Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23232 |
| ensemblid | ENSG00000108239.9 |
| hgncid | 29082 |
| symbol | TBC1D12 |
| name | TBC1 domain family member 12 |
| refseq_nuc | NM_015188.2 |
| refseq_prot | NP_056003.1 |
| ensembl_nuc | ENST00000225235.5 |
| ensembl_prot | ENSP00000225235.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 94402541 |
| end | 94536332 |
| strand | + |
| ver | v1.2 |
| region | chr10:94402541-94536332 |
| region5000 | chr10:94397541-94541332 |
| regionname0 | TBC1D12_chr10_94402541_94536332 |
| regionname5000 | TBC1D12_chr10_94397541_94541332 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 775 | 342 | 82 | 58 | 139 | 18 | 43 | 99 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | MVGPE others(770): Show |
chr10 | 94397541 | 94541332 |
| a0002 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | MVGPE others(770): Show |
chr10 | 94397541 | 94541332 |
| a0003 | 0/0 | 775 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | MVGPE others(770): Show |
chr10 | 94397541 | 94541332 |
| a0004 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | MVGPE others(770): Show |
chr10 | 94397541 | 94541332 |
| a0005 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | MVGPE others(770): Show |
chr10 | 94397541 | 94541332 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2325 | 234 | 48 | 37 | 106 | 13 | 29 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0001c0002 | 1/0 | 2325 | 100 | 29 | 21 | 30 | 5 | 14 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0001c0003 | 0/0 | 2325 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0001c0004 | 0/0 | 2325 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0001c0007 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0001c0008 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0001c0011 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0002c0006 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0003c0009 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0004c0005 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 | ||
| a0005c0010 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | ATGGT others(2320): Show |
chr10 | 94397541 | 94541332 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5637 | 164 | 31 | 20 | 87 | 7 | 19 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0002 | 0/1 | 5637 | 29 | 2 | 15 | 3 | 4 | 4 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0004 | 0/0 | 5637 | 11 | 0 | 0 | 9 | 0 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0005 | 0/0 | 5637 | 11 | 11 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0006 | 0/0 | 5637 | 6 | 0 | 1 | 3 | 1 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0011 | 0/0 | 5637 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0014 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0015 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0017 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0018 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0019 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0020 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0021 | 0/0 | 5637 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0023 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0024 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0025 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0001t0026 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0002 | 1/0 | 5637 | 55 | 9 | 10 | 28 | 3 | 4 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0003 | 0/0 | 5637 | 34 | 17 | 9 | 2 | 0 | 6 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0007 | 0/0 | 5637 | 5 | 0 | 2 | 0 | 2 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0009 | 0/0 | 5637 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0010 | 0/0 | 5637 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0016 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0002t0022 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0003t0008 | 0/0 | 5637 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0004t0012 | 0/0 | 5637 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0007t0004 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0008t0001 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0001c0011t0001 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0002c0006t0013 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0003c0009t0006 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0004c0005t0002 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| a0005c0010t0001 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | AGAGC others(5632): Show |
chr10 | 94397541 | 94541332 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0014g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0017g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0018g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0019g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0020g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0021g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0023g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0024g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0025g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0026g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0010g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0010g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0016g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0022g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0003t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0003t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0003t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0004t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0004t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0007t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0008t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0011t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0002c0006t0013g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0003c0009t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0004c0005t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0005c0010t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00140 | hp1 | a0001 | c0002 | t0007 | g0320 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00280 | hp2 | a0001 | c0001 | t0023 | g0120 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0295 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00609 | hp2 | a0001 | c0001 | t0014 | g0125 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0321 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0331 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0330 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0326 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0327 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0311 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01168 | hp1 | a0001 | c0002 | t0007 | g0234 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0235 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0303 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0284 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0312 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0336 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0304 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0310 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0236 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0183 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0333 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0317 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02055 | hp2 | a0001 | c0002 | t0022 | g0296 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02071 | hp2 | a0001 | c0007 | t0004 | g0217 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | CDX | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02257 | hp2 | a0002 | c0006 | t0013 | g0344 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02258 | hp1 | a0001 | c0003 | t0008 | g0012 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02258 | hp2 | a0001 | c0004 | t0012 | g0211 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0285 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0230 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0314 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0334 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0340 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0181 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0199 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0302 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02738 | hp2 | a0001 | c0002 | t0007 | g0323 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02922 | hp1 | a0001 | c0003 | t0008 | g0013 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02922 | hp2 | a0001 | c0004 | t0012 | g0212 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0177 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0305 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03017 | hp2 | a0001 | c0001 | t0025 | g0068 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0339 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0182 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0020 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0318 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0329 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0180 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03491 | hp1 | a0001 | c0001 | t0024 | g0056 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03491 | hp2 | a0001 | c0002 | t0010 | g0306 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03492 | hp2 | a0001 | c0002 | t0010 | g0315 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0325 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03540 | hp2 | a0001 | c0002 | t0009 | g0245 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03579 | hp2 | a0001 | c0003 | t0008 | g0014 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0286 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0262 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0322 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0313 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0309 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03710 | hp2 | a0003 | c0009 | t0006 | g0008 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0214 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03942 | hp2 | a0001 | c0002 | t0016 | g0277 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0263 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0193 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0316 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0178 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18943 | hp1 | a0001 | c0008 | t0001 | g0052 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18948 | hp2 | a0004 | c0005 | t0002 | g0256 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18953 | hp1 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18984 | hp1 | a0001 | c0011 | t0001 | g0087 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19000 | hp1 | a0001 | c0001 | t0015 | g0092 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0335 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19072 | hp1 | a0001 | c0001 | t0017 | g0074 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19240 | hp1 | a0005 | c0010 | t0001 | g0185 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0174 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0328 | AFR | ASW | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20752 | hp1 | a0001 | c0002 | t0007 | g0319 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0266 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0007 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | GIH | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20905 | hp2 | a0001 | c0001 | t0026 | g0006 | SAS | GIH | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01123 | hp2 | a0001 | c0001 | t0021 | g0272 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0324 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0179 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0332 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0338 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0307 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0250 | REF | REF | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0337 | REF | REF | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94403373 | G | C | 1 | a0002 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.760G>C | p.Glu254Gln | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 833/5637 | 760/2328 | 254/775 | chr10 | 94403373 | |||
| chr10:94403488 | C | T | 1 | a0002 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.875C>T | p.Ala292Val | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 948/5637 | 875/2328 | 292/775 | chr10 | 94403488 | |||
| chr10:94403512 | C | T | 1 | a0005 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.899C>T | p.Ala300Val | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 972/5637 | 899/2328 | 300/775 | chr10 | 94403512 | |||
| chr10:94403521 | A | G | 1 | a0004 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.908A>G | p.Gln303Arg | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 981/5637 | 908/2328 | 303/775 | chr10 | 94403521 | |||
| chr10:94510168 | A | T | 1 | a0003 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1678A>T | p.Ile560Phe | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/13 | 1751/5637 | 1678/2328 | 560/775 | chr10 | 94510168 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94403222 | C | T | 1 | a0001c0011 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.609C>T | p.Cys203Cys | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 682/5637 | 609/2328 | 203/775 | chr10 | 94403222 | |||
| chr10:94403282 | C | G | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
synonymous_variant | LOW | c.669C>G | p.Pro223Pro | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 742/5637 | 669/2328 | 223/775 | chr10 | 94403282 | |||
| chr10:94403387 | G | C | 1 | a0001c0007 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.774G>C | p.Gly258Gly | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 847/5637 | 774/2328 | 258/775 | chr10 | 94403387 | |||
| chr10:94500266 | C | T | 1 | a0001c0003 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1458C>T | p.Pro486Pro | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/13 | 1531/5637 | 1458/2328 | 486/775 | chr10 | 94500266 | |||
| chr10:94511624 | A | G | 1 | a0001c0004 | 2 | HG02258.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.1731A>G | p.Ala577Ala | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/13 | 1804/5637 | 1731/2328 | 577/775 | chr10 | 94511624 | |||
| chr10:94533066 | C | T | 1 | a0001c0008 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.2298C>T | p.Asp766Asp | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2371/5637 | 2298/2328 | 766/775 | chr10 | 94533066 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94402563 | T | G | 1 | a0002c0006t0013 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 51 | chr10 | 94402563 | ||||||
| chr10:94533231 | T | A | 4 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0009 others(1): Show |
43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*135T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 135 | chr10 | 94533231 | ||||||
| chr10:94533407 | A | C | 3 | a0001c0001t0006 a0001c0001t0026 a0003c0009t0006 |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*311A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 311 | chr10 | 94533407 | ||||||
| chr10:94533630 | C | T | 1 | a0001c0001t0025 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 534 | chr10 | 94533630 | ||||||
| chr10:94533631 | G | A | 1 | a0002c0006t0013 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*535G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 535 | chr10 | 94533631 | ||||||
| chr10:94533747 | A | G | 3 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0010 |
41 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*651A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 651 | chr10 | 94533747 | ||||||
| chr10:94533929 | G | A | 1 | a0001c0002t0009 | 2 | HG02615.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*833G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 833 | chr10 | 94533929 | ||||||
| chr10:94534003 | A | G | 1 | a0001c0001t0024 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 907 | chr10 | 94534003 | ||||||
| chr10:94534021 | T | A | 1 | a0001c0001t0005 | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*925T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 925 | chr10 | 94534021 | ||||||
| chr10:94534093 | A | C | 1 | a0001c0001t0023 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*997A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 997 | chr10 | 94534093 | ||||||
| chr10:94534333 | C | T | 1 | a0001c0004t0012 | 2 | HG02258.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1237C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1237 | chr10 | 94534333 | ||||||
| chr10:94534334 | G | A | 1 | a0001c0001t0014 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1238 | chr10 | 94534334 | ||||||
| chr10:94534499 | T | A | 1 | a0001c0002t0010 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1403T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1403 | chr10 | 94534499 | ||||||
| chr10:94534585 | G | C | 1 | a0001c0001t0015 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1489 | chr10 | 94534585 | ||||||
| chr10:94534634 | G | A | 1 | a0001c0002t0016 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1538G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1538 | chr10 | 94534634 | ||||||
| chr10:94534755 | C | T | 1 | a0001c0003t0008 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1659C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1659 | chr10 | 94534755 | ||||||
| chr10:94534852 | A | G | 1 | a0001c0001t0011 | 2 | HG02717.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1756A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1756 | chr10 | 94534852 | ||||||
| chr10:94534933 | T | C | 1 | a0001c0001t0005 | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1837T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1837 | chr10 | 94534933 | ||||||
| chr10:94535094 | T | C | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(20): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1998T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1998 | chr10 | 94535094 | ||||||
| chr10:94535115 | T | C | 1 | a0001c0001t0026 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2019T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2019 | chr10 | 94535115 | ||||||
| chr10:94535201 | G | C | 1 | a0001c0001t0017 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2105G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2105 | chr10 | 94535201 | ||||||
| chr10:94535222 | T | G | 1 | a0001c0001t0011 | 2 | HG02717.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2126T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2126 | chr10 | 94535222 | ||||||
| chr10:94535277 | T | A | 1 | a0001c0001t0005 | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2181T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2181 | chr10 | 94535277 | ||||||
| chr10:94535303 | T | C | 1 | a0001c0001t0018 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2207T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2207 | chr10 | 94535303 | ||||||
| chr10:94535408 | A | G | 2 | a0001c0001t0004 a0001c0007t0004 |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2312A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2312 | chr10 | 94535408 | ||||||
| chr10:94535565 | A | G | 1 | a0001c0001t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2469 | chr10 | 94535565 | ||||||
| chr10:94535770 | A | C | 1 | a0001c0002t0007 | 5 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2674A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2674 | chr10 | 94535770 | ||||||
| chr10:94535799 | T | C | 1 | a0001c0001t0021 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2703T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2703 | chr10 | 94535799 | ||||||
| chr10:94536060 | T | C | 2 | a0001c0001t0011 a0001c0001t0019 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2964T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2964 | chr10 | 94536060 | ||||||
| chr10:94536216 | A | C | 1 | a0001c0002t0022 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 3120 | chr10 | 94536216 | ||||||
| chr10:94536305 | C | T | 1 | a0001c0001t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3209C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 3209 | chr10 | 94536305 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94403589 | A | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.971+5A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403589 | |||||||
| chr10:94403618 | T | TCCGGGG | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+45_971+50dupGG others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94403618 | ||||||
| chr10:94403627 | G | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+43G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403627 | |||||||
| chr10:94403655 | T | TCGGAGC | 170 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.971+90_971+95dupCG others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94403655 | ||||||
| chr10:94403706 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.971+122C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403706 | |||||||
| chr10:94403766 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.971+182C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403766 | |||||||
| chr10:94403868 | T | G | 11 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.971+284T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403868 | |||||||
| chr10:94403915 | CT | C | 16 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+335delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94403915 | ||||||
| chr10:94404007 | C | G | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971+423C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404007 | |||||||
| chr10:94404041 | G | A | 198 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.971+457G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404041 | |||||||
| chr10:94404231 | G | C | 336 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(333): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.971+647G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404231 | |||||||
| chr10:94404231 | G | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+647G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404231 | |||||||
| chr10:94404272 | A | G | 16 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(13): Show |
17 | HG01884.hp2 HG02071.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.971+688A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404272 | |||||||
| chr10:94404309 | T | A | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.971+725T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404309 | |||||||
| chr10:94404310 | A | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+726A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404310 | |||||||
| chr10:94404600 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.971+1016C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404600 | |||||||
| chr10:94404648 | C | CA | 9 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(6): Show |
9 | HG01978.hp1 HG03490.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.971+1079dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94404648 | ||||||
| chr10:94404648 | CA | C | 170 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(167): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.971+1079delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94404648 | ||||||
| chr10:94404775 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.971+1191T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404775 | |||||||
| chr10:94404812 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00673.hp2 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.971+1228C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404812 | |||||||
| chr10:94405001 | C | A | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.971+1417C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405001 | |||||||
| chr10:94405042 | C | G | 1 | a0001c0002t0003g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.971+1458C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405042 | |||||||
| chr10:94405046 | C | CA | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0002g0002 others(15): Show |
19 | HG00639.hp1 HG01433.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.971+1479dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405046 | ||||||
| chr10:94405046 | CA | C | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.971+1479delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405046 | ||||||
| chr10:94405094 | G | A | 2 | a0001c0002t0002g0232 a0001c0002t0002g0233 |
2 | HG02056.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.971+1510G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405094 | |||||||
| chr10:94405117 | C | T | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.971+1533C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405117 | |||||||
| chr10:94405206 | C | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+1622C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405206 | |||||||
| chr10:94405479 | T | C | 2 | a0001c0002t0007g0234 a0001c0002t0007g0235 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.971+1895T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405479 | |||||||
| chr10:94405690 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG01358.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.971+2106C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405690 | |||||||
| chr10:94405732 | C | T | 2 | a0001c0002t0002g0332 a0001c0002t0002g0333 |
2 | HG01928.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.971+2148C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405732 | |||||||
| chr10:94405812 | A | AT | 7 | a0001c0002t0002g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+2243dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405812 | ||||||
| chr10:94405812 | AT | A | 87 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.971+2243delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405812 | ||||||
| chr10:94405828 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.971+2244G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405828 | |||||||
| chr10:94405901 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.971+2317C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405901 | |||||||
| chr10:94405961 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+2377C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405961 | |||||||
| chr10:94405965 | C | G | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.971+2381C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405965 | |||||||
| chr10:94405983 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.971+2399G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405983 | |||||||
| chr10:94406225 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.971+2641T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406225 | |||||||
| chr10:94406310 | T | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+2726T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406310 | |||||||
| chr10:94406402 | C | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+2818C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406402 | |||||||
| chr10:94406721 | C | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.971+3137C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406721 | |||||||
| chr10:94406772 | G | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+3188G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406772 | |||||||
| chr10:94406967 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.971+3383A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406967 | |||||||
| chr10:94407008 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.971+3424G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407008 | |||||||
| chr10:94407054 | T | TAA | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+3479_971+3480d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407054 | ||||||
| chr10:94407054 | TA | T | 41 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(38): Show |
41 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.971+3480delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407054 | ||||||
| chr10:94407145 | C | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18950.hp2 NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.971+3561C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407145 | |||||||
| chr10:94407171 | A | T | 199 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.971+3587A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407171 | |||||||
| chr10:94407278 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.971+3694G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407278 | |||||||
| chr10:94407421 | C | CCT | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+3838_971+3839d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407421 | ||||||
| chr10:94407453 | G | A | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.971+3869G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407453 | |||||||
| chr10:94407675 | C | CA | 201 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(198): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.971+4105dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407675 | ||||||
| chr10:94407675 | C | CG | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.971+4091_971+4092i others(3): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407675 | |||||||
| chr10:94407797 | C | T | 1 | a0001c0002t0003g0325 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.971+4213C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407797 | |||||||
| chr10:94407985 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.971+4401G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407985 | |||||||
| chr10:94408001 | C | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+4417C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408001 | |||||||
| chr10:94408378 | A | G | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.971+4794A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408378 | |||||||
| chr10:94408562 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.971+4978A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408562 | |||||||
| chr10:94408644 | A | G | 65 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(62): Show |
65 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.971+5060A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408644 | |||||||
| chr10:94408850 | C | T | 2 | a0001c0002t0003g0230 a0001c0002t0003g0324 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.971+5266C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408850 | |||||||
| chr10:94408986 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.971+5402C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408986 | |||||||
| chr10:94409087 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+5503T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409087 | |||||||
| chr10:94409173 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+5589G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409173 | |||||||
| chr10:94409219 | A | G | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.971+5635A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409219 | |||||||
| chr10:94409225 | G | A | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.971+5641G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409225 | |||||||
| chr10:94409374 | C | CT | 164 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.971+5810dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94409374 | ||||||
| chr10:94409374 | C | CTT | 7 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0098 others(4): Show |
7 | HG00438.hp2 HG02257.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+5809_971+5810d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94409374 | ||||||
| chr10:94409389 | T | G | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.971+5805T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409389 | |||||||
| chr10:94409403 | A | C | 1 | a0001c0002t0002g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.971+5819A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409403 | |||||||
| chr10:94409447 | C | T | 1 | a0001c0002t0003g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.971+5863C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409447 | |||||||
