Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 414060 |
| ensemblid | ENSG00000278299.6 |
| hgncid | 24889 |
| symbol | TBC1D3C |
| name | TBC1 domain family member 3C |
| refseq_nuc | NM_001001418.6 |
| refseq_prot | NP_001001418.5 |
| ensembl_nuc | ENST00000622206.2 |
| ensembl_prot | ENSP00000482345.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 38057693 |
| end | 38068634 |
| strand | - |
| ver | v1.2 |
| region | chr17:38057693-38068634 |
| region5000 | chr17:38052693-38073634 |
| regionname0 | TBC1D3C_chr17_38057693_38068634 |
| regionname5000 | TBC1D3C_chr17_38052693_38073634 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 549 | 29 | 6 | 3 | 18 | 0 | 2 | 16 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0002 | 0/0 | 549 | 24 | 10 | 3 | 7 | 2 | 2 | 7 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0003 | 0/0 | 549 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0004 | 0/0 | 549 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0005 | 0/0 | 549 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0006 | 0/0 | 549 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0007 | 0/0 | 549 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0008 | 0/0 | 549 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0009 | 0/0 | 549 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0010 | 0/0 | 549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0011 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0012 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0013 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0014 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0015 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0016 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0017 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0018 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0019 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| a0020 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | MDVVE others(544): Show |
chr17 | 38052693 | 38073634 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1647 | 27 | 5 | 2 | 18 | 0 | 2 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0001c0020 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0001c0024 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0002c0002 | 0/0 | 1647 | 14 | 2 | 3 | 6 | 1 | 2 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0002c0004 | 0/0 | 1647 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0002c0006 | 0/0 | 1647 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0002c0018 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0002c0022 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0002c0025 | 0/0 | 1647 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0003c0005 | 0/0 | 1647 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0003c0008 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0004c0003 | 0/0 | 1647 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0005c0009 | 0/0 | 1647 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0006c0010 | 0/0 | 1647 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0007c0007 | 0/0 | 1647 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0008c0012 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0009c0011 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0010c0023 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0011c0028 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0012c0015 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0013c0026 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0014c0013 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0015c0014 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0016c0016 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0017c0027 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0018c0017 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0019c0019 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 | ||
| a0020c0021 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | ATGGA others(1642): Show |
chr17 | 38052693 | 38073634 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2104 | 23 | 2 | 2 | 17 | 0 | 2 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0001c0001t0003 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0001c0001t0005 | 0/0 | 2104 | 3 | 2 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0001c0020t0001 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0001c0024t0002 | 0/0 | 2104 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0002t0002 | 0/0 | 2104 | 14 | 2 | 3 | 6 | 1 | 2 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0004t0004 | 0/0 | 2104 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0006t0003 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0006t0008 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0018t0003 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0022t0002 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0002c0025t0002 | 0/0 | 2104 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0003c0005t0001 | 0/0 | 2104 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0003c0008t0001 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0004c0003t0001 | 0/0 | 2104 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0005c0009t0001 | 0/0 | 2104 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0006c0010t0007 | 0/0 | 2104 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0007c0007t0006 | 0/0 | 2104 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0008c0012t0003 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0009c0011t0002 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0010c0023t0002 | 0/0 | 2104 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0011c0028t0003 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0012c0015t0009 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0013c0026t0002 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0014c0013t0011 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0015c0014t0001 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0016c0016t0010 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0017c0027t0002 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0018c0017t0001 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0019c0019t0001 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| a0020c0021t0002 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | AGCAC others(2099): Show |
