0001g0185a0001c0001t0002g0030a0001c0001t0003g0148others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.551+549dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121762271 | |||||
| chr12:121762271
|
CA | C | 8 | a0001c0001t0002g0136a0001c0001t0028g0240a0001c0001t0028g0241others(5): Show | 8 | HG01517.hp1 HG02129.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.551+549delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121762271 | |||||
| chr12:121762476
|
C | T | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.551+738C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762476 | ||||||
| chr12:121762513
|
C | G | 97 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(94): Show | 97 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.551+775C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762513 | ||||||
| chr12:121762679
|
C | T | 2 | a0001c0001t0008g0044a0001c0001t0106g0048 | 2 | HG02074.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.551+941C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762679 | ||||||
| chr12:121762806
|
G | A | 1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.551+1068G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121762806 | ||||||
| chr12:121763149
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.551+1411C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763149 | ||||||
| chr12:121763157
|
C | CT | 17 | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0001t0001g0268others(14): Show | 17 | HG01346.hp1 HG02071.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.551+1442dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121763157 | |||||
| chr12:121763157
|
CT | C | 115 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0004g0203others(112): Show | 116 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.551+1442delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121763157 | |||||
| chr12:121763159
|
T | C | 5 | a0002c0002t0003g0084a0002c0002t0003g0085a0002c0002t0003g0087others(2): Show | 5 | HG02055.hp2 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.551+1421T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763159 | ||||||
| chr12:121763181
|
G | A | 2 | a0001c0001t0066g0138a0001c0001t0067g0046 | 2 | HG02071.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.551+1443G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763181 | ||||||
| chr12:121763236
|
C | G | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.551+1498C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763236 | ||||||
| chr12:121763248
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0007g0266 | 2 | NA18940.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.551+1510C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763248 | ||||||
| chr12:121763255
|
C | T | 1 | a0001c0001t0071g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.551+1517C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763255 | ||||||
| chr12:121763256
|
G | A | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.551+1518G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763256 | ||||||
| chr12:121763351
|
A | G | 15 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.551+1613A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763351 | ||||||
| chr12:121763383
|
C | T | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.551+1645C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763383 | ||||||
| chr12:121763454
|
A | G | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.551+1716A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763454 | ||||||
| chr12:121763467
|
G | A | 3 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126 | 3 | HG01167.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.551+1729G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763467 | ||||||
| chr12:121763495
|
G | T | 1 | a0002c0002t0004g0090 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.551+1757G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763495 | ||||||
| chr12:121763545
|
C | T | 2 | a0001c0001t0003g0148a0001c0001t0003g0180 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.551+1807C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763545 | ||||||
| chr12:121763991
|
G | A | 8 | a0003c0003t0002g0069a0003c0003t0002g0274a0003c0003t0002g0284others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.551+2253G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121763991 | ||||||
| chr12:121764029
|
C | T | 2 | a0001c0001t0005g0042a0001c0001t0079g0065 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.551+2291C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764029 | ||||||
| chr12:121764099
|
G | A | 2 | a0001c0001t0021g0288a0001c0001t0076g0287 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.551+2361G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764099 | ||||||
| chr12:121764159
|
C | CA | 18 | a0001c0001t0003g0180a0001c0001t0005g0008a0001c0001t0005g0149others(15): Show | 18 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.551+2421_551+2422i others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764159 | ||||||
| chr12:121764159
|
C | CAA | 4 | a0001c0001t0003g0148a0001c0001t0035g0133a0001c0001t0109g0182others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.551+2421_551+2422i others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764159 | ||||||
| chr12:121764160
|
C | A | 26 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.551+2422C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764160 | ||||||
| chr12:121764160
|
C | CA | 24 | a0001c0001t0001g0129a0001c0001t0002g0057a0001c0001t0005g0060others(21): Show | 24 | HG01433.hp1 HG01891.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.551+2440dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121764160 | |||||
| chr12:121764250