| chr10:94409498 | A | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG00099.hp1 HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.971+5914A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409498 | |||||||
| chr10:94409664 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+6080C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409664 | |||||||
| chr10:94409862 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+6278A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409862 | |||||||
| chr10:94410448 | C | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+6864C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94410448 | |||||||
| chr10:94410746 | G | T | 1 | a0001c0002t0002g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.971+7162G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94410746 | |||||||
| chr10:94410836 | A | G | 199 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.971+7252A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94410836 | |||||||
| chr10:94411349 | A | G | 271 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.971+7765A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411349 | |||||||
| chr10:94411543 | C | A | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.971+7959C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411543 | |||||||
| chr10:94411717 | C | G | 16 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(13): Show |
17 | HG01884.hp2 HG02071.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.971+8133C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411717 | |||||||
| chr10:94411730 | G | A | 1 | a0001c0002t0002g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.971+8146G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411730 | |||||||
| chr10:94412262 | A | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+8678A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412262 | |||||||
| chr10:94412506 | G | A | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.971+8922G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412506 | |||||||
| chr10:94412532 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+8948A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412532 | |||||||
| chr10:94412636 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.971+9052G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412636 | |||||||
| chr10:94412717 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.971+9133G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412717 | |||||||
| chr10:94412807 | C | G | 14 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0094 others(11): Show |
15 | HG02027.hp1 HG02071.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.971+9223C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412807 | |||||||
| chr10:94412993 | G | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+9409G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412993 | |||||||
| chr10:94413356 | T | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+9772T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413356 | |||||||
| chr10:94413443 | T | G | 13 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(10): Show |
14 | HG02071.hp2 HG03225.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.971+9859T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413443 | |||||||
| chr10:94413547 | C | T | 46 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(43): Show |
46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.971+9963C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413547 | |||||||
| chr10:94413711 | A | C | 3 | a0001c0002t0002g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 |
3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.971+10127A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413711 | |||||||
| chr10:94413881 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.971+10297G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413881 | |||||||
| chr10:94414159 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.971+10575C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414159 | |||||||
| chr10:94414200 | T | C | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.971+10616T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414200 | |||||||
| chr10:94414215 | A | G | 196 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.971+10631A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414215 | |||||||
| chr10:94414347 | C | T | 37 | a0001c0001t0001g0017 a0001c0001t0001g0077 a0001c0001t0001g0078 others(34): Show |
37 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.971+10763C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414347 | |||||||
| chr10:94414391 | T | C | 2 | a0001c0002t0003g0302 a0001c0002t0003g0303 |
2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.971+10807T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414391 | |||||||
| chr10:94414437 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+10853C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414437 | |||||||
| chr10:94414600 | C | CT | 250 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.971+11033dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94414600 | ||||||
| chr10:94414600 | C | CTT | 16 | a0001c0001t0001g0076 a0001c0001t0001g0130 a0001c0001t0005g0200 others(13): Show |
16 | HG02040.hp1 HG02080.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+11032_971+1103 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94414600 | ||||||
| chr10:94414662 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.971+11078C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414662 | |||||||
| chr10:94414814 | G | A | 77 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.971+11230G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414814 | |||||||
| chr10:94414851 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+11267C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414851 | |||||||
| chr10:94414852 | G | A | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.971+11268G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414852 | |||||||
| chr10:94415228 | A | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+11644A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415228 | |||||||
| chr10:94415549 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.971+11965C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415549 | |||||||
| chr10:94415745 | C | CA | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG00597.hp1 NA18612.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.971+12169dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94415745 | ||||||
| chr10:94415763 | A | C | 1 | a0001c0001t0004g0221 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.971+12179A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415763 | |||||||
| chr10:94415950 | G | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+12366G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415950 | |||||||
| chr10:94415975 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+12391A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415975 | |||||||
| chr10:94416105 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+12521A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416105 | |||||||
| chr10:94416112 | G | GA | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+12536dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94416112 | ||||||
| chr10:94416164 | G | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+12580G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416164 | |||||||
| chr10:94416255 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.971+12671T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416255 | |||||||
| chr10:94416389 | G | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+12805G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416389 | |||||||
| chr10:94416425 | T | C | 4 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.971+12841T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416425 | |||||||
| chr10:94416619 | T | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.971+13035T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416619 | |||||||
| chr10:94416896 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+13312G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416896 | |||||||
| chr10:94416992 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.971+13408A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416992 | |||||||
| chr10:94417634 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.971+14050A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417634 | |||||||
| chr10:94417725 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+14141C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417725 | |||||||
| chr10:94417745 | T | C | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+14161T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417745 | |||||||
| chr10:94417750 | C | CT | 27 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(24): Show |
28 | HG01884.hp2 HG02071.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.971+14182dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94417750 | ||||||
| chr10:94417750 | CT | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(160): Show |
163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.971+14182delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94417750 | ||||||
| chr10:94417760 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0094 |
2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.971+14176T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417760 | |||||||
| chr10:94417771 | C | T | 2 | a0001c0002t0002g0294 a0001c0002t0002g0295 |
2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.971+14187C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417771 | |||||||
| chr10:94417806 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.971+14222T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417806 | |||||||
| chr10:94417813 | G | A | 213 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.971+14229G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417813 | |||||||
| chr10:94417867 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.971+14283C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417867 | |||||||
| chr10:94417882 | T | TG | 197 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.971+14300dupG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94417882 | ||||||
| chr10:94417958 | G | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+14374G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417958 | |||||||
| chr10:94417982 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+14398C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417982 | |||||||
| chr10:94418171 | CTTGGGCC others(15): Show |
C | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.971+14592_971+1461 others(26): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418171 | ||||||
| chr10:94418238 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.971+14654C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418238 | |||||||
| chr10:94418478 | T | C | 9 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(6): Show |
9 | HG01074.hp1 HG01257.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+14894T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418478 | |||||||
| chr10:94418530 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0084 |
2 | HG00673.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.971+14946C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418530 | |||||||
| chr10:94418555 | C | CTAT | 20 | a0001c0001t0001g0184 a0001c0001t0001g0196 a0001c0001t0001g0197 others(17): Show |
21 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.971+14996_971+1499 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | ||||||
| chr10:94418555 | C | CTATTAT | 10 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(7): Show |
11 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+14993_971+1499 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | ||||||
| chr10:94418555 | C | CTATTATT others(2): Show |
5 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(2): Show |
5 | HG01884.hp2 HG02257.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+14990_971+1499 others(13): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | ||||||
| chr10:94418555 | C | CTATTATT others(5): Show |
1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.971+14987_971+1499 others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | ||||||
| chr10:94418555 | CTAT | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0006g0003 others(7): Show |
10 | HG01978.hp1 HG03490.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.971+14996_971+1499 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | ||||||
| chr10:94418577 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.971+14993T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418577 | |||||||
| chr10:94418580 | T | A | 152 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.971+14996T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418580 | |||||||
| chr10:94418936 | G | T | 3 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 |
3 | HG00642.hp1 HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.971+15352G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418936 | |||||||
| chr10:94418937 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+15353C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418937 | |||||||
| chr10:94418967 | T | G | 1 | a0001c0002t0022g0296 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.971+15383T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418967 | |||||||
| chr10:94419116 | A | G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+15532A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419116 | |||||||
| chr10:94419164 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.971+15580C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419164 | |||||||
| chr10:94419208 | T | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+15624T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419208 | |||||||
| chr10:94419260 | C | T | 1 | a0001c0002t0003g0182 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.971+15676C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419260 | |||||||
| chr10:94419533 | C | T | 16 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+15949C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419533 | |||||||
| chr10:94419567 | A | G | 2 | a0001c0002t0009g0245 a0001c0002t0009g0334 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.971+15983A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419567 | |||||||
| chr10:94419625 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.971+16041C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419625 | |||||||
| chr10:94419970 | G | C | 16 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+16386G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419970 | |||||||
| chr10:94420007 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.971+16423G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420007 | |||||||
| chr10:94420296 | G | T | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.971+16712G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420296 | |||||||
| chr10:94420325 | T | C | 1 | a0001c0002t0009g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.971+16741T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420325 | |||||||
| chr10:94420345 | T | C | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.971+16761T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420345 | |||||||
| chr10:94420436 | A | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+16852A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420436 | |||||||
| chr10:94420443 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+16859A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420443 | |||||||
| chr10:94420448 | G | T | 2 | a0001c0002t0002g0290 a0001c0002t0002g0291 |
2 | NA18953.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.971+16864G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420448 | |||||||
| chr10:94420473 | C | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+16889C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420473 | |||||||
| chr10:94420603 | A | G | 20 | a0001c0001t0001g0078 a0001c0001t0001g0093 a0001c0001t0001g0143 others(17): Show |
20 | HG00438.hp2 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.971+17019A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420603 | |||||||
| chr10:94420639 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0083 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.971+17055T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420639 | |||||||
| chr10:94420789 | C | T | 1 | a0001c0001t0004g0220 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.971+17205C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420789 | |||||||
| chr10:94420834 | G | GT | 3 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0086 |
3 | HG02040.hp2 NA18983.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.971+17255dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94420834 | ||||||
| chr10:94420921 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.971+17337T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420921 | |||||||
| chr10:94421192 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+17608C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421192 | |||||||
| chr10:94421439 | G | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.971+17855G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421439 | |||||||
| chr10:94421555 | T | C | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.971+17971T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421555 | |||||||
| chr10:94421867 | A | T | 3 | a0001c0002t0002g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 |
3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.971+18283A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421867 | |||||||
| chr10:94421944 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.971+18360A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421944 | |||||||
| chr10:94422085 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.971+18501G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422085 | |||||||
| chr10:94422151 | T | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+18567T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422151 | |||||||
| chr10:94422185 | G | GT | 40 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0099 others(37): Show |
40 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.971+18624dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94422185 | ||||||
| chr10:94422185 | GT | G | 72 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.971+18624delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94422185 | ||||||
| chr10:94422189 | T | G | 1 | a0001c0001t0006g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.971+18605T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422189 | |||||||
| chr10:94422352 | G | C | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971+18768G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422352 | |||||||
| chr10:94422974 | C | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-18922C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422974 | |||||||
| chr10:94423132 | T | TAAAGG | 195 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.972-18760_972-1875 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94423132 | ||||||
| chr10:94423183 | C | T | 198 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.972-18713C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423183 | |||||||
| chr10:94423246 | T | C | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.972-18650T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423246 | |||||||
| chr10:94423267 | G | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.972-18629G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423267 | |||||||
| chr10:94423342 | C | CT | 231 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.972-18532dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94423342 | ||||||
| chr10:94423342 | C | CTT | 23 | a0001c0001t0001g0032 a0001c0001t0001g0100 a0001c0001t0001g0126 others(20): Show |
24 | HG00423.hp1 HG00597.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.972-18533_972-1853 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94423342 | ||||||
| chr10:94423488 | C | T | 1 | a0001c0002t0002g0282 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.972-18408C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423488 | |||||||
| chr10:94423544 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-18352C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423544 | |||||||
| chr10:94423594 | T | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.972-18302T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423594 | |||||||
| chr10:94423595 | G | A | 5 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 others(2): Show |
5 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.972-18301G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423595 | |||||||
| chr10:94423705 | G | A | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.972-18191G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423705 | |||||||
| chr10:94423714 | G | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.972-18182G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423714 | |||||||
| chr10:94423812 | C | T | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.972-18084C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423812 | |||||||
| chr10:94423819 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-18077A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423819 | |||||||
| chr10:94424051 | ATAAT | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-17840_972-1783 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94424051 | ||||||
| chr10:94424074 | A | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02300.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.972-17822A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424074 | |||||||
| chr10:94424164 | G | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-17732G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424164 | |||||||
| chr10:94424194 | C | CT | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.972-17702_972-1770 others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424194 | |||||||
| chr10:94424208 | A | G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-17688A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424208 | |||||||
| chr10:94424463 | C | T | 190 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.972-17433C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424463 | |||||||
| chr10:94424507 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0014g0125 |
2 | HG00609.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.972-17389C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424507 | |||||||
| chr10:94424691 | C | T | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.972-17205C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424691 | |||||||
| chr10:94424884 | C | T | 46 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(43): Show |
46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.972-17012C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424884 | |||||||
| chr10:94425040 | G | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.972-16856G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425040 | |||||||
| chr10:94425376 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.972-16520C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425376 | |||||||
| chr10:94425458 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-16438A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425458 | |||||||
| chr10:94425588 | G | GT | 12 | a0001c0001t0002g0025 a0001c0001t0005g0200 a0001c0001t0005g0201 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.972-16299dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94425588 | ||||||
| chr10:94425833 | A | G | 198 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.972-16063A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425833 | |||||||
| chr10:94425937 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-15959T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425937 | |||||||
| chr10:94426014 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-15882C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426014 | |||||||
| chr10:94426082 | A | T | 1 | a0001c0002t0003g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.972-15814A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426082 | |||||||
| chr10:94426664 | G | A | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.972-15232G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426664 | |||||||
| chr10:94426738 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-15158G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426738 | |||||||
| chr10:94426955 | A | G | 65 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(62): Show |
65 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.972-14941A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426955 | |||||||
| chr10:94427044 | C | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-14852C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427044 | |||||||
| chr10:94427056 | A | G | 2 | a0001c0001t0004g0001 a0001c0001t0004g0219 |
3 | NA18948.hp1 NA18979.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.972-14840A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427056 | |||||||
| chr10:94427265 | G | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-14631G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427265 | |||||||
| chr10:94427504 | G | A | 1 | a0001c0002t0002g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.972-14392G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427504 | |||||||
| chr10:94427565 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-14331C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427565 | |||||||
| chr10:94427569 | C | T | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-14327C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427569 | |||||||
| chr10:94427751 | G | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0239 a0001c0001t0002g0240 others(4): Show |
8 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-14145G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427751 | |||||||
| chr10:94427833 | C | CA | 153 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.972-14039dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94427833 | ||||||
| chr10:94427833 | C | CAA | 38 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(35): Show |
38 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.972-14040_972-1403 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94427833 | ||||||
| chr10:94427833 | CA | C | 50 | a0001c0001t0004g0001 a0001c0001t0004g0215 a0001c0001t0004g0216 others(47): Show |
51 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.972-14039delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94427833 | ||||||
| chr10:94428095 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-13801A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428095 | |||||||
| chr10:94428176 | G | C | 2 | a0001c0002t0002g0294 a0001c0002t0002g0295 |
2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.972-13720G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428176 | |||||||
| chr10:94428282 | C | CT | 67 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0089 others(64): Show |
68 | HG00140.hp1 HG00423.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.972-13591dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94428282 | ||||||
| chr10:94428282 | C | CTT | 16 | a0001c0001t0001g0100 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG01192.hp1 HG02015.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.972-13592_972-1359 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94428282 | ||||||
| chr10:94428282 | CT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0128 a0001c0001t0001g0167 others(8): Show |
11 | HG01167.hp2 HG01981.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-13591delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94428282 | ||||||
| chr10:94428305 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.972-13591T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428305 | |||||||
| chr10:94428494 | G | C | 214 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.972-13402G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428494 | |||||||
| chr10:94428702 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.972-13194A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428702 | |||||||
| chr10:94428808 | T | C | 215 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.972-13088T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428808 | |||||||
| chr10:94428901 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-12995C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428901 | |||||||
| chr10:94428952 | G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-12944G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428952 | |||||||
| chr10:94429045 | CT | C | 17 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(14): Show |
18 | HG01167.hp2 HG01884.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-12839delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94429045 | ||||||
| chr10:94429245 | A | G | 2 | a0001c0002t0003g0174 a0001c0002t0003g0175 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.972-12651A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429245 | |||||||
| chr10:94429542 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.972-12354T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429542 | |||||||
| chr10:94429562 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.972-12334T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429562 | |||||||
| chr10:94429598 | A | G | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.972-12298A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429598 | |||||||
| chr10:94429949 | C | T | 26 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(23): Show |
27 | HG01884.hp2 HG02071.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.972-11947C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429949 | |||||||
| chr10:94429956 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.972-11940G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429956 | |||||||
| chr10:94430143 | C | T | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.972-11753C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94430143 | |||||||
| chr10:94431026 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-10870A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431026 | |||||||
| chr10:94431323 | G | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.972-10573G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431323 | |||||||
| chr10:94431406 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-10490C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431406 | |||||||
| chr10:94431410 | TA | T | 7 | a0001c0001t0001g0187 a0001c0001t0002g0279 a0001c0001t0004g0218 others(4): Show |
7 | HG00323.hp2 HG01169.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-10471delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94431410 | ||||||
| chr10:94431421 | AAAAAG | A | 150 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0017 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.972-10466_972-1046 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94431421 | ||||||
| chr10:94431520 | G | A | 1 | a0001c0002t0002g0259 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.972-10376G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431520 | |||||||
| chr10:94431566 | G | T | 4 | a0001c0002t0003g0174 a0001c0002t0003g0175 a0001c0002t0003g0180 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-10330G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431566 | |||||||
| chr10:94431783 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.972-10113C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431783 | |||||||
| chr10:94431803 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-10093A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431803 | |||||||
| chr10:94431915 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.972-9981G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431915 | |||||||
| chr10:94431944 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-9952C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431944 | |||||||
| chr10:94432122 | A | AAG | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-9763_972-9762d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94432122 | ||||||
| chr10:94432186 | G | A | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.972-9710G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94432186 | |||||||
| chr10:94432476 | TTA | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0138 a0001c0001t0001g0141 |
3 | HG02027.hp2 NA19007.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.972-9418_972-9417d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94432476 | ||||||
| chr10:94432562 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-9334A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94432562 | |||||||
| chr10:94432574 | C | G | 1 | a0001c0002t0002g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.972-9322C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94432574 | |||||||
| chr10:94432781 | G | GT | 162 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.972-9104dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94432781 | ||||||
| chr10:94433017 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.972-8879C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433017 | |||||||
| chr10:94433040 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.972-8856A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433040 | |||||||
| chr10:94433081 | C | A | 1 | a0001c0001t0017g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.972-8815C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433081 | |||||||
| chr10:94433207 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-8689C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433207 | |||||||
| chr10:94433221 | C | T | 2 | a0001c0001t0006g0003 a0001c0001t0006g0009 |
2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.972-8675C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433221 | |||||||
| chr10:94433315 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-8581C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433315 | |||||||
| chr10:94433338 | C | T | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.972-8558C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433338 | |||||||
| chr10:94433349 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.972-8547C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433349 | |||||||
| chr10:94433644 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-8252C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433644 | |||||||
| chr10:94433686 | G | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.972-8210G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433686 | |||||||
| chr10:94433719 | G | A | 16 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.972-8177G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433719 | |||||||
| chr10:94433752 | A | G | 78 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.972-8144A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433752 | |||||||
| chr10:94433837 | C | T | 1 | a0001c0002t0003g0303 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.972-8059C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433837 | |||||||
| chr10:94433861 | A | G | 1 | a0001c0001t0011g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.972-8035A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433861 | |||||||
| chr10:94433920 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.972-7976T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433920 | |||||||
| chr10:94434129 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18950.hp2 NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.972-7767G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434129 | |||||||
| chr10:94434216 | T | C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-7680T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434216 | |||||||
| chr10:94434365 | G | T | 78 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.972-7531G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434365 | |||||||
| chr10:94434431 | G | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-7465G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434431 | |||||||
| chr10:94434433 | G | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.972-7463G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434433 | |||||||
| chr10:94434437 | T | C | 214 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.972-7459T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434437 | |||||||
| chr10:94434504 | TA | T | 15 | a0001c0001t0001g0017 a0001c0001t0005g0200 a0001c0001t0005g0201 others(12): Show |
15 | HG01515.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.972-7376delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94434504 | ||||||
| chr10:94434533 | C | A | 1 | a0001c0001t0005g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.972-7363C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434533 | |||||||
| chr10:94434670 | C | G | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-7226C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434670 | |||||||
| chr10:94434861 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.972-7035T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434861 | |||||||
| chr10:94435142 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.972-6754T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94435142 | |||||||
| chr10:94435310 | CAA | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-6584_972-6583d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94435310 | ||||||
| chr10:94435569 | G | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-6327G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94435569 | |||||||
| chr10:94435663 | G | A | 1 | a0001c0002t0002g0335 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.972-6233G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94435663 | |||||||
| chr10:94435990 | TTTATTCT others(7): Show |
T | 1 | a0001c0002t0003g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.972-5903_972-5890d others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94435990 | ||||||
| chr10:94436144 | CT | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0341 others(15): Show |
19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.972-5740delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94436144 | ||||||
| chr10:94436236 | G | C | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.972-5660G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436236 | |||||||
| chr10:94436530 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.972-5366A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436530 | |||||||
| chr10:94436649 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.972-5247T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436649 | |||||||
| chr10:94436675 | GA | G | 4 | a0001c0002t0002g0259 a0001c0002t0002g0278 a0001c0002t0002g0287 others(1): Show |
4 | HG02129.hp1 HG02523.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-5220delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436675 | |||||||
| chr10:94436691 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.972-5205C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436691 | |||||||
| chr10:94436711 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0139 |
2 | NA19005.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.972-5185A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436711 | |||||||
| chr10:94436794 | C | CT | 17 | a0001c0001t0001g0109 a0001c0001t0001g0152 a0001c0001t0001g0341 others(14): Show |
18 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-5090dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94436794 | ||||||
| chr10:94436879 | T | C | 1 | a0001c0002t0003g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.972-5017T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436879 | |||||||
| chr10:94436896 | C | T | 3 | a0001c0001t0001g0100 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02922.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-5000C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436896 | |||||||
| chr10:94436941 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-4955C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436941 | |||||||
| chr10:94436966 | A | G | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.972-4930A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436966 | |||||||
| chr10:94437059 | A | AT | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.972-4826dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437059 | ||||||
| chr10:94437332 | C | CTT | 16 | a0001c0001t0001g0152 a0001c0001t0001g0341 a0001c0001t0001g0342 others(13): Show |
17 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.972-4554_972-4553d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437332 | ||||||
| chr10:94437428 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-4468C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437428 | |||||||
| chr10:94437443 | A | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-4453A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437443 | |||||||
| chr10:94437569 | A | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.972-4327A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437569 | |||||||
| chr10:94437571 | T | C | 17 | a0001c0001t0001g0152 a0001c0001t0001g0341 a0001c0001t0001g0342 others(14): Show |
18 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-4325T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437571 | |||||||
| chr10:94437656 | C | T | 16 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.972-4240C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437656 | |||||||
| chr10:94437673 | G | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-4223G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437673 | |||||||
| chr10:94437772 | T | G | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-4124T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437772 | |||||||
| chr10:94437781 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.972-4115C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437781 | |||||||
| chr10:94437876 | A | G | 13 | a0001c0001t0001g0152 a0001c0001t0004g0001 a0001c0001t0004g0213 others(10): Show |
14 | HG02071.hp2 HG03225.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.972-4020A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437876 | |||||||
| chr10:94437957 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.972-3939T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437957 | |||||||
| chr10:94437991 | CT | C | 82 | a0001c0001t0001g0059 a0001c0001t0001g0186 a0001c0001t0001g0187 others(79): Show |
82 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.972-3878delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | ||||||
| chr10:94437991 | CTT | C | 84 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0044 others(81): Show |
85 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(82): Show |
intron_variant | MODIFIER | c.972-3879_972-3878d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | ||||||
| chr10:94437991 | CTTT | C | 148 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.972-3880_972-3878d others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | ||||||
| chr10:94437991 | CTTTT | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0079 others(5): Show |
8 | HG01928.hp1 HG02027.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.972-3881_972-3878d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | ||||||
| chr10:94438374 | T | A | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.972-3522T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438374 | |||||||
| chr10:94438424 | T | TA | 224 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.972-3470dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94438424 | ||||||
| chr10:94438451 | T | C | 12 | a0001c0001t0001g0152 a0001c0001t0004g0001 a0001c0001t0004g0213 others(9): Show |
13 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.972-3445T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438451 | |||||||
| chr10:94438539 | T | C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.972-3357T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438539 | |||||||
| chr10:94438765 | A | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-3131A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438765 | |||||||
| chr10:94438889 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-3007C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438889 | |||||||
| chr10:94438912 | A | T | 198 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.972-2984A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438912 | |||||||
| chr10:94438952 | C | T | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972-2944C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438952 | |||||||
| chr10:94439023 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | HG02155.hp1 NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.972-2873C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439023 | |||||||
| chr10:94439025 | A | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG00099.hp1 HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.972-2871A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439025 | |||||||
| chr10:94439117 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.972-2779C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439117 | |||||||
| chr10:94439337 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-2559A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439337 | |||||||
| chr10:94439475 | A | T | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.972-2421A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439475 | |||||||
| chr10:94439478 | T | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-2418T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439478 | |||||||
| chr10:94439614 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.972-2282C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439614 | |||||||
| chr10:94439778 | G | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-2118G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439778 | |||||||
| chr10:94439913 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.972-1983A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439913 | |||||||
| chr10:94440013 | G | T | 339 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.972-1883G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440013 | |||||||
| chr10:94440046 | A | G | 1 | a0001c0001t0011g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.972-1850A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440046 | |||||||
| chr10:94440063 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-1833G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440063 | |||||||
| chr10:94440164 | C | T | 187 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.972-1732C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440164 | |||||||
| chr10:94440343 | T | A | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.972-1553T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440343 | |||||||
| chr10:94440507 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.972-1389T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440507 | |||||||
| chr10:94440590 | C | T | 4 | a0001c0002t0002g0275 a0001c0002t0002g0276 a0001c0002t0002g0290 others(1): Show |
4 | NA18953.hp2 NA18970.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-1306C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440590 | |||||||
| chr10:94440798 | A | G | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.972-1098A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440798 | |||||||
| chr10:94440877 | GT | G | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-1018delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440877 | |||||||
| chr10:94440978 | T | A | 69 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(66): Show |
69 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.972-918T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440978 | |||||||
| chr10:94441000 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-896C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441000 | |||||||
| chr10:94441007 | G | A | 3 | a0001c0004t0012g0211 a0001c0004t0012g0212 a0002c0006t0013g0344 |
3 | HG02257.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.972-889G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441007 | |||||||
| chr10:94441039 | A | G | 224 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.972-857A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441039 | |||||||
| chr10:94441083 | C | T | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-813C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441083 | |||||||
| chr10:94441179 | A | T | 3 | a0001c0001t0001g0152 a0001c0001t0004g0001 a0001c0001t0004g0219 |
4 | NA18948.hp1 NA18979.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-717A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441179 | |||||||
| chr10:94441189 | A | G | 7 | a0001c0001t0001g0093 a0001c0001t0001g0150 a0001c0001t0001g0154 others(4): Show |
7 | HG00673.hp2 HG02083.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-707A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441189 | |||||||
| chr10:94441212 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.972-684G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441212 | |||||||
| chr10:94441251 | A | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-645A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441251 | |||||||
| chr10:94441292 | T | G | 1 | a0001c0002t0003g0305 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.972-604T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441292 | |||||||
| chr10:94441523 | T | C | 6 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 others(3): Show |
6 | HG02257.hp2 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-373T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441523 | |||||||
| chr10:94441858 | A | G | 17 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(14): Show |
17 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.972-38A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441858 | |||||||
| chr10:94442063 | C | T | 43 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(40): Show |
43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1095+44C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442063 | |||||||
| chr10:94442082 | CT | C | 70 | a0001c0001t0001g0189 a0001c0001t0002g0223 a0001c0001t0002g0239 others(67): Show |
70 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1095+80delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442082 | ||||||
| chr10:94442082 | CTT | C | 80 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0077 others(77): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1095+79_1095+80del others(2): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442082 | ||||||
| chr10:94442082 | CTTT | C | 81 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(78): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1095+78_1095+80del others(3): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442082 | ||||||
| chr10:94442085 | T | C | 19 | a0001c0001t0001g0152 a0001c0001t0002g0002 a0001c0001t0002g0224 others(16): Show |
21 | HG00642.hp1 HG01099.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1095+66T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442085 | |||||||
| chr10:94442086 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0239 |
2 | HG01167.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1095+67T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442086 | |||||||
| chr10:94442552 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1095+533A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442552 | |||||||
| chr10:94442645 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1095+626T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442645 | |||||||
| chr10:94442653 | A | G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+634A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442653 | |||||||
| chr10:94442718 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1095+699T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442718 | |||||||
| chr10:94442928 | C | T | 1 | a0001c0002t0002g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1095+909C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442928 | |||||||
| chr10:94442945 | CT | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+933delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442945 | ||||||
| chr10:94443023 | G | A | 3 | a0001c0002t0002g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 |
3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1095+1004G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443023 | |||||||
| chr10:94443136 | C | T | 2 | a0001c0002t0002g0225 a0001c0002t0002g0226 |
2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1095+1117C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443136 | |||||||
| chr10:94443138 | C | T | 2 | a0001c0002t0002g0225 a0001c0002t0002g0226 |
2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1095+1119C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443138 | |||||||
| chr10:94443186 | CAG | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0342 others(1): Show |
4 | HG00639.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+1169_1095+117 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94443186 | ||||||
| chr10:94443298 | C | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+1279C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443298 | |||||||
| chr10:94443886 | G | A | 15 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(12): Show |
15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+1867G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443886 | |||||||
| chr10:94443907 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1095+1888C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443907 | |||||||
| chr10:94444124 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0083 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1095+2105C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444124 | |||||||
| chr10:94444172 | GA | G | 7 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095+2168delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94444172 | ||||||
| chr10:94444190 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+2171A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444190 | |||||||
| chr10:94444227 | A | AT | 8 | a0001c0001t0001g0100 a0001c0001t0001g0196 a0001c0001t0002g0223 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1095+2220dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94444227 | ||||||
| chr10:94444357 | G | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+2338G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444357 | |||||||
| chr10:94444462 | C | T | 13 | a0001c0002t0003g0304 a0001c0002t0003g0305 a0001c0002t0003g0309 others(10): Show |
13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+2443C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444462 | |||||||
| chr10:94444733 | CT | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0071 a0001c0001t0001g0085 others(7): Show |
10 | HG01517.hp1 HG02083.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+2730delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94444733 | ||||||
| chr10:94444771 | G | A | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1095+2752G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444771 | |||||||
| chr10:94444988 | T | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1095+2969T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444988 | |||||||
| chr10:94445136 | A | G | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1095+3117A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445136 | |||||||
| chr10:94445164 | T | C | 5 | a0001c0001t0001g0100 a0001c0001t0002g0231 a0001c0003t0008g0012 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+3145T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445164 | |||||||
| chr10:94445206 | A | C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+3187A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445206 | |||||||
| chr10:94445215 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+3196T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445215 | |||||||
| chr10:94445337 | A | G | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1095+3318A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445337 | |||||||
| chr10:94445470 | C | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+3451C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445470 | |||||||
| chr10:94445558 | A | G | 5 | a0001c0001t0001g0100 a0001c0001t0002g0231 a0001c0003t0008g0012 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+3539A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445558 | |||||||
| chr10:94445812 | G | A | 2 | a0001c0002t0003g0302 a0001c0002t0003g0303 |
2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1095+3793G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445812 | |||||||
| chr10:94445845 | G | A | 1 | a0001c0001t0005g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1095+3826G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445845 | |||||||
| chr10:94445887 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1095+3868G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445887 | |||||||
| chr10:94446272 | A | T | 1 | a0001c0001t0005g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1095+4253A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446272 | |||||||
| chr10:94446288 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1095+4269T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446288 | |||||||
| chr10:94446347 | T | G | 196 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1095+4328T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446347 | |||||||
| chr10:94446352 | A | G | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1095+4333A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446352 | |||||||
| chr10:94446440 | G | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1095+4421G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446440 | |||||||
| chr10:94446563 | AT | A | 41 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(38): Show |
41 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1095+4553delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94446563 | ||||||
| chr10:94446575 | A | G | 215 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1095+4556A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446575 | |||||||
| chr10:94446626 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+4607G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446626 | |||||||
| chr10:94446850 | G | A | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1095+4831G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446850 | |||||||
| chr10:94446936 | A | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1095+4917A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446936 | |||||||
| chr10:94447005 | A | G | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+4986A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447005 | |||||||
| chr10:94447024 | G | C | 2 | a0001c0002t0003g0304 a0001c0002t0003g0310 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1095+5005G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447024 | |||||||
| chr10:94447045 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1095+5026C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447045 | |||||||
| chr10:94447057 | C | CA | 142 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(139): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1095+5057dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447057 | ||||||
| chr10:94447057 | C | CAA | 25 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0040 others(22): Show |
25 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1095+5056_1095+505 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447057 | ||||||
| chr10:94447057 | CA | C | 17 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(14): Show |
17 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1095+5057delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447057 | ||||||
| chr10:94447070 | A | C | 1 | a0001c0002t0002g0267 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1095+5051A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447070 | |||||||
| chr10:94447072 | A | C | 1 | a0001c0001t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1095+5053A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447072 | |||||||
| chr10:94447111 | C | T | 15 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(12): Show |
15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+5092C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447111 | |||||||
| chr10:94447223 | G | A | 1 | a0001c0001t0004g0222 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1095+5204G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447223 | |||||||
| chr10:94447235 | A | G | 195 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1095+5216A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447235 | |||||||
| chr10:94447265 | T | C | 4 | a0001c0002t0002g0275 a0001c0002t0002g0276 a0001c0002t0002g0290 others(1): Show |
4 | NA18953.hp2 NA18970.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+5246T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447265 | |||||||
| chr10:94447335 | C | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1095+5316C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447335 | |||||||
| chr10:94447691 | A | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+5672A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447691 | |||||||
| chr10:94447751 | G | GT | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+5741dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447751 | ||||||
| chr10:94447779 | T | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+5760T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447779 | |||||||
| chr10:94447803 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1095+5784T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447803 | |||||||
| chr10:94447846 | T | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+5827T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447846 | |||||||
| chr10:94448025 | A | C | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1095+6006A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448025 | |||||||
| chr10:94448377 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+6358A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448377 | |||||||
| chr10:94448588 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+6569C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448588 | |||||||
| chr10:94448694 | G | A | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1095+6675G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448694 | |||||||
| chr10:94448717 | T | G | 201 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(198): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1095+6698T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448717 | |||||||
| chr10:94448863 | T | A | 1 | a0001c0002t0003g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1095+6844T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448863 | |||||||
| chr10:94448886 | G | A | 1 | a0001c0002t0003g0308 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1095+6867G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448886 | |||||||
| chr10:94449011 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1095+6992T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449011 | |||||||
| chr10:94449058 | T | C | 1 | a0001c0002t0002g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1095+7039T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449058 | |||||||
| chr10:94449102 | C | T | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1095+7083C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449102 | |||||||
| chr10:94449103 | G | A | 2 | a0001c0002t0003g0230 a0001c0002t0003g0324 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1095+7084G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449103 | |||||||
| chr10:94449336 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+7317C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449336 | |||||||
| chr10:94449479 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1095+7460A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449479 | |||||||
| chr10:94449480 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1095+7461C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449480 | |||||||
| chr10:94449491 | C | T | 2 | a0001c0002t0003g0178 a0001c0002t0003g0179 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1095+7472C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449491 | |||||||
| chr10:94449549 | G | T | 16 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(13): Show |
17 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1095+7530G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449549 | |||||||
| chr10:94449687 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+7668G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449687 | |||||||