|
G | A | 2 | a0002c0002t0024g0197a0002c0002t0024g0211 | 2 | HG00735.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.551+2512G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764250 | ||||||
| chr12:121764294
|
G | GA | 24 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.551+2556_551+2557i others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764294 | ||||||
| chr12:121764295
|
T | C | 24 | a0001c0001t0005g0008a0001c0001t0005g0149a0001c0001t0009g0004others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.551+2557T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764295 | ||||||
| chr12:121764526
|
A | C | 1 | a0001c0001t0005g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.551+2788A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764526 | ||||||
| chr12:121764617
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.551+2879C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764617 | ||||||
| chr12:121764653
|
C | CA | 6 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(3): Show | 6 | HG03927.hp1 NA18955.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.551+2927dupA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121764653 | |||||
| chr12:121764715
|
A | T | 4 | a0001c0001t0049g0158a0001c0001t0050g0155a0001c0001t0051g0154others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.551+2977A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121764715 | ||||||
| chr12:121765004
|
C | CCATTCAT others(4): Show |
1 | a0003c0003t0010g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551+3271_551+3281d others(13): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121765004 | |||||
| chr12:121765121
|
T | TTTTC | 24 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0005g0008others(21): Show | 24 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.551+3391_551+3394d others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121765121 | |||||
| chr12:121765129
|
C | CT | 18 | a0001c0001t0001g0006a0001c0001t0002g0023a0001c0001t0003g0247others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.551+3409dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121765129 | |||||
| chr12:121765129
|
CT | C | 10 | a0001c0001t0001g0185a0001c0001t0002g0147a0001c0001t0003g0107others(7): Show | 10 | HG01516.hp1 HG01943.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.551+3409delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121765129 | |||||
| chr12:121765389
|
T | C | 38 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0003g0148others(35): Show | 38 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.551+3651T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121765389 | ||||||
| chr12:121765774
|
C | T | 106 | a0001c0001t0003g0148a0001c0001t0004g0203a0001c0001t0005g0042others(103): Show | 107 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.551+4036C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121765774 | ||||||
| chr12:121765981
|
C | T | 1 | a0002c0002t0094g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.551+4243C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121765981 | ||||||
| chr12:121765983
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.551+4245C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121765983 | ||||||
| chr12:121766009
|
C | T | 242 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0092others(239): Show | 243 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.551+4271C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766009 | ||||||
| chr12:121766159
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.551+4421C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766159 | ||||||
| chr12:121766178
|
C | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0104others(84): Show | 87 | HG00544.hp2 HG00621.hp1 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.551+4440C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766178 | ||||||
| chr12:121766284
|
A | C | 21 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0003g0148others(18): Show | 21 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.551+4546A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766284 | ||||||
| chr12:121766307
|
G | GCTT | 26 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0001g0185others(23): Show | 26 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.551+4571_551+4572i others(5): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121766307 | |||||
| chr12:121766347
|
G | T | 1 | a0002c0002t0053g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.552-4560G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766347 | ||||||
| chr12:121766429
|
A | G | 4 | a0001c0001t0049g0158a0001c0001t0050g0155a0001c0001t0051g0154others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.552-4478A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766429 | ||||||
| chr12:121766502
|
C | T | 1 | a0001c0001t0092g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.552-4405C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766502 | ||||||
| chr12:121766555
|
C | T | 2 | a0001c0001t0022g0098a0001c0001t0037g0094 | 2 | HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.552-4352C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766555 | ||||||
| chr12:121766581
|
G | C | 1 | a0001c0001t0102g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.552-4326G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766581 | ||||||
| chr12:121766620
|
G | A | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.552-4287G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766620 | ||||||
| chr12:121766807
|
T | A | 3 | a0002c0002t0008g0221a0002c0002t0008g0292a0002c0002t0008g0293 | 3 | HG02155.hp1 NA19054.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.552-4100T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766807 | ||||||