| chr10:94449708 | T | C | 1 | a0001c0002t0003g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1095+7689T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449708 | |||||||
| chr10:94449854 | T | G | 1 | a0001c0002t0002g0289 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1095+7835T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449854 | |||||||
| chr10:94449911 | A | G | 215 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1095+7892A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449911 | |||||||
| chr10:94450121 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00423.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1095+8102A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450121 | |||||||
| chr10:94450309 | G | A | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1095+8290G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450309 | |||||||
| chr10:94450480 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1095+8461A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450480 | |||||||
| chr10:94450608 | G | C | 16 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(13): Show |
17 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1095+8589G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450608 | |||||||
| chr10:94450627 | G | C | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+8608G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450627 | |||||||
| chr10:94450643 | G | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1095+8624G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450643 | |||||||
| chr10:94450714 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+8695A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450714 | |||||||
| chr10:94451110 | T | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+9091T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451110 | |||||||
| chr10:94451151 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+9132T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451151 | |||||||
| chr10:94451542 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+9523G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451542 | |||||||
| chr10:94451638 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+9619A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451638 | |||||||
| chr10:94451708 | G | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+9689G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451708 | |||||||
| chr10:94451757 | A | G | 215 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1095+9738A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451757 | |||||||
| chr10:94452072 | GCATATAT others(23): Show |
G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+10083_1095+10 others(36): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94452072 | ||||||
| chr10:94452102 | T | G | 18 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(15): Show |
19 | HG01884.hp2 HG02071.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095+10083T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452102 | |||||||
| chr10:94452192 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1095+10173A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452192 | |||||||
| chr10:94452216 | C | T | 2 | a0001c0002t0003g0308 a0001c0002t0003g0317 |
2 | HG02015.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1095+10197C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452216 | |||||||
| chr10:94452251 | G | A | 2 | a0001c0002t0003g0311 a0001c0002t0003g0312 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1095+10232G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452251 | |||||||
| chr10:94452344 | T | G | 1 | a0001c0002t0002g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1095+10325T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452344 | |||||||
| chr10:94452470 | A | G | 5 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0261 others(2): Show |
5 | HG00735.hp2 HG00741.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095+10451A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452470 | |||||||
| chr10:94452548 | T | G | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+10529T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452548 | |||||||
| chr10:94452979 | T | C | 5 | a0001c0001t0001g0100 a0001c0001t0002g0231 a0001c0003t0008g0012 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+10960T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452979 | |||||||
| chr10:94453177 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+11158C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453177 | |||||||
| chr10:94453253 | G | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+11234G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453253 | |||||||
| chr10:94453339 | C | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0086 others(1): Show |
4 | HG02040.hp2 NA18983.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+11320C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453339 | |||||||
| chr10:94453802 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1095+11783G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453802 | |||||||
| chr10:94453827 | TC | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+11809delC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453827 | |||||||
| chr10:94454129 | T | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+12110T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454129 | |||||||
| chr10:94454224 | GTCT | G | 10 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
10 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+12210_1095+12 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94454224 | ||||||
| chr10:94454462 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1095+12443C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454462 | |||||||
| chr10:94454747 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1095+12728T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454747 | |||||||
| chr10:94454806 | A | G | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1095+12787A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454806 | |||||||
| chr10:94454914 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1095+12895T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454914 | |||||||
| chr10:94454935 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+12916G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454935 | |||||||
| chr10:94454966 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1095+12947A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454966 | |||||||
| chr10:94455024 | A | G | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1095+13005A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455024 | |||||||
| chr10:94455188 | A | AT | 7 | a0001c0001t0001g0192 a0001c0001t0001g0341 a0001c0001t0001g0342 others(4): Show |
7 | HG00323.hp2 HG01261.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1095+13181dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94455188 | ||||||
| chr10:94455295 | T | C | 12 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+13276T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455295 | |||||||
| chr10:94455318 | A | C | 156 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1095+13299A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455318 | |||||||
| chr10:94455483 | G | A | 49 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(46): Show |
49 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1095+13464G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455483 | |||||||
| chr10:94455540 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+13521T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455540 | |||||||
| chr10:94455624 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+13605A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455624 | |||||||
| chr10:94455670 | C | T | 1 | a0001c0002t0003g0312 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1095+13651C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455670 | |||||||
| chr10:94455963 | A | AG | 4 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0086 others(1): Show |
4 | HG02040.hp2 NA18983.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+13945dupG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94455963 | ||||||
| chr10:94456037 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1095+14018T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94456037 | |||||||
| chr10:94456462 | A | C | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+14443A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94456462 | |||||||
| chr10:94456899 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1095+14880C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94456899 | |||||||
| chr10:94457039 | A | G | 1 | a0001c0001t0005g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1095+15020A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457039 | |||||||
| chr10:94457310 | T | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+15291T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457310 | |||||||
| chr10:94457330 | T | TA | 4 | a0001c0001t0001g0100 a0001c0003t0008g0012 a0001c0003t0008g0013 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+15314dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94457330 | ||||||
| chr10:94457382 | A | G | 1 | a0001c0001t0014g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1095+15363A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457382 | |||||||
| chr10:94457460 | G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+15441G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457460 | |||||||
| chr10:94457474 | G | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+15455G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457474 | |||||||
| chr10:94457477 | T | C | 270 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1095+15458T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457477 | |||||||
| chr10:94457636 | C | T | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+15617C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457636 | |||||||
| chr10:94458107 | C | T | 65 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(62): Show |
65 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1095+16088C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458107 | |||||||
| chr10:94458152 | A | G | 47 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(44): Show |
47 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.1095+16133A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458152 | |||||||
| chr10:94458287 | C | T | 3 | a0001c0001t0001g0100 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02922.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1095+16268C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458287 | |||||||
| chr10:94458289 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(1): Show |
4 | HG02698.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+16270C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458289 | |||||||
| chr10:94458336 | A | G | 2 | a0001c0001t0006g0004 a0001c0001t0026g0006 |
2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1095+16317A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458336 | |||||||
| chr10:94458381 | C | T | 215 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1096-16287C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458381 | |||||||
| chr10:94458503 | C | T | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1096-16165C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458503 | |||||||
| chr10:94458592 | C | T | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1096-16076C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458592 | |||||||
| chr10:94458622 | T | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-16046T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458622 | |||||||
| chr10:94458720 | C | G | 164 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1096-15948C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458720 | |||||||
| chr10:94458741 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1096-15927C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458741 | |||||||
| chr10:94458785 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0026g0006 |
2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1096-15883G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458785 | |||||||
| chr10:94458793 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-15875C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458793 | |||||||
| chr10:94458797 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1096-15871C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458797 | |||||||
| chr10:94458817 | G | A | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-15851G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458817 | |||||||
| chr10:94458877 | G | T | 11 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-15791G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458877 | |||||||
| chr10:94458953 | A | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096-15715A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458953 | |||||||
| chr10:94458970 | G | A | 7 | a0001c0002t0002g0236 a0001c0002t0002g0246 a0001c0002t0002g0247 others(4): Show |
7 | HG00408.hp2 HG01515.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-15698G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458970 | |||||||
| chr10:94458996 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1096-15672G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458996 | |||||||
| chr10:94459022 | A | C | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1096-15646A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459022 | |||||||
| chr10:94459208 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-15460A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459208 | |||||||
| chr10:94459227 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-15441A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459227 | |||||||
| chr10:94459430 | C | T | 15 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(12): Show |
15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-15238C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459430 | |||||||
| chr10:94459458 | G | T | 1 | a0001c0011t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1096-15210G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459458 | |||||||
| chr10:94459478 | A | AC | 7 | a0001c0001t0001g0111 a0001c0001t0005g0206 a0001c0002t0002g0290 others(4): Show |
7 | HG01175.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-15188dupC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94459478 | ||||||
| chr10:94459493 | C | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-15175C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459493 | |||||||
| chr10:94459494 | G | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-15174G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459494 | |||||||
| chr10:94459548 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | HG02129.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1096-15120G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459548 | |||||||
| chr10:94459592 | G | C | 2 | a0001c0001t0002g0268 a0001c0001t0002g0279 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1096-15076G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459592 | |||||||
| chr10:94459643 | G | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-15025G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459643 | |||||||
| chr10:94459689 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-14979C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459689 | |||||||
| chr10:94459768 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1096-14900A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459768 | |||||||
| chr10:94459888 | C | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1096-14780C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459888 | |||||||
| chr10:94459979 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1096-14689C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459979 | |||||||
| chr10:94460087 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-14581C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460087 | |||||||
| chr10:94460106 | C | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0094 |
2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1096-14562C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460106 | |||||||
| chr10:94460187 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0094 |
2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1096-14481A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460187 | |||||||
| chr10:94460216 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1096-14452G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460216 | |||||||
| chr10:94460343 | A | G | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1096-14325A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460343 | |||||||
| chr10:94460395 | A | G | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-14273A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460395 | |||||||
| chr10:94460404 | A | G | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1096-14264A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460404 | |||||||
| chr10:94460404 | AT | A | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1096-14256delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94460404 | ||||||
| chr10:94460560 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1096-14108G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460560 | |||||||
| chr10:94460636 | G | A | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-14032G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460636 | |||||||
| chr10:94460731 | C | T | 1 | a0001c0002t0002g0257 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1096-13937C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460731 | |||||||
| chr10:94460777 | C | T | 1 | a0001c0002t0003g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1096-13891C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460777 | |||||||
| chr10:94460858 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-13810C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460858 | |||||||
| chr10:94461179 | A | T | 15 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(12): Show |
15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-13489A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461179 | |||||||
| chr10:94461333 | C | T | 3 | a0001c0002t0002g0327 a0001c0002t0002g0328 a0001c0002t0002g0329 |
3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1096-13335C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461333 | |||||||
| chr10:94461671 | C | T | 1 | a0001c0002t0016g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1096-12997C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461671 | |||||||
| chr10:94461728 | C | CA | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1096-12939dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94461728 | ||||||
| chr10:94461970 | C | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1096-12698C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461970 | |||||||
| chr10:94462022 | T | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1096-12646T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462022 | |||||||
| chr10:94462078 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1096-12590A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462078 | |||||||
| chr10:94462097 | G | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-12571G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462097 | |||||||
| chr10:94462357 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1096-12311G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462357 | |||||||
| chr10:94462533 | T | C | 1 | a0001c0002t0002g0328 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1096-12135T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462533 | |||||||
| chr10:94462691 | AATT | A | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-11973_1096-11 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94462691 | ||||||
| chr10:94463084 | T | A | 157 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1096-11584T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463084 | |||||||
| chr10:94463398 | C | T | 2 | a0001c0001t0004g0214 a0001c0001t0004g0218 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1096-11270C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463398 | |||||||
| chr10:94463510 | T | A | 157 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1096-11158T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463510 | |||||||
| chr10:94463649 | A | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-11019A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463649 | |||||||
| chr10:94463956 | G | A | 1 | a0001c0001t0014g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1096-10712G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463956 | |||||||
| chr10:94464093 | T | C | 2 | a0001c0001t0005g0200 a0001c0001t0005g0206 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1096-10575T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464093 | |||||||
| chr10:94464150 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-10518G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464150 | |||||||
| chr10:94464298 | C | CTGGTCTT others(313): Show |
1 | a0001c0002t0002g0252 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1096-10350_1096-10 others(326): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94464298 | ||||||
| chr10:94464581 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-10087T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464581 | |||||||
| chr10:94464637 | A | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-10031A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464637 | |||||||
| chr10:94464913 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1096-9755G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464913 | |||||||
| chr10:94464921 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1096-9747T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464921 | |||||||
| chr10:94465438 | G | A | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-9230G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465438 | |||||||
| chr10:94465517 | G | A | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1096-9151G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465517 | |||||||
| chr10:94465519 | G | A | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-9149G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465519 | |||||||
| chr10:94465538 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0138 |
2 | NA19007.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1096-9130C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465538 | |||||||
| chr10:94465560 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-9108C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465560 | |||||||
| chr10:94465602 | TGCCACTG others(7): Show |
T | 2 | a0001c0001t0005g0200 a0001c0001t0005g0206 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1096-9062_1096-904 others(18): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465602 | ||||||
| chr10:94465635 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | HG02129.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1096-9033G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465635 | |||||||
| chr10:94465653 | A | AT | 6 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0203 others(3): Show |
6 | HG02723.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-9015_1096-901 others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465653 | |||||||
| chr10:94465653 | A | ATAT | 4 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-9015_1096-901 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465653 | |||||||
| chr10:94465655 | A | AAAT | 11 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0124 others(8): Show |
11 | HG00639.hp2 HG01123.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-9012_1096-901 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465655 | ||||||
| chr10:94465655 | A | AAT | 52 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(49): Show |
53 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.1096-8998_1096-899 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465655 | ||||||
| chr10:94465655 | A | AATATAT | 9 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0215 others(6): Show |
10 | HG04204.hp2 NA18948.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096-9002_1096-899 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465655 | ||||||
| chr10:94465655 | A | T | 14 | a0001c0001t0001g0186 a0001c0001t0002g0231 a0001c0001t0005g0200 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-9013A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465655 | |||||||
| chr10:94465657 | T | A | 146 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1096-9011T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465657 | |||||||
| chr10:94465659 | T | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0134 a0001c0001t0001g0138 |
3 | HG02074.hp1 NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1096-9009T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465659 | |||||||
| chr10:94465668 | A | G | 7 | a0001c0001t0005g0203 a0001c0001t0005g0205 a0001c0001t0005g0207 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-9000A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465668 | |||||||
| chr10:94465670 | A | ATATGTG | 4 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0082 others(1): Show |
4 | HG00099.hp1 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATATGTGT others(1): Show |
71 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATATGTGT others(3): Show |
64 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATATGTGT others(5): Show |
5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0107 others(2): Show |
5 | HG01257.hp1 HG02040.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATG | 4 | a0001c0001t0001g0191 a0001c0001t0002g0025 a0001c0002t0003g0317 others(1): Show |
4 | HG02015.hp2 HG02486.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-8972_1096-897 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATGTG | 12 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0187 others(9): Show |
12 | HG01891.hp1 HG02080.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096-8974_1096-897 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATGTGTG | 10 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0083 others(7): Show |
10 | HG02257.hp1 HG02602.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-8976_1096-897 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0095 a0001c0001t0001g0115 a0001c0001t0001g0121 others(6): Show |
9 | HG00639.hp2 HG01123.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096-8978_1096-897 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0166 |
3 | HG00673.hp2 HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1096-8980_1096-897 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465670 | A | G | 20 | a0001c0001t0001g0186 a0001c0001t0002g0231 a0001c0001t0005g0201 others(17): Show |
20 | HG02129.hp1 HG02145.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1096-8998A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465670 | |||||||
| chr10:94465670 | ATGTGTG | A | 8 | a0001c0002t0002g0248 a0001c0002t0002g0284 a0001c0002t0002g0294 others(5): Show |
8 | HG00323.hp2 HG01069.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-8976_1096-897 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | ||||||
| chr10:94465672 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0109 |
2 | HG00597.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1096-8996G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465672 | |||||||
| chr10:94465678 | G | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-8990G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465678 | |||||||
| chr10:94465680 | G | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-8988G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465680 | |||||||
| chr10:94465694 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8974G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465694 | |||||||
| chr10:94465695 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8973T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465695 | |||||||
| chr10:94465696 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8972G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465696 | |||||||
| chr10:94465699 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8969C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465699 | |||||||
| chr10:94465702 | A | ATATACG | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1096-8954_1096-894 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465702 | ||||||
| chr10:94465715 | TATAC | T | 164 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1096-8936_1096-893 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465715 | ||||||
| chr10:94465732 | A | G | 2 | a0001c0003t0008g0013 a0001c0003t0008g0014 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1096-8936A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465732 | |||||||
| chr10:94465735 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-8933C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465735 | |||||||
| chr10:94465746 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-8922A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465746 | |||||||
| chr10:94465753 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0172 |
2 | HG02129.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1096-8915T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465753 | |||||||
| chr10:94465768 | GTATACGC others(13): Show |
G | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1096-8881_1096-886 others(24): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465768 | ||||||
| chr10:94465773 | C | T | 10 | a0001c0001t0001g0097 a0001c0001t0002g0002 a0001c0001t0002g0223 others(7): Show |
11 | HG00597.hp2 HG00642.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-8895C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465773 | |||||||
| chr10:94465787 | C | T | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8881C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465787 | |||||||
| chr10:94465789 | T | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8879T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465789 | |||||||
| chr10:94465790 | A | G | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8878A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465790 | |||||||
| chr10:94465791 | T | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8877T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465791 | |||||||
| chr10:94465793 | C | CACAT | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-8875_1096-887 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465793 | |||||||
| chr10:94465793 | C | T | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8875C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465793 | |||||||
| chr10:94465794 | G | A | 168 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1096-8874G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465794 | |||||||
| chr10:94465794 | G | GCATA | 16 | a0001c0001t0002g0231 a0001c0001t0005g0200 a0001c0001t0005g0201 others(13): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1096-8865_1096-886 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465794 | ||||||
| chr10:94465794 | G | GCATACAT others(1): Show |
11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1096-8869_1096-886 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465794 | ||||||
| chr10:94465807 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1096-8861T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465807 | |||||||
| chr10:94465876 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-8792A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465876 | |||||||
| chr10:94465895 | C | T | 267 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1096-8773C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465895 | |||||||
| chr10:94465902 | A | G | 2 | a0001c0001t0002g0273 a0002c0006t0013g0344 |
2 | HG01978.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1096-8766A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465902 | |||||||
| chr10:94465920 | A | G | 1 | a0001c0002t0002g0333 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1096-8748A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465920 | |||||||
| chr10:94465943 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-8725C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465943 | |||||||
| chr10:94465946 | G | A | 188 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1096-8722G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465946 | |||||||
| chr10:94466136 | TTGTAAGA others(8): Show |
T | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1096-8517_1096-850 others(19): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94466136 | ||||||
| chr10:94466454 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-8214A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466454 | |||||||
| chr10:94466495 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0019g0020 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1096-8173T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466495 | |||||||
| chr10:94466679 | G | T | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1096-7989G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466679 | |||||||
| chr10:94466693 | C | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-7975C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466693 | |||||||
| chr10:94466751 | A | T | 1 | a0001c0002t0009g0334 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1096-7917A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466751 | |||||||
| chr10:94467225 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1096-7443T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467225 | |||||||
| chr10:94467243 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1096-7425G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467243 | |||||||
| chr10:94467293 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1096-7375C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467293 | |||||||
| chr10:94467341 | T | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-7327T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467341 | |||||||
| chr10:94467376 | G | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-7292G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467376 | |||||||
| chr10:94467395 | G | A | 1 | a0001c0002t0002g0275 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1096-7273G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467395 | |||||||
| chr10:94467651 | C | A | 6 | a0001c0002t0002g0248 a0001c0002t0002g0284 a0001c0002t0002g0294 others(3): Show |
6 | HG00323.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1096-7017C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467651 | |||||||
| chr10:94467655 | C | CT | 168 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1096-7005dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94467655 | ||||||
| chr10:94467673 | A | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1096-6995A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467673 | |||||||
| chr10:94467814 | C | T | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-6854C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467814 | |||||||
| chr10:94468127 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1096-6541A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468127 | |||||||
| chr10:94468532 | A | G | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1096-6136A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468532 | |||||||
| chr10:94468746 | G | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-5922G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468746 | |||||||
| chr10:94468768 | G | T | 1 | a0001c0002t0022g0296 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1096-5900G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468768 | |||||||
| chr10:94468880 | G | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0241 |
3 | HG01516.hp2 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1096-5788G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468880 | |||||||
| chr10:94469017 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1096-5651T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469017 | |||||||
| chr10:94469020 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-5648T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469020 | |||||||
| chr10:94469098 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-5570A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469098 | |||||||
| chr10:94469409 | C | T | 259 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1096-5259C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469409 | |||||||
| chr10:94469429 | A | G | 339 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1096-5239A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469429 | |||||||
| chr10:94469447 | C | CT | 95 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(92): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1096-5202dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94469447 | ||||||
| chr10:94469447 | C | CTT | 10 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0110 others(7): Show |
10 | HG02015.hp1 HG02886.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-5203_1096-520 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94469447 | ||||||
| chr10:94469447 | C | CTTT | 70 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1096-5204_1096-520 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94469447 | ||||||
| chr10:94469447 | C | T | 1 | a0001c0001t0006g0009 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1096-5221C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469447 | |||||||
| chr10:94469762 | C | T | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1096-4906C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469762 | |||||||
| chr10:94469789 | T | A | 7 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-4879T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469789 | |||||||
| chr10:94469857 | T | C | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-4811T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469857 | |||||||
| chr10:94469869 | G | A | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-4799G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469869 | |||||||
| chr10:94470008 | T | C | 7 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-4660T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470008 | |||||||
| chr10:94470031 | G | T | 5 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-4637G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470031 | |||||||
| chr10:94470320 | A | G | 1 | a0001c0001t0006g0005 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1096-4348A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470320 | |||||||
| chr10:94470526 | G | A | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-4142G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470526 | |||||||
| chr10:94470593 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1096-4075G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470593 | |||||||
| chr10:94470595 | A | C | 2 | a0001c0002t0003g0304 a0001c0002t0003g0310 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1096-4073A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470595 | |||||||
| chr10:94470690 | C | CT | 34 | a0001c0001t0001g0057 a0001c0001t0001g0100 a0001c0001t0001g0108 others(31): Show |
34 | HG01074.hp2 HG01515.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1096-3958dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | ||||||
| chr10:94470690 | C | CTT | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-3959_1096-395 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | ||||||
| chr10:94470690 | CT | C | 40 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0066 others(37): Show |
40 | HG00642.hp2 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-3958delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | ||||||
| chr10:94470690 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0004g0221 a0001c0001t0004g0222 |
2 | NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1096-3967_1096-395 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | ||||||
| chr10:94470731 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0241 |
3 | HG01516.hp2 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1096-3937A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470731 | |||||||
| chr10:94470732 | G | A | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1096-3936G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470732 | |||||||
| chr10:94470743 | T | C | 9 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0237 others(6): Show |
9 | HG01928.hp2 HG02056.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096-3925T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470743 | |||||||
| chr10:94470796 | A | G | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1096-3872A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470796 | |||||||
| chr10:94470870 | TTTA | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-3788_1096-378 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470870 | ||||||
| chr10:94471088 | C | A | 2 | a0001c0002t0002g0262 a0001c0002t0002g0266 |
2 | HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1096-3580C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471088 | |||||||
| chr10:94471121 | C | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-3547C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471121 | |||||||
| chr10:94471156 | A | G | 1 | a0001c0002t0002g0286 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1096-3512A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471156 | |||||||
| chr10:94471278 | C | CA | 20 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0062 others(17): Show |
20 | HG00438.hp1 HG01175.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1096-3373dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94471278 | ||||||
| chr10:94471278 | CA | C | 10 | a0001c0001t0001g0114 a0001c0001t0001g0152 a0001c0001t0006g0003 others(7): Show |
10 | HG00099.hp2 HG01978.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-3373delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94471278 | ||||||
| chr10:94471300 | A | G | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-3368A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471300 | |||||||
| chr10:94471309 | G | C | 7 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-3359G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471309 | |||||||
| chr10:94471412 | G | A | 65 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1096-3256G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471412 | |||||||
| chr10:94471607 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1096-3061C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471607 | |||||||
| chr10:94471998 | T | A | 7 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-2670T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471998 | |||||||
| chr10:94473021 | G | GT | 4 | a0001c0001t0001g0100 a0001c0003t0008g0012 a0001c0003t0008g0013 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-1641dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473021 | ||||||
| chr10:94473129 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0136 a0001c0001t0001g0138 others(1): Show |
4 | HG02027.hp2 NA19004.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-1539C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473129 | |||||||
| chr10:94473137 | A | G | 3 | a0001c0002t0002g0228 a0001c0002t0002g0283 a0001c0002t0002g0285 |
3 | HG01981.hp2 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1096-1531A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473137 | |||||||
| chr10:94473198 | C | CA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG00423.hp2 HG00438.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-1457dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473198 | ||||||
| chr10:94473353 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0032 |
3 | HG00597.hp1 NA18612.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1096-1315T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473353 | |||||||
| chr10:94473382 | GA | G | 5 | a0001c0001t0002g0231 a0001c0002t0002g0225 a0001c0002t0002g0226 others(2): Show |
5 | HG02451.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-1276delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473382 | ||||||
| chr10:94473439 | T | C | 18 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(15): Show |
19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1096-1229T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473439 | |||||||
| chr10:94473853 | TATTAA | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-809_1096-805d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473853 | ||||||
| chr10:94473903 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1096-765G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473903 | |||||||
| chr10:94473914 | T | A | 18 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(15): Show |
19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1096-754T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473914 | |||||||
| chr10:94474128 | T | G | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-540T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474128 | |||||||
| chr10:94474239 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-429A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474239 | |||||||
| chr10:94474282 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096-386A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474282 | |||||||
| chr10:94474338 | CA | C | 327 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(324): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1096-319delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94474338 | ||||||
| chr10:94474526 | T | G | 2 | a0001c0001t0002g0280 a0001c0001t0002g0288 |
2 | HG01361.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1096-142T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474526 | |||||||
| chr10:94474930 | A | G | 1 | a0001c0001t0015g0092 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1211+147A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94474930 | |||||||
| chr10:94474980 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1211+197G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94474980 | |||||||
| chr10:94475141 | C | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1211+358C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475141 | |||||||
| chr10:94475343 | G | A | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1211+560G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475343 | |||||||
| chr10:94475370 | A | C | 1 | a0001c0002t0003g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1211+587A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475370 | |||||||
| chr10:94475485 | T | C | 18 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(15): Show |
19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1211+702T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475485 | |||||||
| chr10:94475628 | G | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1211+845G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475628 | |||||||
| chr10:94475671 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1211+888A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475671 | |||||||
| chr10:94475721 | C | T | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1211+938C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475721 | |||||||
| chr10:94475968 | C | T | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1211+1185C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475968 | |||||||
| chr10:94476111 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1211+1328T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476111 | |||||||
| chr10:94476341 | G | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1211+1558G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476341 | |||||||
| chr10:94476350 | A | G | 1 | a0001c0002t0002g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1211+1567A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476350 | |||||||
| chr10:94476383 | A | G | 168 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1211+1600A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476383 | |||||||
| chr10:94476412 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+1629C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476412 | |||||||
| chr10:94476434 | G | C | 47 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(44): Show |
47 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1211+1651G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476434 | |||||||
| chr10:94476483 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+1700C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476483 | |||||||
| chr10:94477245 | T | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02083.hp2 HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1211+2462T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94477245 | |||||||
| chr10:94477282 | CT | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0050 |
3 | HG02293.hp2 NA18939.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1211+2504delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94477282 | ||||||
| chr10:94477312 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1211+2529C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94477312 | |||||||
| chr10:94477652 | T | C | 16 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1211+2869T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94477652 | |||||||
| chr10:94478163 | T | A | 1 | a0001c0004t0012g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1211+3380T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478163 | |||||||
| chr10:94478189 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1211+3406G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478189 | |||||||
| chr10:94478567 | C | G | 195 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1211+3784C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478567 | |||||||
| chr10:94478628 | A | T | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1211+3845A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478628 | |||||||
| chr10:94478652 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1211+3869A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478652 | |||||||
| chr10:94478786 | A | C | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1211+4003A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478786 | |||||||
| chr10:94478846 | G | A | 1 | a0001c0002t0003g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1211+4063G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478846 | |||||||
| chr10:94478852 | G | A | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1211+4069G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478852 | |||||||
| chr10:94478880 | A | G | 197 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1211+4097A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478880 | |||||||
| chr10:94478930 | T | C | 1 | a0001c0002t0002g0333 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1211+4147T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478930 | |||||||
| chr10:94479216 | G | A | 4 | a0001c0002t0003g0302 a0001c0002t0003g0303 a0001c0002t0010g0306 others(1): Show |
4 | HG01192.hp1 HG02735.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+4433G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479216 | |||||||
| chr10:94479224 | C | G | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1211+4441C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479224 | |||||||
| chr10:94479326 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+4543C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479326 | |||||||
| chr10:94479569 | G | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1211+4786G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479569 | |||||||
| chr10:94479575 | A | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211+4792A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479575 | |||||||
| chr10:94479622 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | HG02129.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1211+4839G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479622 | |||||||
| chr10:94479671 | A | G | 1 | a0001c0002t0003g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1211+4888A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479671 | |||||||
| chr10:94479715 | T | A | 1 | a0001c0002t0002g0264 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1211+4932T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479715 | |||||||
| chr10:94479853 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+5070G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479853 | |||||||
| chr10:94479962 | G | C | 270 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1211+5179G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479962 | |||||||
| chr10:94479990 | T | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+5207T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479990 | |||||||
| chr10:94480461 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0151 |
2 | NA19000.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1211+5678A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480461 | |||||||
| chr10:94480685 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1211+5902C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480685 | |||||||
| chr10:94480695 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1211+5912A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480695 | |||||||
| chr10:94480697 | T | A | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1211+5914T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480697 | |||||||
| chr10:94480701 | T | C | 4 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+5918T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480701 | |||||||
| chr10:94480723 | T | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1211+5940T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480723 | |||||||
| chr10:94480781 | G | A | 1 | a0001c0001t0006g0010 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1211+5998G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480781 | |||||||
| chr10:94480865 | A | G | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1211+6082A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480865 | |||||||
| chr10:94481045 | C | CT | 45 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0131 others(42): Show |
45 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1211+6280dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94481045 | ||||||
| chr10:94481045 | CT | C | 27 | a0001c0001t0001g0100 a0001c0001t0001g0341 a0001c0001t0001g0342 others(24): Show |
27 | HG01169.hp2 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1211+6280delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94481045 | ||||||
| chr10:94481121 | T | C | 5 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0261 others(2): Show |
5 | HG00735.hp2 HG00741.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1211+6338T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481121 | |||||||
| chr10:94481249 | T | G | 2 | a0001c0002t0009g0245 a0001c0002t0009g0334 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1211+6466T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481249 | |||||||
| chr10:94481275 | AAG | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6493_1211+649 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481275 | |||||||
| chr10:94481283 | A | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6500A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481283 | |||||||
| chr10:94481285 | T | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6502T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481285 | |||||||
| chr10:94481286 | G | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6503G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481286 | |||||||
| chr10:94481288 | CTTCTGTC others(160): Show |
C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6506_1211+667 others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481288 | |||||||
| chr10:94481564 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1211+6781A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481564 | |||||||
| chr10:94481678 | C | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1211+6895C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481678 | |||||||
| chr10:94481790 | C | CT | 170 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1211+7017dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94481790 | ||||||
| chr10:94481801 | A | T | 196 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1211+7018A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481801 | |||||||
| chr10:94482076 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1211+7293G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482076 | |||||||
| chr10:94482132 | C | T | 187 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1211+7349C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482132 | |||||||
| chr10:94482159 | C | A | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1211+7376C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482159 | |||||||
| chr10:94482316 | GGTTCCCG others(5): Show |
G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1211+7542_1211+755 others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94482316 | ||||||
| chr10:94482692 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1211+7909C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482692 | |||||||
| chr10:94482812 | C | T | 1 | a0001c0002t0002g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1211+8029C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482812 | |||||||
| chr10:94482968 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1211+8185A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482968 | |||||||
| chr10:94483039 | C | CT | 227 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1211+8274dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483039 | ||||||
| chr10:94483039 | C | CTT | 16 | a0001c0001t0001g0111 a0001c0001t0001g0168 a0001c0001t0001g0169 others(13): Show |
17 | HG01175.hp1 HG02071.hp2 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.1211+8273_1211+827 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483039 | ||||||
| chr10:94483138 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | NA18979.hp2 NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1211+8355C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483138 | |||||||
| chr10:94483246 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1211+8463G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483246 | |||||||
| chr10:94483623 | T | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211+8840T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483623 | |||||||
| chr10:94483707 | C | T | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1211+8924C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483707 | |||||||
| chr10:94483732 | G | GT | 13 | a0001c0001t0001g0091 a0001c0001t0005g0200 a0001c0001t0005g0201 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1211+8958dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483732 | ||||||
| chr10:94483765 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0008t0001g0052 |
3 | NA18943.hp1 NA19080.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1211+8982C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483765 | |||||||
| chr10:94483943 | AT | A | 43 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(40): Show |
43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1211+9163delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483943 | ||||||
| chr10:94484060 | T | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1211+9277T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484060 | |||||||
| chr10:94484248 | GT | G | 36 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0081 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1212-9102delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94484248 | ||||||
| chr10:94484248 | GTT | G | 303 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(300): Show |
305 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1212-9103_1212-910 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94484248 | ||||||
| chr10:94484265 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-9100A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484265 | |||||||
| chr10:94484267 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1212-9098G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484267 | |||||||
| chr10:94484267 | G | C | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1212-9098G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484267 | |||||||
| chr10:94484276 | C | T | 25 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(22): Show |
25 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1212-9089C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484276 | |||||||
| chr10:94484360 | G | T | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-9005G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484360 | |||||||
| chr10:94484429 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1212-8936G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484429 | |||||||
| chr10:94484803 | T | C | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-8562T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484803 | |||||||
| chr10:94484979 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1212-8386T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484979 | |||||||
| chr10:94485544 | C | CT | 98 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(95): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1212-7803dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94485544 | ||||||
| chr10:94485576 | C | A | 46 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(43): Show |
46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1212-7789C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485576 | |||||||
| chr10:94485638 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1212-7727A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485638 | |||||||
| chr10:94485754 | A | G | 2 | a0001c0001t0004g0001 a0001c0001t0004g0219 |
3 | NA18948.hp1 NA18979.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1212-7611A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485754 | |||||||
| chr10:94485756 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1212-7609T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485756 | |||||||
| chr10:94485884 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-7481T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485884 | |||||||
| chr10:94486046 | CA | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-7312delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94486046 | ||||||
| chr10:94486115 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-7250T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486115 | |||||||
| chr10:94486136 | C | CT | 87 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(84): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1212-7227dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94486136 | ||||||
| chr10:94486138 | TC | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0121 |
3 | HG00639.hp2 NA18942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1212-7226delC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486138 | |||||||
| chr10:94486139 | C | T | 178 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1212-7226C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486139 | |||||||
| chr10:94486139 | CTTT | C | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1212-7210_1212-720 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94486139 | ||||||
| chr10:94486142 | T | C | 1 | a0001c0002t0003g0324 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1212-7223T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486142 | |||||||
| chr10:94486291 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1212-7074G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486291 | |||||||
| chr10:94486387 | T | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-6978T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486387 | |||||||
| chr10:94486697 | T | G | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1212-6668T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486697 | |||||||
| chr10:94486766 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1212-6599G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486766 | |||||||
| chr10:94486788 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6577A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486788 | |||||||
| chr10:94486834 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6531A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486834 | |||||||
| chr10:94486874 | A | C | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1212-6491A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486874 | |||||||
| chr10:94486996 | G | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-6369G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486996 | |||||||