| chr12:121766835
|
C | T | 1 | a0002c0002t0002g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.552-4072C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766835 | ||||||
| chr12:121766964
|
T | C | 23 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0003g0148others(20): Show | 23 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.552-3943T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121766964 | ||||||
| chr12:121767047
|
C | T | 88 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0105others(85): Show | 88 | HG00544.hp2 HG00621.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.552-3860C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767047 | ||||||
| chr12:121767116
|
A | G | 22 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0003g0148others(19): Show | 22 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.552-3791A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767116 | ||||||
| chr12:121767204
|
A | G | 17 | a0001c0001t0001g0272a0001c0001t0006g0033a0001c0001t0006g0049others(14): Show | 17 | HG00621.hp1 HG02040.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.552-3703A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767204 | ||||||
| chr12:121767439
|
C | T | 2 | a0004c0005t0064g0282a0004c0005t0073g0281 | 2 | NA18951.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.552-3468C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767439 | ||||||
| chr12:121767447
|
A | G | 146 | a0001c0001t0001g0104a0001c0001t0001g0129a0001c0001t0001g0176others(143): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.552-3460A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767447 | ||||||
| chr12:121767699
|
G | C | 22 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0003g0148others(19): Show | 22 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.552-3208G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767699 | ||||||
| chr12:121767863
|
G | T | 4 | a0001c0001t0001g0185a0001c0001t0043g0310a0001c0001t0044g0312others(1): Show | 4 | HG03927.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-3044G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767863 | ||||||
| chr12:121767868
|
G | C | 1 | a0001c0001t0006g0267 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.552-3039G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767868 | ||||||
| chr12:121767960
|
T | C | 26 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0001g0185others(23): Show | 26 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.552-2947T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121767960 | ||||||
| chr12:121768476
|
C | T | 1 | a0002c0002t0039g0111 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.552-2431C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768476 | ||||||
| chr12:121768491
|
C | T | 35 | a0001c0001t0001g0272a0001c0001t0002g0020a0001c0001t0002g0021others(32): Show | 35 | HG00621.hp1 HG01099.hp1 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.552-2416C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768491 | ||||||
| chr12:121768534
|
G | C | 1 | a0001c0001t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.552-2373G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768534 | ||||||
| chr12:121768535
|
C | T | 2 | a0001c0001t0005g0025a0001c0001t0006g0051 | 2 | HG02135.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.552-2372C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768535 | ||||||
| chr12:121768572
|
G | T | 7 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.552-2335G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768572 | ||||||
| chr12:121768751
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.552-2156G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768751 | ||||||
| chr12:121768782
|
T | C | 7 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.552-2125T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768782 | ||||||
| chr12:121768812
|
T | TG | 10 | a0001c0001t0002g0136a0001c0001t0003g0148a0001c0001t0003g0180others(7): Show | 10 | HG01109.hp2 HG01358.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.552-2089dupG | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121768812 | |||||
| chr12:121768850
|
G | A | 12 | a0001c0001t0001g0185a0001c0001t0005g0042a0001c0001t0020g0122others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.552-2057G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768850 | ||||||
| chr12:121768911
|
C | T | 7 | a0001c0001t0020g0122a0001c0001t0020g0125a0001c0001t0020g0126others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.552-1996C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121768911 | ||||||
| chr12:121769124
|
C | T | 88 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0105others(85): Show | 88 | HG00544.hp2 HG00621.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.552-1783C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769124 | ||||||
| chr12:121769143
|
CA | C | 88 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0105others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.552-1748delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769143 | |||||
| chr12:121769159
|
A | G | 2 | a0001c0001t0025g0271a0001c0001t0072g0100 | 2 | HG01928.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.552-1748A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769159 | ||||||
| chr12:121769160
|
G | A | 4 | a0001c0001t0082g0073a0001c0004t0099g0010a0001c0004t0100g0082others(1): Show | 4 | HG02809.hp2 HG04184.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-1747G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769160 | ||||||
| chr12:121769161
|
G | C | 2 | a0001c0001t0025g0271a0001c0001t0072g0100 | 2 | HG01928.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.552-1746G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769161 | ||||||
| chr12:121769162
|
C | A | 2 | a0001c0001t0025g0271a0001c0001t0072g0100 | 2 | HG01928.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.552-1745C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769162 | ||||||
| chr12:121769162
|
C | G | 4 | a0001c0001t0082g0073a0001c0004t0099g0010a0001c0004t0100g0082others(1): Show | 4 | HG02809.hp2 HG04184.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-1745C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769162 | ||||||
| chr12:121769162
|
CA | C | 23 | a0001c0001t0001g0045a0001c0001t0001g0099a0001c0001t0001g0185others(20): Show | 23 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.552-1734delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769162 | |||||
| chr12:121769162
|
CAA | C | 123 | a0001c0001t0001g0104a0001c0001t0004g0203a0001c0001t0005g0149others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.552-1735_552-1734d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769162 | |||||
| chr12:121769163
|
A | C | 4 | a0001c0001t0082g0073a0001c0004t0099g0010a0001c0004t0100g0082others(1): Show | 4 | HG02809.hp2 HG04184.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-1744A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769163 | ||||||
| chr12:121769173
|
A | C | 1 | a0002c0002t0008g0223 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.552-1734A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769173 | ||||||
| chr12:121769308
|
G | T | 5 | a0001c0001t0011g0002a0001c0001t0011g0102a0001c0001t0011g0110others(2): Show | 5 | HG01433.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.552-1599G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769308 | ||||||
| chr12:121769353
|
C | T | 1 | a0001c0001t0006g0055 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.552-1554C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769353 | ||||||
| chr12:121769375
|
G | C | 1 | a0001c0001t0011g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.552-1532G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769375 | ||||||
| chr12:121769514
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.552-1393G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769514 | ||||||
| chr12:121769540
|
TA | T | 9 | a0001c0001t0001g0006a0001c0001t0003g0247a0001c0001t0003g0248others(6): Show | 9 | HG00140.hp1 HG01261.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.552-1354delA | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769540 | |||||
| chr12:121769572
|
C | T | 2 | a0001c0001t0029g0076a0001c0001t0029g0077 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552-1335C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769572 | ||||||
| chr12:121769573
|
G | A | 1 | a0001c0001t0006g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.552-1334G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769573 | ||||||
| chr12:121769715
|
C | CGT | 3 | a0002c0002t0001g0236a0002c0002t0001g0237a0005c0006t0047g0144 | 3 | HG00738.hp2 HG01071.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.552-1171_552-1170d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769715 | |||||
| chr12:121769715
|
C | CGTGTGTG others(1): Show |
60 | a0001c0001t0001g0079a0001c0001t0001g0105a0001c0001t0001g0118others(57): Show | 60 | HG00558.hp1 HG01099.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.552-1177_552-1170d others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769715 | |||||
| chr12:121769715
|
C | CGTGTGTG others(3): Show |
175 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0001g0104others(172): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.552-1179_552-1170d others(12): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769715 | |||||
| chr12:121769715
|
C | CGTGTGTG others(5): Show |
9 | a0001c0001t0005g0042a0001c0001t0005g0171a0002c0002t0001g0189others(6): Show | 9 | HG00642.hp2 HG02056.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.552-1181_552-1170d others(14): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769715 | |||||
| chr12:121769715
|
CGT | C | 12 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0179others(9): Show | 12 | HG00423.hp2 HG02074.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.552-1171_552-1170d others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769715 | |||||
| chr12:121769715
|
CGTGTGT | C | 5 | a0001c0001t0043g0310a0001c0001t0097g0311a0002c0002t0002g0192others(2): Show | 5 | HG00438.hp1 HG02040.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.552-1175_552-1170d others(8): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 121769715 | |||||
| chr12:121769899
|
G | C | 2 | a0001c0001t0002g0139a0005c0006t0047g0144 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.552-1008G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769899 | ||||||
| chr12:121769903
|
T | A | 1 | a0001c0001t0012g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.552-1004T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121769903 | ||||||
| chr12:121770070
|
T | C | 1 | a0001c0001t0080g0150 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.552-837T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770070 | ||||||
| chr12:121770124
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.552-783G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770124 | ||||||
| chr12:121770236
|
G | C | 11 | a0001c0001t0003g0003a0001c0001t0003g0251a0001c0001t0003g0253others(8): Show | 11 | HG02109.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.552-671G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770236 | ||||||
| chr12:121770380
|
C | T | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.552-527C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770380 | ||||||
| chr12:121770401
|