| chr10:94487062 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6303C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487062 | |||||||
| chr10:94487123 | G | A | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-6242G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487123 | |||||||
| chr10:94487125 | C | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6240C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487125 | |||||||
| chr10:94487242 | C | CT | 154 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1212-6107dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487242 | ||||||
| chr10:94487242 | CT | C | 16 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1212-6107delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487242 | ||||||
| chr10:94487425 | A | AT | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-5930dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487425 | ||||||
| chr10:94487425 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1212-5940A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487425 | |||||||
| chr10:94487692 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-5673C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487692 | |||||||
| chr10:94487694 | C | CT | 31 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(28): Show |
32 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1212-5651dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487694 | ||||||
| chr10:94487694 | CT | C | 86 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0019 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1212-5651delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487694 | ||||||
| chr10:94487694 | CTT | C | 23 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0057 others(20): Show |
23 | HG01074.hp2 HG01358.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1212-5652_1212-565 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487694 | ||||||
| chr10:94487696 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0075 |
2 | HG00741.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1212-5669T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487696 | |||||||
| chr10:94487697 | T | C | 72 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0021 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1212-5668T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487697 | |||||||
| chr10:94487698 | T | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0057 others(9): Show |
12 | HG01074.hp2 HG01358.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1212-5667T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487698 | |||||||
| chr10:94487822 | G | C | 1 | a0001c0001t0004g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1212-5543G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487822 | |||||||
| chr10:94487863 | G | T | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-5502G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487863 | |||||||
| chr10:94487873 | T | G | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1212-5492T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487873 | |||||||
| chr10:94487874 | G | GT | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1212-5484dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487874 | ||||||
| chr10:94487874 | G | T | 2 | a0001c0001t0001g0098 a0001c0001t0006g0003 |
2 | HG02300.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1212-5491G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487874 | |||||||
| chr10:94487956 | C | A | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1212-5409C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487956 | |||||||
| chr10:94487964 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1212-5401G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487964 | |||||||
| chr10:94488080 | T | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-5285T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488080 | |||||||
| chr10:94488080 | T | G | 199 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1212-5285T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488080 | |||||||
| chr10:94488100 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1212-5265A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488100 | |||||||
| chr10:94488244 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1212-5121C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488244 | |||||||
| chr10:94488254 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1212-5111G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488254 | |||||||
| chr10:94488259 | G | A | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-5106G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488259 | |||||||
| chr10:94488278 | C | T | 1 | a0001c0002t0002g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1212-5087C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488278 | |||||||
| chr10:94488311 | A | G | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-5054A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488311 | |||||||
| chr10:94488320 | G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-5045G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488320 | |||||||
| chr10:94488386 | C | CT | 86 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1212-4957dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | ||||||
| chr10:94488386 | C | CTT | 99 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(96): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1212-4958_1212-495 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | ||||||
| chr10:94488386 | C | CTTT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0113 a0001c0001t0001g0115 others(4): Show |
7 | HG02071.hp1 HG02145.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-4959_1212-495 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | ||||||
| chr10:94488386 | CTTTTT | C | 9 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0237 others(6): Show |
9 | HG01928.hp2 HG02056.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1212-4961_1212-495 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | ||||||
| chr10:94488477 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1212-4888G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488477 | |||||||
| chr10:94488536 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-4829A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488536 | |||||||
| chr10:94488608 | TC | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-4756delC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488608 | |||||||
| chr10:94488687 | G | A | 11 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(8): Show |
12 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-4678G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488687 | |||||||
| chr10:94488726 | G | T | 2 | a0001c0002t0002g0297 a0001c0002t0002g0298 |
2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1212-4639G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488726 | |||||||
| chr10:94488879 | T | G | 203 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1212-4486T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488879 | |||||||
| chr10:94488984 | G | A | 3 | a0001c0002t0002g0228 a0001c0002t0002g0283 a0001c0002t0002g0285 |
3 | HG01981.hp2 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1212-4381G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488984 | |||||||
| chr10:94489068 | TCAGGAC | T | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1212-4295_1212-429 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94489068 | ||||||
| chr10:94489166 | C | T | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-4199C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489166 | |||||||
| chr10:94489332 | C | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-4033C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489332 | |||||||
| chr10:94489903 | C | G | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-3462C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489903 | |||||||
| chr10:94489919 | A | G | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-3446A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489919 | |||||||
| chr10:94490031 | T | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(12): Show |
15 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212-3334T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490031 | |||||||
| chr10:94490259 | AG | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(12): Show |
15 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212-3105delG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490259 | |||||||
| chr10:94490550 | A | C | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-2815A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490550 | |||||||
| chr10:94490617 | T | C | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1212-2748T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490617 | |||||||
| chr10:94490838 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1212-2527T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490838 | |||||||
| chr10:94490871 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1212-2494T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490871 | |||||||
| chr10:94490894 | T | C | 270 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1212-2471T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490894 | |||||||
| chr10:94490895 | G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-2470G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490895 | |||||||
| chr10:94490957 | G | T | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1212-2408G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490957 | |||||||
| chr10:94490979 | T | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1212-2386T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490979 | |||||||
| chr10:94491132 | A | G | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1212-2233A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491132 | |||||||
| chr10:94491153 | A | G | 1 | a0001c0001t0004g0221 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1212-2212A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491153 | |||||||
| chr10:94491229 | G | A | 1 | a0001c0001t0004g0221 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1212-2136G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491229 | |||||||
| chr10:94491363 | A | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1212-2002A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491363 | |||||||
| chr10:94491376 | C | T | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1212-1989C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491376 | |||||||
| chr10:94491411 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-1954A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491411 | |||||||
| chr10:94491502 | C | T | 9 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0237 others(6): Show |
9 | HG01928.hp2 HG02056.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1212-1863C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491502 | |||||||
| chr10:94491681 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1212-1684A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491681 | |||||||
| chr10:94491703 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-1662A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491703 | |||||||
| chr10:94491784 | TTCAAAGA others(169): Show |
T | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1212-1577_1212-140 others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94491784 | ||||||
| chr10:94491953 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0039 |
2 | NA18939.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1212-1412G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491953 | |||||||
| chr10:94492182 | A | G | 200 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1212-1183A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492182 | |||||||
| chr10:94492269 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1212-1096A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492269 | |||||||
| chr10:94492354 | TA | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-1009delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94492354 | ||||||
| chr10:94492395 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-970A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492395 | |||||||
| chr10:94492447 | G | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(3): Show |
6 | HG02698.hp2 HG03017.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-918G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492447 | |||||||
| chr10:94492458 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1212-907C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492458 | |||||||
| chr10:94492484 | A | G | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1212-881A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492484 | |||||||
| chr10:94492530 | C | A | 1 | a0001c0002t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1212-835C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492530 | |||||||
| chr10:94492536 | A | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00673.hp2 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1212-829A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492536 | |||||||
| chr10:94492556 | A | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-809A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492556 | |||||||
| chr10:94492755 | G | A | 1 | a0001c0001t0006g0005 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1212-610G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492755 | |||||||
| chr10:94492843 | T | C | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-522T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492843 | |||||||
| chr10:94493145 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1212-220T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94493145 | |||||||
| chr10:94493151 | TAC | T | 179 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1212-191_1212-190d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94493151 | ||||||
| chr10:94493151 | TACACAC | T | 13 | a0001c0002t0003g0304 a0001c0002t0003g0305 a0001c0002t0003g0309 others(10): Show |
13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1212-195_1212-190d others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94493151 | ||||||
| chr10:94493328 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1212-37T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94493328 | |||||||
| chr10:94493342 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-23A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94493342 | |||||||
| chr10:94493615 | A | T | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1294+168A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94493615 | |||||||
| chr10:94493796 | A | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+349A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94493796 | |||||||
| chr10:94494049 | G | T | 1 | a0001c0002t0003g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1294+602G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494049 | |||||||
| chr10:94494130 | T | C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1294+683T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494130 | |||||||
| chr10:94494155 | G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1294+708G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494155 | |||||||
| chr10:94494191 | T | C | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1294+744T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494191 | |||||||
| chr10:94494349 | T | C | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1294+902T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494349 | |||||||
| chr10:94494369 | C | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1294+922C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494369 | |||||||
| chr10:94494437 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1294+990G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494437 | |||||||
| chr10:94494796 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1294+1349G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494796 | |||||||
| chr10:94494960 | C | T | 2 | a0001c0002t0010g0306 a0001c0002t0010g0315 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1294+1513C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494960 | |||||||
| chr10:94495027 | C | CT | 167 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1294+1594dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr10 | 94495027 | ||||||
| chr10:94495084 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1294+1637C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94495084 | |||||||
| chr10:94495434 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0198 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1295-1621C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94495434 | |||||||
| chr10:94495723 | A | AT | 9 | a0001c0001t0011g0193 a0001c0002t0002g0228 a0001c0002t0002g0264 others(6): Show |
9 | HG01981.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1295-1322dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr10 | 94495723 | ||||||
| chr10:94495734 | G | T | 174 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1295-1321G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94495734 | |||||||
| chr10:94496057 | C | T | 1 | a0001c0002t0016g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1295-998C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496057 | |||||||
| chr10:94496065 | T | C | 1 | a0001c0002t0003g0308 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1295-990T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496065 | |||||||
| chr10:94496147 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1295-908C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496147 | |||||||
| chr10:94496204 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1295-851C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496204 | |||||||
| chr10:94496388 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1295-667T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496388 | |||||||
| chr10:94496415 | G | A | 1 | a0001c0011t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1295-640G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496415 | |||||||
| chr10:94496450 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1295-605A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496450 | |||||||
| chr10:94496813 | C | A | 1 | a0001c0004t0012g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1295-242C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496813 | |||||||
| chr10:94496930 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1295-125T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496930 | |||||||
| chr10:94496967 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1295-88A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496967 | |||||||
| chr10:94497227 | CT | C | 11 | a0001c0001t0001g0069 a0001c0001t0001g0123 a0001c0001t0001g0132 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+68delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497227 | ||||||
| chr10:94497291 | A | C | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1412+119A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497291 | |||||||
| chr10:94497468 | G | A | 3 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1412+296G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497468 | |||||||
| chr10:94497515 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0002g0269 others(4): Show |
7 | HG00323.hp1 HG02055.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+365dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497515 | ||||||
| chr10:94497515 | CT | C | 164 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1412+365delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497515 | ||||||
| chr10:94497515 | CTT | C | 8 | a0001c0001t0001g0061 a0001c0001t0002g0231 a0001c0001t0006g0004 others(5): Show |
8 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412+364_1412+365d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497515 | ||||||
| chr10:94497543 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+371G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497543 | |||||||
| chr10:94497656 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1412+484A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497656 | |||||||
| chr10:94497676 | C | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1412+504C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497676 | |||||||
| chr10:94497686 | AT | A | 201 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1412+528delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497686 | ||||||
| chr10:94497686 | ATT | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(7): Show |
11 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+527_1412+528d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497686 | ||||||
| chr10:94497821 | C | CT | 10 | a0001c0001t0001g0111 a0001c0001t0001g0130 a0001c0001t0004g0214 others(7): Show |
10 | HG01175.hp1 HG02040.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+666dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497821 | ||||||
| chr10:94497821 | CT | C | 14 | a0001c0002t0003g0304 a0001c0002t0003g0305 a0001c0002t0003g0309 others(11): Show |
14 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1412+666delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497821 | ||||||
| chr10:94497979 | T | C | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1412+807T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497979 | |||||||
| chr10:94498052 | C | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1412+880C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498052 | |||||||
| chr10:94498164 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1412+992C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498164 | |||||||
| chr10:94498346 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1412+1174G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498346 | |||||||
| chr10:94498476 | CAG | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1412+1307_1412+130 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94498476 | ||||||
| chr10:94498508 | C | T | 3 | a0001c0002t0003g0305 a0001c0002t0003g0309 a0001c0002t0003g0322 |
3 | HG03017.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1412+1336C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498508 | |||||||
| chr10:94498774 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413-1447G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498774 | |||||||
| chr10:94498790 | A | G | 46 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(43): Show |
46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1413-1431A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498790 | |||||||
| chr10:94498793 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1413-1428A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498793 | |||||||
| chr10:94498860 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413-1361C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498860 | |||||||
| chr10:94498865 | G | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413-1356G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498865 | |||||||
| chr10:94498866 | C | T | 2 | a0001c0002t0009g0245 a0001c0002t0009g0334 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1413-1355C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498866 | |||||||
| chr10:94498921 | T | C | 7 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-1300T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498921 | |||||||
| chr10:94499077 | T | A | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1413-1144T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499077 | |||||||
| chr10:94499225 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1413-996T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499225 | |||||||
| chr10:94499244 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413-977A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499244 | |||||||
| chr10:94499269 | C | G | 77 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1413-952C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499269 | |||||||
| chr10:94499529 | G | A | 2 | a0001c0002t0003g0302 a0001c0002t0003g0303 |
2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1413-692G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499529 | |||||||
| chr10:94499581 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413-640C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499581 | |||||||
| chr10:94499621 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413-600G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499621 | |||||||
| chr10:94499686 | G | A | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1413-535G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499686 | |||||||
| chr10:94499993 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-228C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499993 | |||||||
| chr10:94500046 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1413-175G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94500046 | |||||||
| chr10:94500621 | T | A | 186 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1519+294T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94500621 | |||||||
| chr10:94500748 | A | AT | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+431dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94500748 | ||||||
| chr10:94500795 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+468C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94500795 | |||||||
| chr10:94501012 | C | T | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+685C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501012 | |||||||
| chr10:94501072 | A | AAATG | 11 | a0001c0001t0001g0083 a0001c0001t0005g0203 a0001c0001t0005g0205 others(8): Show |
11 | HG01884.hp1 HG02602.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1519+769_1519+772d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501072 | ||||||
| chr10:94501072 | A | AAATGAAT others(1): Show |
9 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1519+765_1519+772d others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501072 | ||||||
| chr10:94501092 | G | GAATA | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1519+768_1519+769i others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501092 | ||||||
| chr10:94501096 | G | A | 40 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(37): Show |
41 | HG01884.hp2 HG01891.hp1 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.1519+769G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501096 | |||||||
| chr10:94501096 | G | GAATA | 158 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1519+788_1519+791d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501096 | ||||||
| chr10:94501100 | A | G | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+773A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501100 | |||||||
| chr10:94501375 | T | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1519+1048T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501375 | |||||||
| chr10:94501442 | A | C | 2 | a0001c0002t0003g0304 a0001c0002t0003g0310 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1519+1115A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501442 | |||||||
| chr10:94501481 | T | C | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+1154T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501481 | |||||||
| chr10:94501651 | A | T | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1519+1324A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501651 | |||||||
| chr10:94501787 | A | G | 2 | a0001c0001t0001g0135 a0002c0006t0013g0344 |
2 | HG02257.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1519+1460A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501787 | |||||||
| chr10:94501792 | C | T | 20 | a0001c0002t0003g0304 a0001c0002t0003g0305 a0001c0002t0003g0308 others(17): Show |
20 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1519+1465C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501792 | |||||||
| chr10:94502102 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1519+1775G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502102 | |||||||
| chr10:94502177 | A | G | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+1850A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502177 | |||||||
| chr10:94502246 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1519+1919C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502246 | |||||||
| chr10:94502319 | C | T | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1519+1992C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502319 | |||||||
| chr10:94502473 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1519+2146G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502473 | |||||||
| chr10:94502476 | G | A | 5 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(2): Show |
5 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1519+2149G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502476 | |||||||
| chr10:94502573 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0014g0125 |
3 | HG00423.hp1 HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1519+2246G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502573 | |||||||
| chr10:94502870 | G | A | 1 | a0001c0002t0003g0325 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1519+2543G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502870 | |||||||
| chr10:94502979 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+2652G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502979 | |||||||
| chr10:94503243 | A | G | 1 | a0001c0002t0003g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1519+2916A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503243 | |||||||
| chr10:94503416 | C | G | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+3089C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503416 | |||||||
| chr10:94503439 | T | G | 1 | a0001c0002t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1519+3112T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503439 | |||||||
| chr10:94503476 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1519+3149A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503476 | |||||||
| chr10:94503663 | C | T | 1 | a0003c0009t0006g0008 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1519+3336C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503663 | |||||||
| chr10:94503664 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+3337G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503664 | |||||||
| chr10:94503777 | C | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1519+3450C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503777 | |||||||
| chr10:94503895 | G | A | 5 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 others(2): Show |
5 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520-3372G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503895 | |||||||
| chr10:94503896 | C | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1520-3371C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503896 | |||||||
| chr10:94504029 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1520-3238G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504029 | |||||||
| chr10:94504320 | T | C | 20 | a0001c0002t0003g0304 a0001c0002t0003g0305 a0001c0002t0003g0308 others(17): Show |
20 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1520-2947T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504320 | |||||||
| chr10:94504324 | A | G | 5 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0105 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520-2943A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504324 | |||||||
| chr10:94504374 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1520-2893C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504374 | |||||||
| chr10:94504415 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1520-2852T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504415 | |||||||
| chr10:94504500 | T | G | 270 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1520-2767T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504500 | |||||||
| chr10:94504531 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1520-2736T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504531 | |||||||
| chr10:94504590 | A | G | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1520-2677A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504590 | |||||||
| chr10:94504708 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1520-2559T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504708 | |||||||
| chr10:94505178 | A | T | 2 | a0001c0002t0002g0253 a0001c0002t0002g0267 |