G | A | 3 | a0002c0002t0016g0009a0002c0002t0016g0286a0002c0002t0053g0064 | 3 | HG02451.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.552-506G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770401 | ||||||
| chr12:121770571
|
C | T | 5 | a0001c0001t0013g0168a0002c0002t0013g0036a0002c0002t0013g0037others(2): Show | 5 | NA18955.hp1 NA18956.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-336C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770571 | ||||||
| chr12:121770583
|
G | A | 1 | a0001c0001t0072g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.552-324G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770583 | ||||||
| chr12:121770586
|
C | T | 155 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0001g0179others(152): Show | 155 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.552-321C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770586 | ||||||
| chr12:121770587
|
G | A | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.552-320G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770587 | ||||||
| chr12:121770635
|
G | T | 1 | a0001c0001t0025g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.552-272G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770635 | ||||||
| chr12:121770732
|
G | A | 3 | a0001c0001t0002g0136a0001c0001t0002g0139a0001c0001t0002g0147 | 3 | HG02896.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.552-175G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770732 | ||||||
| chr12:121770755
|
G | A | 16 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0009g0151others(13): Show | 17 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.552-152G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770755 | ||||||
| chr12:121770800
|
G | A | 1 | a0001c0001t0023g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.552-107G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770800 | ||||||
| chr12:121770861
|
G | T | 3 | a0001c0001t0003g0148a0001c0001t0003g0180a0001c0001t0102g0083 | 3 | HG01109.hp2 HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552-46G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 6/11 | chr12 | 121770861 | ||||||
| chr12:121771019
|
C | G | 1 | a0002c0002t0053g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.617+47C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771019 | ||||||
| chr12:121771060
|
G | A | 22 | a0001c0001t0001g0045a0001c0001t0007g0266a0001c0001t0009g0004others(19): Show | 23 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.617+88G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771060 | ||||||
| chr12:121771062
|
G | A | 10 | a0001c0001t0001g0006a0002c0002t0001g0194a0002c0002t0001g0195others(7): Show | 10 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+90G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771062 | ||||||
| chr12:121771083
|
A | G | 154 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0001g0272others(151): Show | 154 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.617+111A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771083 | ||||||
| chr12:121771127
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0081g0108a0002c0002t0001g0209others(1): Show | 4 | HG00280.hp1 HG00741.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+155G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771127 | ||||||
| chr12:121771335
|
C | T | 9 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0009g0151others(6): Show | 10 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-153C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771335 | ||||||
| chr12:121771397
|
C | T | 2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.618-91C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771397 | ||||||
| chr12:121771427
|
G | A | 43 | a0001c0001t0003g0003a0001c0001t0003g0107a0001c0001t0003g0148others(40): Show | 43 | HG00140.hp1 HG00735.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.618-61G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 7/11 | chr12 | 121771427 | ||||||
| chr12:121771575
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.679+26G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121771575 | ||||||
| chr12:121771707
|
G | A | 103 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(100): Show | 103 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.679+158G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121771707 | ||||||
| chr12:121771806
|
T | C | 1 | a0003c0003t0010g0072 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.679+257T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121771806 | ||||||
| chr12:121771903
|
G | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.679+354G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121771903 | ||||||
| chr12:121772026
|
CCTTTCTT others(7): Show |
C | 72 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(69): Show | 72 | HG00438.hp1 HG00597.hp2 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.679+492_679+505del others(14): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772026 | |||||
| chr12:121772041
|
C | T | 4 | a0001c0001t0002g0136a0001c0001t0019g0053a0001c0001t0027g0066others(1): Show | 4 | HG02896.hp1 HG03486.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+492C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772041 | ||||||
| chr12:121772048
|
T | C | 4 | a0001c0001t0002g0136a0001c0001t0019g0053a0001c0001t0027g0066others(1): Show | 4 | HG02896.hp1 HG03486.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+499T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772048 | ||||||
| chr12:121772062
|
C | T | 3 | a0001c0001t0002g0136a0001c0001t0019g0053a0003c0003t0002g0284 | 3 | HG02896.hp1 HG03486.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.679+513C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772062 | ||||||
| chr12:121772069
|