2 | NA18959.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1520-2089A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505178 | |||||||
| chr10:94505263 | C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1520-2004C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505263 | |||||||
| chr10:94505512 | G | A | 1 | a0001c0002t0003g0305 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1520-1755G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505512 | |||||||
| chr10:94505606 | G | GT | 14 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1520-1650dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94505606 | ||||||
| chr10:94505817 | C | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1520-1450C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505817 | |||||||
| chr10:94506041 | A | AT | 258 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1520-1212dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94506041 | ||||||
| chr10:94506041 | A | ATT | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1520-1213_1520-121 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94506041 | ||||||
| chr10:94506277 | G | A | 1 | a0001c0002t0003g0308 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1520-990G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506277 | |||||||
| chr10:94506286 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1520-981G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506286 | |||||||
| chr10:94506371 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1520-896G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506371 | |||||||
| chr10:94506796 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1520-471A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506796 | |||||||
| chr10:94507647 | T | C | 6 | a0001c0002t0002g0248 a0001c0002t0002g0284 a0001c0002t0002g0294 others(3): Show |
6 | HG00323.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+300T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507647 | |||||||
| chr10:94507648 | G | A | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1600+301G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507648 | |||||||
| chr10:94507657 | A | C | 6 | a0001c0002t0002g0248 a0001c0002t0002g0284 a0001c0002t0002g0294 others(3): Show |
6 | HG00323.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+310A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507657 | |||||||
| chr10:94507811 | C | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1600+464C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507811 | |||||||
| chr10:94507843 | G | A | 5 | a0001c0001t0001g0021 a0001c0002t0002g0294 a0001c0002t0002g0295 others(2): Show |
5 | HG00323.hp2 HG00438.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1600+496G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507843 | |||||||
| chr10:94508057 | G | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1600+710G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508057 | |||||||
| chr10:94508418 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1600+1071A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508418 | |||||||
| chr10:94508439 | T | TTC | 3 | a0001c0001t0001g0048 a0001c0001t0001g0161 a0001c0001t0005g0200 |
3 | HG02056.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1600+1112_1600+111 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94508439 | ||||||
| chr10:94508724 | C | A | 1 | a0001c0002t0003g0302 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1601-1367C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508724 | |||||||
| chr10:94508761 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1601-1330A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508761 | |||||||
| chr10:94508803 | T | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1601-1288T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508803 | |||||||
| chr10:94508821 | G | A | 2 | a0001c0002t0002g0297 a0001c0002t0002g0298 |
2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1601-1270G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508821 | |||||||
| chr10:94509107 | G | GT | 28 | a0001c0001t0002g0025 a0001c0001t0002g0240 a0001c0001t0002g0244 others(25): Show |
28 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1601-965dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94509107 | ||||||
| chr10:94509107 | GT | G | 147 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1601-965delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94509107 | ||||||
| chr10:94509126 | T | G | 1 | a0001c0003t0008g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1601-965T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509126 | |||||||
| chr10:94509130 | A | G | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1601-961A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509130 | |||||||
| chr10:94509252 | G | A | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1601-839G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509252 | |||||||
| chr10:94509317 | G | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | HG00639.hp2 HG01123.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601-774G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509317 | |||||||
| chr10:94509337 | T | TCCAC | 339 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1601-751_1601-750i others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94509337 | ||||||
| chr10:94509389 | G | A | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601-702G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509389 | |||||||
| chr10:94509529 | A | T | 1 | a0001c0002t0002g0276 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1601-562A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509529 | |||||||
| chr10:94509637 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-454C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509637 | |||||||
| chr10:94509651 | A | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-440A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509651 | |||||||
| chr10:94509676 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1601-415C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509676 | |||||||
| chr10:94509750 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1601-341A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509750 | |||||||
| chr10:94510035 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1601-56A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94510035 | |||||||
| chr10:94510305 | T | C | 3 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0204 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1689+126T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510305 | |||||||
| chr10:94510347 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1689+168A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510347 | |||||||
| chr10:94510367 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1689+188G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510367 | |||||||
| chr10:94510438 | G | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1689+259G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510438 | |||||||
| chr10:94510446 | T | G | 1 | a0001c0002t0002g0252 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1689+267T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510446 | |||||||
| chr10:94510608 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+429C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510608 | |||||||
| chr10:94510893 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1690-690A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510893 | |||||||
| chr10:94510955 | A | G | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1690-628A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510955 | |||||||
| chr10:94511095 | CT | C | 293 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0017 others(290): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1690-466delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 94511095 | ||||||
| chr10:94511095 | CTT | C | 16 | a0001c0001t0001g0046 a0001c0001t0001g0108 a0001c0001t0001g0123 others(13): Show |
16 | HG00323.hp2 HG01256.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690-467_1690-466d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 94511095 | ||||||
| chr10:94511416 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1690-167T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94511416 | |||||||
| chr10:94511541 | A | C | 340 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(337): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1690-42A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94511541 | |||||||
| chr10:94512083 | C | A | 181 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1761+429C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512083 | |||||||
| chr10:94512125 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1761+471C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512125 | |||||||
| chr10:94512181 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1761+527A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512181 | |||||||
| chr10:94512234 | A | G | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1761+580A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512234 | |||||||
| chr10:94512279 | G | A | 1 | a0001c0002t0002g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1761+625G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512279 | |||||||
| chr10:94512289 | A | AT | 171 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1761+641dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94512289 | ||||||
| chr10:94512858 | A | T | 192 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1761+1204A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512858 | |||||||
| chr10:94513162 | G | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761+1508G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513162 | |||||||
| chr10:94513212 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1761+1558A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513212 | |||||||
| chr10:94513247 | C | CA | 222 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1761+1594dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94513247 | ||||||
| chr10:94513247 | C | CAA | 10 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(7): Show |
11 | HG01978.hp1 HG02071.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1761+1594_1761+159 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94513247 | ||||||
| chr10:94513247 | C | CAAA | 5 | a0001c0001t0004g0215 a0001c0001t0004g0219 a0001c0003t0008g0012 others(2): Show |
5 | HG02258.hp1 HG02922.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+1594_1761+159 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94513247 | ||||||
| chr10:94513249 | C | A | 341 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(338): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1761+1595C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513249 | |||||||
| chr10:94513364 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1761+1710T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513364 | |||||||
| chr10:94513447 | A | G | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1761+1793A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513447 | |||||||
| chr10:94513455 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1761+1801A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513455 | |||||||
| chr10:94513685 | T | C | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761+2031T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513685 | |||||||
| chr10:94513885 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1761+2231G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513885 | |||||||
| chr10:94514038 | TCAAAAAA others(4): Show |
T | 1 | a0001c0002t0002g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1761+2396_1761+240 others(15): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514038 | ||||||
| chr10:94514039 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1761+2385C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514039 | |||||||
| chr10:94514050 | C | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0070 a0001c0001t0005g0208 |
3 | HG02145.hp1 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1761+2396C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514050 | |||||||
| chr10:94514050 | CA | C | 172 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1761+2409delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514050 | ||||||
| chr10:94514051 | A | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0070 a0001c0001t0005g0208 |
3 | HG02145.hp1 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1761+2397A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514051 | |||||||
| chr10:94514053 | A | C | 1 | a0001c0002t0002g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1761+2399A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514053 | |||||||
| chr10:94514055 | A | C | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761+2401A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514055 | |||||||
| chr10:94514088 | CTGTAATC others(7): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1761+2460_1761+247 others(18): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514088 | ||||||
| chr10:94514340 | G | A | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1761+2686G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514340 | |||||||
| chr10:94514397 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1761+2743C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514397 | |||||||
| chr10:94514512 | G | A | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1761+2858G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514512 | |||||||
| chr10:94514750 | C | T | 259 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1761+3096C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514750 | |||||||
| chr10:94514803 | T | C | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1761+3149T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514803 | |||||||
| chr10:94514907 | C | CT | 29 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0048 others(26): Show |
29 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1761+3271dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514907 | ||||||
| chr10:94514907 | C | T | 1 | a0001c0001t0021g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1761+3253C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514907 | |||||||
| chr10:94514907 | CT | C | 16 | a0001c0001t0001g0075 a0001c0001t0001g0184 a0001c0001t0001g0186 others(13): Show |
16 | HG00741.hp2 HG01891.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1761+3271delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514907 | ||||||
| chr10:94514911 | T | C | 1 | a0001c0002t0003g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1761+3257T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514911 | |||||||
| chr10:94514924 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1761+3270T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514924 | |||||||
| chr10:94514930 | C | T | 1 | a0001c0001t0021g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1761+3276C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514930 | |||||||
| chr10:94515015 | C | T | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1761+3361C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515015 | |||||||
| chr10:94515139 | C | T | 1 | a0001c0001t0005g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1761+3485C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515139 | |||||||
| chr10:94515153 | C | T | 2 | a0001c0002t0003g0230 a0001c0002t0003g0324 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1761+3499C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515153 | |||||||
| chr10:94515199 | G | A | 4 | a0001c0002t0002g0259 a0001c0002t0002g0278 a0001c0002t0002g0287 others(1): Show |
4 | HG02129.hp1 HG02523.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1761+3545G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515199 | |||||||
| chr10:94515272 | A | C | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1761+3618A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515272 | |||||||
| chr10:94515282 | C | T | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1761+3628C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515282 | |||||||
| chr10:94515335 | G | GT | 12 | a0001c0001t0001g0146 a0001c0001t0005g0200 a0001c0001t0005g0201 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761+3688dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94515335 | ||||||
| chr10:94515343 | G | T | 199 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1761+3689G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515343 | |||||||
| chr10:94515578 | A | G | 2 | a0001c0002t0009g0245 a0001c0002t0009g0334 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1761+3924A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515578 | |||||||
| chr10:94515707 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1761+4053A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515707 | |||||||
| chr10:94515732 | A | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1761+4078A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515732 | |||||||
| chr10:94515764 | C | A | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1761+4110C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515764 | |||||||
| chr10:94515915 | A | ACAG | 197 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1761+4263_1761+426 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94515915 | ||||||
| chr10:94516072 | A | AC | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1761+4420dupC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94516072 | ||||||
| chr10:94516115 | G | A | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1761+4461G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516115 | |||||||
| chr10:94516188 | C | A | 157 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1761+4534C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516188 | |||||||
| chr10:94516413 | CTTTT | C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761+4763_1761+476 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94516413 | ||||||
| chr10:94516430 | A | T | 2 | a0001c0001t0001g0119 a0001c0001t0002g0242 |
2 | HG01099.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1761+4776A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516430 | |||||||
| chr10:94516462 | C | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1761+4808C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516462 | |||||||
| chr10:94516466 | G | C | 1 | a0001c0001t0025g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1761+4812G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516466 | |||||||
| chr10:94516568 | T | C | 1 | a0001c0002t0009g0334 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1761+4914T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516568 | |||||||
| chr10:94516660 | A | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1761+5006A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516660 | |||||||
| chr10:94516686 | C | A | 1 | a0001c0001t0021g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1761+5032C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516686 | |||||||
| chr10:94516911 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-5044G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516911 | |||||||
| chr10:94517197 | C | G | 17 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(14): Show |
18 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.1762-4758C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517197 | |||||||
| chr10:94517247 | G | A | 1 | a0001c0002t0002g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1762-4708G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517247 | |||||||
| chr10:94517277 | C | G | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1762-4678C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517277 | |||||||
| chr10:94517400 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0241 |
3 | HG01516.hp2 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1762-4555C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517400 | |||||||
| chr10:94517458 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1762-4497C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517458 | |||||||
| chr10:94517594 | TAA | T | 9 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0215 others(6): Show |
10 | HG02071.hp2 NA18948.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762-4359_1762-435 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94517594 | ||||||
| chr10:94517735 | G | A | 1 | a0001c0002t0003g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1762-4220G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517735 | |||||||
| chr10:94517740 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1762-4215T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517740 | |||||||
| chr10:94517783 | C | CA | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0015g0092 |
3 | HG00423.hp2 NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1762-4171dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94517783 | ||||||
| chr10:94517881 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1762-4074G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517881 | |||||||
| chr10:94517974 | G | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1762-3981G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517974 | |||||||
| chr10:94518050 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-3905G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518050 | |||||||
| chr10:94518118 | C | T | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1762-3837C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518118 | |||||||
| chr10:94518145 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1762-3810T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518145 | |||||||
| chr10:94518234 | A | G | 197 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1762-3721A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518234 | |||||||
| chr10:94518638 | G | A | 166 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1762-3317G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518638 | |||||||
| chr10:94518772 | A | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-3183A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518772 | |||||||
| chr10:94518813 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1762-3142G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518813 | |||||||
| chr10:94518814 | C | G | 1 | a0001c0001t0006g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1762-3141C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518814 | |||||||
| chr10:94518967 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1762-2988C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518967 | |||||||
| chr10:94519001 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1762-2954G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519001 | |||||||
| chr10:94519412 | C | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1762-2543C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519412 | |||||||
| chr10:94519569 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1762-2386A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519569 | |||||||
| chr10:94519604 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1762-2351C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519604 | |||||||
| chr10:94519633 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1762-2322A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519633 | |||||||
| chr10:94519641 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-2314G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519641 | |||||||
| chr10:94519679 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1762-2276A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519679 | |||||||
| chr10:94519705 | A | G | 46 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(43): Show |
46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1762-2250A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519705 | |||||||
| chr10:94519716 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1762-2239A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519716 | |||||||
| chr10:94520274 | C | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1762-1681C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520274 | |||||||
| chr10:94520382 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0021g0272 |
2 | HG01123.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1762-1573G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520382 | |||||||
| chr10:94520491 | C | T | 43 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 others(40): Show |
43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1762-1464C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520491 | |||||||
| chr10:94520536 | G | A | 181 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1762-1419G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520536 | |||||||
| chr10:94520558 | A | T | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1762-1397A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520558 | |||||||
| chr10:94520559 | T | TA | 161 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1762-1389dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94520559 | ||||||
| chr10:94520700 | C | A | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1762-1255C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520700 | |||||||
| chr10:94520709 | G | T | 2 | a0001c0002t0003g0311 a0001c0002t0003g0312 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1762-1246G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520709 | |||||||
| chr10:94520724 | A | G | 1 | a0001c0001t0014g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1762-1231A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520724 | |||||||
| chr10:94520805 | A | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1762-1150A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520805 | |||||||
| chr10:94520952 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1762-1003C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520952 | |||||||
| chr10:94520953 | G | A | 1 | a0001c0002t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1762-1002G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520953 | |||||||
| chr10:94521203 | G | A | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1762-752G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521203 | |||||||
| chr10:94521221 | C | CA | 8 | a0001c0001t0001g0047 a0001c0001t0001g0142 a0001c0001t0001g0161 others(5): Show |
8 | HG00280.hp1 HG02056.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1762-718dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94521221 | ||||||
| chr10:94521221 | CA | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0069 others(9): Show |
12 | HG02040.hp2 HG02109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1762-718delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94521221 | ||||||
| chr10:94521231 | A | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1762-724A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521231 | |||||||
| chr10:94521233 | A | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-722A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521233 | |||||||
| chr10:94521236 | A | AC | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1762-719_1762-718i others(3): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521236 | |||||||
| chr10:94521237 | A | C | 4 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 others(1): Show |
4 | HG02630.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-718A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521237 | |||||||
| chr10:94521238 | C | A | 14 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(11): Show |
14 | HG01884.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1762-717C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521238 | |||||||
| chr10:94521238 | C | CA | 43 | a0001c0001t0001g0031 a0001c0001t0002g0231 a0001c0002t0002g0225 others(40): Show |
43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1762-707dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94521238 | ||||||
| chr10:94521239 | A | C | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1762-716A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521239 | |||||||
| chr10:94521346 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1762-609C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521346 | |||||||
| chr10:94521500 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1762-455C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521500 | |||||||
| chr10:94521506 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0115 |
3 | HG02071.hp1 NA18942.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1762-449C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521506 | |||||||
| chr10:94521544 | T | C | 1 | a0001c0001t0024g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1762-411T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521544 | |||||||
| chr10:94521688 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1762-267T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521688 | |||||||
| chr10:94521788 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1762-167C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521788 | |||||||
| chr10:94521895 | A | C | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1762-60A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521895 | |||||||
| chr10:94521918 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1762-37G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521918 | |||||||
| chr10:94522245 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1891-99A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 10/12 | chr10 | 94522245 | |||||||
| chr10:94522259 | C | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-85C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 10/12 | chr10 | 94522259 | |||||||
| chr10:94522465 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2000+12C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522465 | |||||||
| chr10:94522565 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2000+112C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522565 | |||||||
| chr10:94522633 | G | A | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2000+180G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522633 | |||||||
| chr10:94522662 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000+209C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522662 | |||||||
| chr10:94522686 | G | T | 1 | a0001c0002t0002g0298 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2000+233G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522686 | |||||||
| chr10:94522785 | G | A | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2000+332G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522785 | |||||||
| chr10:94522844 | A | G | 259 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2000+391A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522844 | |||||||
| chr10:94523043 | C | CA | 159 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(156): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2000+610dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523043 | ||||||
| chr10:94523043 | C | CAA | 9 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0064 others(6): Show |
9 | HG01261.hp2 HG01433.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2000+609_2000+610d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523043 | ||||||
| chr10:94523043 | CA | C | 10 | a0001c0001t0001g0189 a0001c0001t0002g0271 a0001c0001t0002g0279 others(7): Show |
10 | HG01169.hp2 HG01981.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2000+610delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523043 | ||||||
| chr10:94523064 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2000+611G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523064 | |||||||
| chr10:94523097 | G | A | 2 | a0001c0002t0009g0245 a0001c0002t0009g0334 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2000+644G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523097 | |||||||
| chr10:94523177 | A | AGCGAAAC others(3292): Show |
1 | a0001c0001t0001g0121 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2000+734_2000+735i others(3301): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523177 | ||||||
| chr10:94523186 | C | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2000+733C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523186 | |||||||
| chr10:94523192 | C | CA | 37 | a0001c0001t0001g0024 a0001c0001t0001g0059 a0001c0001t0001g0088 others(34): Show |
37 | HG00140.hp1 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.2000+764dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | ||||||