T | C | 3 | a0001c0001t0002g0136a0001c0001t0019g0053a0003c0003t0002g0284 | 3 | HG02896.hp1 HG03486.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.679+520T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772069 | ||||||
| chr12:121772071
|
T | C | 1 | a0001c0001t0027g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.679+522T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772071 | ||||||
| chr12:121772073
|
CTTTCTT | C | 3 | a0001c0001t0002g0136a0001c0001t0019g0053a0003c0003t0002g0284 | 3 | HG02896.hp1 HG03486.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.679+526_679+531del others(6): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772073 | |||||
| chr12:121772079
|
T | C | 1 | a0001c0001t0027g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.679+530T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772079 | ||||||
| chr12:121772085
|
T | C | 4 | a0001c0001t0002g0136a0001c0001t0019g0053a0001c0001t0027g0066others(1): Show | 4 | HG02896.hp1 HG03486.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+536T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772085 | ||||||
| chr12:121772085
|
TTCTC | T | 70 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0003g0003others(67): Show | 70 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.679+548_679+551del others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772085 | |||||
| chr12:121772091
|
C | CTCTCTCT others(3): Show |
1 | a0003c0003t0010g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.679+550_679+559dup others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772091 | |||||
| chr12:121772091
|
C | T | 1 | a0001c0001t0027g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.679+542C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772091 | ||||||
| chr12:121772093
|
C | T | 3 | a0001c0001t0002g0136a0001c0001t0019g0053a0003c0003t0002g0284 | 3 | HG02896.hp1 HG03486.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.679+544C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772093 | ||||||
| chr12:121772097
|
CTCTT | C | 8 | a0001c0001t0009g0004a0001c0001t0009g0005a0001c0001t0009g0151others(5): Show | 9 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.679+552_679+555del others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772097 | |||||
| chr12:121772101
|
T | TTCTCTCT others(3): Show |
1 | a0002c0002t0002g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.679+559_679+560ins others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772101 | |||||
| chr12:121772104
|
T | C | 1 | a0001c0001t0007g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.679+555T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772104 | ||||||
| chr12:121772109
|
T | C | 8 | a0001c0001t0002g0136a0001c0001t0006g0051a0001c0001t0019g0053others(5): Show | 8 | HG02135.hp1 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.679+560T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772109 | ||||||
| chr12:121772109
|
T | TTCTCTCT others(1): Show |
69 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(66): Show | 69 | HG00438.hp1 HG00597.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.679+568_679+575dup others(8): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772109 | |||||
| chr12:121772109
|
T | TTCTCTCT others(3): Show |
1 | a0001c0001t0071g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.679+566_679+575dup others(10): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772109 | |||||
| chr12:121772129
|
C | CTCTT | 28 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0005g0040others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.679+596_679+599dup others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772129 | |||||
| chr12:121772156
|
T | A | 1 | a0002c0002t0003g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.679+607T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772156 | ||||||
| chr12:121772184
|
A | G | 1 | a0001c0001t0008g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.679+635A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772184 | ||||||
| chr12:121772190
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.679+641G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772190 | ||||||
| chr12:121772232
|
G | A | 78 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(75): Show | 78 | HG00438.hp1 HG00597.hp2 HG01099.hp1 others(75): Show |
intron_variant | MODIFIER | c.679+683G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772232 | ||||||
| chr12:121772259
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0007g0266a0001c0001t0015g0096others(6): Show | 9 | HG02698.hp2 HG03688.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.679+710G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772259 | ||||||
| chr12:121772424
|
C | T | 3 | a0001c0001t0019g0029a0001c0001t0019g0034a0001c0001t0019g0053 | 3 | NA18960.hp1 NA18994.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.679+875C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772424 | ||||||
| chr12:121772430
|
GTTTC | G | 19 | a0001c0001t0001g0045a0001c0001t0007g0266a0001c0001t0009g0004others(16): Show | 20 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.679+889_679+892del others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772430 | |||||
| chr12:121772438
|
C | CT | 7 | a0001c0001t0005g0081a0001c0001t0033g0135a0001c0001t0033g0145others(4): Show | 7 | HG01261.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+904dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772438 | |||||
| chr12:121772438
|
CT | C | 9 | a0001c0001t0006g0055a0001c0001t0020g0126a0001c0001t0025g0264others(6): Show | 9 | HG01169.hp1 HG01169.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+904delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 121772438 | |||||
| chr12:121772497
|