| chr10:94523192 | C | CAA | 76 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(73): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2000+763_2000+764d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | ||||||
| chr10:94523192 | C | CAAAA | 65 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(62): Show |
65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2000+761_2000+764d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | ||||||
| chr10:94523192 | C | CAAAAA | 8 | a0001c0001t0001g0103 a0001c0001t0001g0127 a0001c0001t0001g0129 others(5): Show |
8 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+760_2000+764d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | ||||||
| chr10:94523192 | CA | C | 6 | a0001c0001t0001g0170 a0001c0001t0019g0020 a0001c0002t0002g0248 others(3): Show |
6 | HG01069.hp2 HG02735.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000+764delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | ||||||
| chr10:94523217 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2000+764A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523217 | |||||||
| chr10:94523491 | T | C | 68 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2000+1038T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523491 | |||||||
| chr10:94523749 | G | A | 18 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(15): Show |
19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.2000+1296G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523749 | |||||||
| chr10:94524091 | A | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.2000+1638A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524091 | |||||||
| chr10:94524171 | G | A | 189 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2000+1718G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524171 | |||||||
| chr10:94524263 | T | C | 1 | a0001c0002t0003g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2000+1810T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524263 | |||||||
| chr10:94524323 | C | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000+1870C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524323 | |||||||
| chr10:94524495 | C | G | 8 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000+2042C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524495 | |||||||
| chr10:94524552 | A | C | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2000+2099A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524552 | |||||||
| chr10:94524557 | G | A | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+2104G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524557 | |||||||
| chr10:94524581 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2000+2128A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524581 | |||||||
| chr10:94524674 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2000+2221G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524674 | |||||||
| chr10:94524728 | TA | T | 6 | a0001c0001t0001g0123 a0001c0001t0002g0243 a0001c0001t0018g0038 others(3): Show |
6 | HG01256.hp2 HG03017.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000+2292delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94524728 | ||||||
| chr10:94524766 | C | A | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2000+2313C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524766 | |||||||
| chr10:94524826 | T | A | 2 | a0001c0002t0007g0319 a0002c0006t0013g0344 |
2 | HG02257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2000+2373T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524826 | |||||||
| chr10:94524855 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2000+2402C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524855 | |||||||
| chr10:94524887 | C | T | 5 | a0001c0002t0003g0230 a0001c0002t0003g0316 a0001c0002t0003g0318 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2000+2434C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524887 | |||||||
| chr10:94525030 | T | C | 1 | a0001c0001t0004g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2000+2577T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525030 | |||||||
| chr10:94525147 | A | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2000+2694A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525147 | |||||||
| chr10:94525386 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2000+2933C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525386 | |||||||
| chr10:94525392 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02300.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2000+2939A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525392 | |||||||
| chr10:94525481 | G | A | 1 | a0001c0001t0005g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2000+3028G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525481 | |||||||
| chr10:94525497 | G | A | 158 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2000+3044G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525497 | |||||||
| chr10:94525567 | C | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+3114C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525567 | |||||||
| chr10:94525589 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2000+3136G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525589 | |||||||
| chr10:94525659 | C | CA | 65 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0070 others(62): Show |
65 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2000+3225dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94525659 | ||||||
| chr10:94525694 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2000+3241C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525694 | |||||||
| chr10:94525717 | G | GTATA | 5 | a0001c0002t0003g0230 a0001c0002t0003g0316 a0001c0002t0003g0318 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2000+3266_2000+326 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94525717 | ||||||
| chr10:94525756 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2000+3303T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525756 | |||||||
| chr10:94525810 | TA | T | 3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2000+3358delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525810 | |||||||
| chr10:94525811 | A | G | 1 | a0001c0002t0003g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2000+3358A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525811 | |||||||
| chr10:94525921 | C | T | 1 | a0001c0002t0003g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2000+3468C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525921 | |||||||
| chr10:94525972 | A | G | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+3519A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525972 | |||||||
| chr10:94525993 | A | G | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2000+3540A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525993 | |||||||
| chr10:94526157 | T | C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000+3704T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526157 | |||||||
| chr10:94526251 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2000+3798C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526251 | |||||||
| chr10:94526262 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(1): Show |
4 | HG02698.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000+3809C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526262 | |||||||
| chr10:94526444 | A | G | 15 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(12): Show |
15 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2000+3991A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526444 | |||||||
| chr10:94526568 | T | C | 171 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2000+4115T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526568 | |||||||
| chr10:94526647 | CAGGTTGA others(6): Show |
C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2000+4196_2000+420 others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94526647 | ||||||
| chr10:94526685 | G | A | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2000+4232G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526685 | |||||||
| chr10:94526805 | C | T | 11 | a0001c0001t0004g0001 a0001c0001t0004g0213 a0001c0001t0004g0214 others(8): Show |
12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000+4352C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526805 | |||||||
| chr10:94526922 | A | G | 2 | a0001c0001t0011g0193 a0001c0001t0011g0199 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2001-4280A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526922 | |||||||
| chr10:94527082 | T | TTG | 9 | a0001c0001t0001g0195 a0001c0002t0007g0234 a0001c0002t0007g0235 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2001-4097_2001-409 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTG | 160 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2001-4101_2001-409 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0046 others(3): Show |
6 | HG00323.hp1 HG00423.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-4103_2001-409 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0004g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2001-4105_2001-409 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2001-4115_2001-409 others(24): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(17): Show |
1 | a0001c0001t0005g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2001-4119_2001-409 others(28): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(19): Show |
5 | a0001c0001t0005g0208 a0001c0001t0005g0209 a0001c0001t0005g0210 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(30): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(21): Show |
1 | a0001c0001t0005g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2001-4096_2001-409 others(32): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(23): Show |
4 | a0001c0001t0001g0343 a0001c0001t0005g0202 a0001c0001t0005g0204 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(34): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(25): Show |
4 | a0001c0001t0001g0341 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(36): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527082 | T | TTGTGTGT others(27): Show |
2 | a0001c0001t0001g0342 a0001c0001t0005g0206 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(38): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | ||||||
| chr10:94527127 | C | T | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-4075C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527127 | |||||||
| chr10:94527279 | G | A | 160 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.2001-3923G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527279 | |||||||
| chr10:94527284 | C | T | 7 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-3918C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527284 | |||||||
| chr10:94527396 | T | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2001-3806T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527396 | |||||||
| chr10:94527500 | G | T | 17 | a0001c0001t0002g0229 a0001c0001t0002g0258 a0001c0001t0002g0260 others(14): Show |
17 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2001-3702G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527500 | |||||||
| chr10:94527500 | GT | G | 88 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0102 others(85): Show |
89 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.2001-3691delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527500 | ||||||
| chr10:94527501 | T | G | 150 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.2001-3701T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527501 | |||||||
| chr10:94527502 | T | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0102 |
3 | HG00639.hp1 HG01433.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2001-3700T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527502 | |||||||
| chr10:94527511 | T | A | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-3691T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527511 | |||||||
| chr10:94527549 | T | G | 1 | a0001c0001t0002g0288 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2001-3653T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527549 | |||||||
| chr10:94527622 | A | G | 1 | a0001c0002t0002g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2001-3580A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527622 | |||||||
| chr10:94527732 | C | T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2001-3470C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527732 | |||||||
| chr10:94528094 | G | T | 3 | a0001c0001t0011g0193 a0001c0001t0011g0199 a0001c0001t0019g0020 |
3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2001-3108G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528094 | |||||||
| chr10:94528164 | G | T | 1 | a0001c0002t0003g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2001-3038G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528164 | |||||||
| chr10:94528327 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2001-2875T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528327 | |||||||
| chr10:94528697 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2001-2505C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528697 | |||||||
| chr10:94528822 | CA | C | 6 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(3): Show |
6 | HG01884.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-2365delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94528822 | ||||||
| chr10:94528860 | A | AG | 340 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(337): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2001-2337dupG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94528860 | ||||||
| chr10:94529009 | A | AT | 20 | a0001c0001t0001g0151 a0001c0002t0003g0304 a0001c0002t0003g0305 others(17): Show |
20 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2001-2182dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94529009 | ||||||
| chr10:94529241 | C | T | 1 | a0001c0001t0017g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2001-1961C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529241 | |||||||
| chr10:94529416 | C | T | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001-1786C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529416 | |||||||
| chr10:94529479 | G | A | 7 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-1723G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529479 | |||||||
| chr10:94529501 | A | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2001-1701A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529501 | |||||||
| chr10:94529510 | C | T | 2 | a0001c0002t0002g0297 a0001c0002t0002g0298 |
2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2001-1692C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529510 | |||||||
| chr10:94529595 | G | A | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2001-1607G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529595 | |||||||
| chr10:94529652 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2001-1550G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529652 | |||||||
| chr10:94529660 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001-1542A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529660 | |||||||
| chr10:94529703 | A | G | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2001-1499A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529703 | |||||||
| chr10:94529772 | G | A | 192 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2001-1430G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529772 | |||||||
| chr10:94529866 | C | G | 2 | a0001c0004t0012g0211 a0001c0004t0012g0212 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2001-1336C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529866 | |||||||
| chr10:94529999 | C | T | 79 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2001-1203C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529999 | |||||||
| chr10:94530115 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2001-1087C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530115 | |||||||
| chr10:94530156 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2001-1046A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530156 | |||||||
| chr10:94530213 | T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2001-989T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530213 | |||||||
| chr10:94530214 | A | G | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001-988A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530214 | |||||||
| chr10:94530274 | A | G | 1 | a0001c0002t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2001-928A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530274 | |||||||
| chr10:94530400 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2001-802A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530400 | |||||||
| chr10:94530464 | T | G | 1 | a0001c0002t0003g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2001-738T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530464 | |||||||
| chr10:94530553 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2001-649G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530553 | |||||||
| chr10:94530554 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2001-648T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530554 | |||||||
| chr10:94530699 | T | C | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2001-503T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530699 | |||||||
| chr10:94530720 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2001-482C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530720 | |||||||
| chr10:94530854 | C | CT | 13 | a0001c0001t0001g0197 a0001c0001t0002g0231 a0001c0001t0004g0221 others(10): Show |
13 | HG01069.hp1 HG01099.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2001-326dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94530854 | ||||||
| chr10:94530854 | CT | C | 168 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2001-326delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94530854 | ||||||
| chr10:94530854 | CTT | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0091 a0001c0001t0001g0114 others(4): Show |
7 | HG00099.hp2 HG02258.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-327_2001-326d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94530854 | ||||||
| chr10:94530897 | A | G | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2001-305A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530897 | |||||||
| chr10:94531639 | C | CTTATT | 63 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0126 others(60): Show |
64 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2259+224_2259+228d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | ||||||
| chr10:94531639 | C | CTTATTTT others(3): Show |
5 | a0001c0002t0002g0232 a0001c0002t0002g0233 a0001c0002t0002g0327 others(2): Show |
5 | HG01109.hp1 HG02056.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2259+219_2259+228d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | ||||||
| chr10:94531639 | CTTATT | C | 108 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(105): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2259+224_2259+228d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | ||||||
| chr10:94531639 | CTTATTTT others(3): Show |
C | 22 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(19): Show |
23 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259+219_2259+228d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | ||||||
| chr10:94531674 | T | G | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2259+214T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531674 | |||||||
| chr10:94531679 | T | G | 91 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(88): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2259+219T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531679 | |||||||
| chr10:94531679 | T | TTTATTTT others(3): Show |
19 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(16): Show |
19 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2259+234_2259+243d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531679 | ||||||
| chr10:94531699 | GTTATGTT others(3): Show |
G | 69 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(66): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.2259+269_2259+278d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531699 | ||||||
| chr10:94531704 | G | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(15): Show |
18 | HG00639.hp1 HG01978.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.2259+244G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531704 | |||||||
| chr10:94531709 | T | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(15): Show |
18 | HG00639.hp1 HG01978.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.2259+249T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531709 | |||||||
| chr10:94531719 | T | TTTATG | 82 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(79): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2259+264_2259+268d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531719 | ||||||
| chr10:94531729 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+269T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531729 | |||||||
| chr10:94531729 | TTTATGTT others(3): Show |
T | 1 | a0001c0002t0002g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2259+274_2259+283d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531729 | ||||||
| chr10:94531734 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+274G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531734 | |||||||
| chr10:94531739 | G | T | 82 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(79): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2259+279G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531739 | |||||||
| chr10:94531739 | GTTATTTT others(13): Show |
G | 1 | a0001c0001t0006g0010 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2259+289_2259+308d others(22): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531739 | ||||||
| chr10:94531744 | TTTATG | T | 7 | a0001c0001t0006g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(4): Show |
7 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259+289_2259+293d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531744 | ||||||
| chr10:94531749 | G | GTTATTTT others(8): Show |
3 | a0001c0002t0003g0182 a0001c0002t0003g0302 a0001c0002t0003g0303 |
3 | HG01192.hp1 HG02735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2259+298_2259+299i others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531749 | ||||||
| chr10:94531749 | G | T | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2259+289G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531749 | |||||||
| chr10:94531759 | T | G | 126 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(123): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2259+299T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531759 | |||||||
| chr10:94531759 | T | TTTATTTT others(8): Show |
5 | a0001c0001t0002g0240 a0001c0001t0002g0244 a0001c0002t0002g0294 others(2): Show |
5 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2259+389_2259+403d others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | ||||||
| chr10:94531759 | T | TTTATTTT others(23): Show |
1 | a0001c0002t0002g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2259+374_2259+403d others(32): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | ||||||
| chr10:94531759 | T | TTTATTTT others(21): Show |
3 | a0001c0003t0008g0012 a0001c0003t0008g0013 a0001c0003t0008g0014 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2259+326_2259+327i others(30): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | ||||||
| chr10:94531759 | TTTATTTT others(8): Show |
T | 1 | a0002c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2259+389_2259+403d others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | ||||||
| chr10:94531764 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+304T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531764 | |||||||
| chr10:94531764 | T | TTTATTTT others(3): Show |
12 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2259+314_2259+323d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531764 | ||||||
| chr10:94531769 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0167 |
2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2259+309T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531769 | |||||||
| chr10:94531774 | G | T | 2 | a0001c0001t0001g0099 a0001c0001t0006g0010 |
2 | HG03834.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2259+314G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531774 | |||||||
| chr10:94531779 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+319T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531779 | |||||||
| chr10:94531782 | A | C | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+322A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531782 | |||||||
| chr10:94531789 | G | GTTATTTT others(3): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2259+334_2259+343d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531789 | ||||||
| chr10:94531794 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+334T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531794 | |||||||
| chr10:94531809 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+349T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531809 | |||||||
| chr10:94531845 | T | TTA | 22 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0060 others(19): Show |
22 | HG01243.hp1 HG01358.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2259+387_2259+388d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531845 | ||||||
| chr10:94531847 | ATGT | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0186 a0001c0001t0001g0195 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259+389_2259+391d others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531847 | ||||||
| chr10:94531847 | ATGTTATT others(1): Show |
A | 9 | a0001c0001t0001g0047 a0001c0001t0002g0231 a0001c0001t0006g0003 others(6): Show |
9 | HG00280.hp1 HG01978.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2259+389_2259+396d others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531847 | ||||||
| chr10:94531854 | T | G | 27 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0060 others(24): Show |
27 | HG01243.hp1 HG01358.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2259+394T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531854 | |||||||
| chr10:94531859 | T | G | 35 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0047 others(32): Show |
35 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.2259+399T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531859 | |||||||
| chr10:94531860 | TTA | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
32 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.2259+404_2259+405d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531860 | ||||||
| chr10:94531862 | A | ATATGT | 79 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.2259+446_2259+450d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATATGTTA others(3): Show |
36 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0028 others(33): Show |
36 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.2259+441_2259+450d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATATGTTA others(8): Show |
13 | a0001c0001t0001g0019 a0001c0001t0001g0196 a0001c0001t0001g0197 others(10): Show |
13 | HG00639.hp1 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2259+436_2259+450d others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGT | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0011g0193 |
3 | HG02895.hp1 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(6): Show |
4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(15): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(13): Show |
29 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0243 others(26): Show |
30 | HG00140.hp1 HG01069.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(22): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(18): Show |
44 | a0001c0001t0002g0002 a0001c0001t0002g0223 a0001c0001t0002g0224 others(41): Show |
45 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(27): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(23): Show |
8 | a0001c0001t0002g0271 a0001c0001t0002g0288 a0001c0002t0002g0246 others(5): Show |
8 | HG00408.hp2 HG02683.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(32): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(28): Show |
2 | a0001c0002t0002g0267 a0001c0002t0009g0245 |
2 | HG03540.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(37): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(33): Show |
3 | a0001c0001t0002g0260 a0001c0001t0002g0268 a0001c0001t0002g0279 |
3 | HG01167.hp1 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(42): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(28): Show |
2 | a0001c0002t0002g0232 a0001c0002t0002g0233 |
2 | HG02056.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(37): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(33): Show |
5 | a0001c0002t0002g0237 a0001c0002t0002g0251 a0001c0002t0002g0255 others(2): Show |
5 | HG01928.hp2 NA18973.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(42): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | A | ATGTTATT others(38): Show |
1 | a0001c0002t0002g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2259+403_2259+404i others(47): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531862 | ATATGT | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0136 a0001c0001t0001g0142 others(1): Show |
4 | HG02300.hp1 NA18956.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+446_2259+450d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | ||||||
| chr10:94531864 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+404A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531864 | |||||||
| chr10:94531866 | G | T | 3 | a0001c0001t0001g0099 a0001c0002t0010g0306 a0001c0002t0010g0315 |
3 | HG03491.hp2 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2259+406G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531866 | |||||||
| chr10:94531867 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+407T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531867 | |||||||
| chr10:94531871 | G | T | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+411G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531871 | |||||||
| chr10:94531872 | T | TTATTTTA | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+415_2259+416i others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531872 | ||||||
| chr10:94531911 | T | G | 60 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(57): Show |
60 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2259+451T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531911 | |||||||
| chr10:94531949 | C | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2259+489C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531949 | |||||||
| chr10:94532042 | G | A | 4 | a0001c0002t0003g0174 a0001c0002t0003g0175 a0001c0002t0003g0180 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+582G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532042 | |||||||
| chr10:94532125 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2259+665T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532125 | |||||||
| chr10:94532170 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2259+710G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532170 | |||||||
| chr10:94532217 | G | A | 4 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+757G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532217 | |||||||
| chr10:94532344 | A | AT | 14 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.2260-678dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94532344 | ||||||
| chr10:94532345 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2260-683T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532345 | |||||||
| chr10:94532471 | T | C | 15 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(12): Show |
15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2260-557T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532471 | |||||||
| chr10:94532519 | G | A | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2260-509G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532519 | |||||||
| chr10:94532890 | G | A | 7 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | HG02071.hp1 NA18942.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.2260-138G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532890 | |||||||
| chr10:94532894 | T | A | 11 | a0001c0001t0005g0200 a0001c0001t0005g0201 a0001c0001t0005g0202 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2260-134T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532894 |