G | A | 4 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-924G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772497 | ||||||
| chr12:121772519
|
T | A | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.680-902T>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772519 | ||||||
| chr12:121772530
|
G | A | 1 | a0001c0001t0079g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.680-891G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772530 | ||||||
| chr12:121772567
|
G | A | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.680-854G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772567 | ||||||
| chr12:121772586
|
G | A | 2 | a0001c0001t0001g0104a0002c0002t0001g0238 | 2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.680-835G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772586 | ||||||
| chr12:121772591
|
C | G | 107 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.680-830C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772591 | ||||||
| chr12:121772657
|
A | T | 1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.680-764A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772657 | ||||||
| chr12:121772800
|
A | G | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.680-621A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772800 | ||||||
| chr12:121772882
|
A | G | 1 | a0001c0001t0066g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.680-539A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121772882 | ||||||
| chr12:121773327
|
A | G | 1 | a0001c0001t0006g0267 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.680-94A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121773327 | ||||||
| chr12:121773362
|
G | A | 5 | a0001c0001t0001g0129a0002c0002t0001g0239a0002c0002t0001g0243others(2): Show | 5 | HG02027.hp1 HG02056.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.680-59G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 8/11 | chr12 | 121773362 | ||||||
| chr12:121773520
|
A | T | 1 | a0001c0001t0005g0025 | 1 | HG03491.hp1 | splice_region_variant&intron_variant | LOW | c.772+7A>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773520 | ||||||
| chr12:121773579
|
G | T | 1 | a0002c0002t0104g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.772+66G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773579 | ||||||
| chr12:121773619
|
C | T | 1 | a0001c0001t0005g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.772+106C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773619 | ||||||
| chr12:121773716
|
G | T | 8 | a0002c0002t0014g0127a0002c0002t0014g0196a0002c0002t0014g0198others(5): Show | 8 | HG01071.hp2 HG01255.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+203G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773716 | ||||||
| chr12:121773767
|
T | TACACACA others(7): Show |
3 | a0001c0001t0019g0029a0001c0001t0019g0034a0001c0001t0019g0053 | 3 | NA18960.hp1 NA18994.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.772+265_772+266ins others(14): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773767 | |||||
| chr12:121773767
|
T | TACACACA others(9): Show |
133 | a0001c0001t0001g0092a0001c0001t0002g0020a0001c0001t0002g0021others(130): Show | 133 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.772+265_772+266ins others(16): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773767 | |||||
| chr12:121773767
|
T | TACACACA others(11): Show |
7 | a0001c0001t0001g0268a0001c0001t0005g0008a0001c0001t0054g0093others(4): Show | 7 | HG02040.hp1 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.772+265_772+266ins others(18): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773767 | |||||
| chr12:121773767
|
T | TACACACA others(23): Show |
1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.772+265_772+266ins others(30): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773767 | |||||
| chr12:121773876
|
A | G | 170 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0001g0268others(167): Show | 171 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.772+363A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773876 | ||||||
| chr12:121773902
|
A | C | 105 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(102): Show | 105 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.772+389A>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773902 | ||||||
| chr12:121773929
|
G | A | 1 | a0001c0001t0109g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.772+416G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773929 | ||||||
| chr12:121773936
|
A | G | 1 | a0002c0002t0009g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.772+423A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773936 | ||||||
| chr12:121773940
|
AACTCTGC others(10): Show |
A | 2 | a0001c0001t0040g0259a0001c0001t0040g0260 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.772+428_772+444del others(17): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773940 | ||||||
| chr12:121773951
|
C | CT | 6 | a0001c0001t0001g0045a0001c0001t0025g0265a0001c0001t0109g0182others(3): Show | 6 | HG01109.hp1 HG02004.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+462dupT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773951 | |||||
| chr12:121773951
|
CT | C | 49 | a0001c0001t0001g0179a0001c0001t0001g0277a0001c0001t0003g0003others(46): Show | 49 | HG00140.hp1 HG00735.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.772+462delT | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773951 | |||||
| chr12:121773951
|
CTT | C | 10 | a0001c0001t0003g0255a0001c0001t0005g0025a0001c0001t0043g0310others(7): Show | 10 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.772+461_772+462del others(2): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773951 | |||||
| chr12:121773951
|
CTTT | C | 86 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(83): Show | 86 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.772+460_772+462del others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773951 | |||||
| chr12:121773951
|
CTTTT | C | 6 | a0001c0001t0002g0139a0001c0001t0006g0117a0001c0001t0019g0029others(3): Show | 6 | HG01169.hp2 HG02083.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+459_772+462del others(4): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121773951 | |||||
| chr12:121773981
|
G | A | 5 | a0001c0001t0026g0015a0001c0001t0026g0016a0001c0001t0110g0014others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.772+468G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121773981 | ||||||
| chr12:121774000
|
G | A | 8 | a0002c0002t0014g0127a0002c0002t0014g0196a0002c0002t0014g0198others(5): Show | 8 | HG01071.hp2 HG01255.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+487G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774000 | ||||||
| chr12:121774068
|
G | A | 1 | a0001c0001t0008g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.772+555G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774068 | ||||||
| chr12:121774112
|
C | T | 95 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(92): Show | 95 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.773-546C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774112 | ||||||
| chr12:121774117
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0107a0001c0001t0003g0148others(38): Show | 41 | HG00140.hp1 HG00735.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.773-541G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774117 | ||||||
| chr12:121774218
|
C | T | 105 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(102): Show | 105 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.773-440C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774218 | ||||||
| chr12:121774219
|
G | A | 1 | a0001c0001t0003g0300 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.773-439G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774219 | ||||||
| chr12:121774312
|
C | T | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.773-346C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774312 | ||||||
| chr12:121774364
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.773-294T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774364 | ||||||
| chr12:121774469
|
A | G | 105 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(102): Show | 105 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.773-189A>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774469 | ||||||
| chr12:121774558
|
CATCTT | C | 3 | a0001c0001t0035g0133a0001c0001t0035g0134a0001c0001t0078g0132 | 3 | HG02559.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.773-98_773-94delTC others(3): Show |
TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 121774558 | |||||
| chr12:121774605
|
G | A | 1 | a0001c0001t0005g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.773-53G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774605 | ||||||
| chr12:121774619
|
C | G | 105 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(102): Show | 105 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.773-39C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774619 | ||||||
| chr12:121774647
|
C | T | 5 | a0001c0001t0021g0011a0001c0001t0021g0013a0001c0001t0021g0288others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.773-11C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 9/11 | chr12 | 121774647 | ||||||
| chr12:121774753
|
C | T | 105 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(102): Show | 105 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.837+31C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 10/11 | chr12 | 121774753 | ||||||
| chr12:121774846
|
G | T | 169 | a0001c0001t0001g0045a0001c0001t0001g0092a0001c0001t0001g0268others(166): Show | 170 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.837+124G>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 10/11 | chr12 | 121774846 | ||||||
| chr12:121774889
|
C | T | 2 | a0001c0001t0043g0310a0001c0001t0044g0312 | 2 | NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.837+167C>T | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 10/11 | chr12 | 121774889 | ||||||
| chr12:121775043
|
C | G | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.838-19C>G | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 10/11 | chr12 | 121775043 | ||||||
| chr12:121775238
|
G | C | 94 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0002g0020others(91): Show | 94 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.906+108G>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/11 | chr12 | 121775238 | ||||||
| chr12:121775267
|
G | A | 1 | a0001c0001t0032g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.906+137G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/11 | chr12 | 121775267 | ||||||
| chr12:121775338
|
C | A | 29 | a0001c0001t0001g0045a0001c0001t0007g0266a0001c0001t0009g0004others(26): Show | 30 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.906+208C>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/11 | chr12 | 121775338 | ||||||
| chr12:121775387
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.907-222T>C | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/11 | chr12 | 121775387 | ||||||
| chr12:121775445
|
G | A | 1 | a0005c0006t0047g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.907-164G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/11 | chr12 | 121775445 | ||||||
| chr12:121775568
|
G | A | 2 | a0002c0002t0003g0084a0002c0002t0003g0087 | 2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.907-41G>A | TMEM120B | ENSG00000188735.13 | transcript | ENST00000449592.7 | protein_coding | 11/11 | chr12 | 121775568 |