chr17 | 38052693 | 38073634 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0020t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0001c0024t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0004t0004g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0006t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0006t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0006t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0018t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0022t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0002c0025t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0003c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0003c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0003c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0003c0008t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0003c0008t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0004c0003t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0004c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0004c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0004c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0005c0009t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0005c0009t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0006c0010t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0006c0010t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0007c0007t0006g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0008c0012t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0008c0012t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0009c0011t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0009c0011t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0010c0023t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0011c0028t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0012c0015t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0013c0026t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0014c0013t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0015c0014t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0016c0016t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0017c0027t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0018c0017t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0019c0019t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| a0020c0021t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG00544 | hp2 | a0005 | c0009 | t0001 | g0035 | EAS | CHS | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG00738 | hp1 | a0010 | c0023 | t0002 | g0011 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01109 | hp1 | a0001 | c0024 | t0002 | g0020 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01109 | hp2 | a0006 | c0010 | t0007 | g0073 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01168 | hp1 | a0007 | c0007 | t0006 | g0003 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01169 | hp1 | a0007 | c0007 | t0006 | g0003 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG01516 | hp2 | a0002 | c0025 | t0002 | g0014 | EUR | IBS | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02129 | hp2 | a0005 | c0009 | t0001 | g0036 | EAS | KHV | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02572 | hp1 | a0002 | c0004 | t0004 | g0002 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02572 | hp2 | a0004 | c0003 | t0001 | g0049 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02647 | hp1 | a0002 | c0006 | t0003 | g0055 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02647 | hp2 | a0006 | c0010 | t0007 | g0072 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02717 | hp1 | a0004 | c0003 | t0001 | g0050 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02809 | hp1 | a0011 | c0028 | t0003 | g0067 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02809 | hp2 | a0008 | c0012 | t0003 | g0048 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02818 | hp1 | a0003 | c0008 | t0001 | g0029 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02886 | hp1 | a0003 | c0005 | t0001 | g0032 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02886 | hp2 | a0004 | c0003 | t0001 | g0004 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02895 | hp1 | a0012 | c0015 | t0009 | g0070 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02897 | hp1 | a0001 | c0020 | t0001 | g0056 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02922 | hp1 | a0004 | c0003 | t0001 | g0033 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02922 | hp2 | a0003 | c0005 | t0001 | g0071 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02970 | hp1 | a0013 | c0026 | t0002 | g0015 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03139 | hp1 | a0002 | c0004 | t0004 | g0002 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03195 | hp1 | a0002 | c0006 | t0008 | g0028 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03195 | hp2 | a0009 | c0011 | t0002 | g0010 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03486 | hp1 | a0014 | c0013 | t0011 | g0068 | AFR | MSL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03486 | hp2 | a0015 | c0014 | t0001 | g0046 | AFR | MSL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03516 | hp1 | a0002 | c0004 | t0004 | g0002 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03540 | hp1 | a0003 | c0005 | t0001 | g0045 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03540 | hp2 | a0016 | c0016 | t0010 | g0051 | AFR | GWD | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03579 | hp1 | a0003 | c0008 | t0001 | g0030 | AFR | MSL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG03579 | hp2 | a0008 | c0012 | t0003 | g0034 | AFR | MSL | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18946 | hp1 | a0017 | c0027 | t0002 | g0024 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18946 | hp2 | a0018 | c0017 | t0001 | g0057 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19007 | hp2 | a0002 | c0018 | t0003 | g0039 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19079 | hp1 | a0019 | c0019 | t0001 | g0059 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02559 | hp1 | a0002 | c0006 | t0003 | g0052 | AFR | ACB | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG02559 | hp2 | a0002 | c0004 | t0004 | g0002 | AFR | ACB | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG06807 | hp1 | a0004 | c0003 | t0001 | g0004 | AFR | USA | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| HG06807 | hp2 | a0002 | c0022 | t0002 | g0019 | AFR | USA | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA21309 | hp1 | a0020 | c0021 | t0002 | g0021 | AFR | LWK | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| NA21309 | hp2 | a0009 | c0011 | t0002 | g0022 | AFR | LWK | TBC1D3C_chr17_38052693_38073634 | TBC1D3C | chr17 | 38052693 | 38073634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38058035 | T | A | 2 | a0006 a0012 |
3 | HG01109.hp2 HG02647.hp2 HG02895.hp1 |
missense_variant | MODERATE | c.1623A>T | p.Glu541Asp | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1763/2105 | 1623/1650 | 541/549 | chr17 | 38058035 | |||
| chr17:38058081 | T | G | 3 | a0009 a0019 a0020 |
4 | HG03195.hp2 NA19079.hp1 NA21309.hp1 others(1): Show |
missense_variant | MODERATE | c.1577A>C | p.Gln526Pro | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1717/2105 | 1577/1650 | 526/549 | chr17 | 38058081 | |||
| chr17:38058169 | G | A | 1 | a0016 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1489C>T | p.His497Tyr | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1629/2105 | 1489/1650 | 497/549 | chr17 | 38058169 | |||
| chr17:38058207 | G | T | 1 | a0010 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1451C>A | p.Ser484Tyr | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1591/2105 | 1451/1650 | 484/549 | chr17 | 38058207 | |||
| chr17:38058216 | C | T | 1 | a0015 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1442G>A | p.Arg481His | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1582/2105 | 1442/1650 | 481/549 | chr17 | 38058216 | |||
| chr17:38058219 | A | G | 1 | a0010 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1439T>C | p.Val480Ala | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1579/2105 | 1439/1650 | 480/549 | chr17 | 38058219 | |||
| chr17:38058441 | G | A | 1 | a0010 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1217C>T | p.Pro406Leu | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1357/2105 | 1217/1650 | 406/549 | chr17 | 38058441 | |||
| chr17:38059579 | T | G | 8 | a0001 a0004 a0005 others(5): Show |
42 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(39): Show |
missense_variant | MODERATE | c.1060A>C | p.Lys354Gln | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/14 | 1200/2105 | 1060/1650 | 354/549 | chr17 | 38059579 | |||
| chr17:38060129 | C | T | 1 | a0014 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.880G>A | p.Glu294Lys | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/14 | 1020/2105 | 880/1650 | 294/549 | chr17 | 38060129 | |||
| chr17:38060660 | C | T | 1 | a0020 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.812G>A | p.Arg271Gln | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/14 | 952/2105 | 812/1650 | 271/549 | chr17 | 38060660 | |||
| chr17:38061987 | C | T | 1 | a0005 | 2 | HG00544.hp2 HG02129.hp2 |
missense_variant | MODERATE | c.583G>A | p.Ala195Thr | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/14 | 723/2105 | 583/1650 | 195/549 | chr17 | 38061987 | |||
| chr17:38063897 | T | C | 1 | a0014 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.471A>G | p.Ile157Met | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/14 | 611/2105 | 471/1650 | 157/549 | chr17 | 38063897 | |||
| chr17:38063923 | C | T | 1 | a0014 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.445G>A | p.Val149Ile | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/14 | 585/2105 | 445/1650 | 149/549 | chr17 | 38063923 | |||
| chr17:38063958 | C | T | 2 | a0007 a0018 |
3 | HG01168.hp1 HG01169.hp1 NA18946.hp2 |
missense_variant | MODERATE | c.410G>A | p.Arg137Lys | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/14 | 550/2105 | 410/1650 | 137/549 | chr17 | 38063958 | |||
| chr17:38064347 | G | A | 12 | a0001 a0002 a0005 others(9): Show |
67 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(64): Show |
missense_variant | MODERATE | c.350C>T | p.Thr117Ile | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 6/14 | 490/2105 | 350/1650 | 117/549 | chr17 | 38064347 | |||
| chr17:38064371 | G | A | 1 | a0008 | 2 | HG02809.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.326C>T | p.Pro109Leu | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 6/14 | 466/2105 | 326/1650 | 109/549 | chr17 | 38064371 | |||
| chr17:38065435 | G | A | 1 | a0013 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.187C>T | p.Arg63Trp | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 4/14 | 327/2105 | 187/1650 | 63/549 | chr17 | 38065435 | |||
| chr17:38066762 | T | C | 1 | a0017 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.143A>G | p.His48Arg | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/14 | 283/2105 | 143/1650 | 48/549 | chr17 | 38066762 | |||
| chr17:38067018 | C | G | 1 | a0011 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.49G>C | p.Asp17His | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 2/14 | 189/2105 | 49/1650 | 17/549 | chr17 | 38067018 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38058233 | T | C | 1 | a0002c0022 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1425A>G | p.Arg475Arg | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1565/2105 | 1425/1650 | 475/549 | chr17 | 38058233 | |||
| chr17:38058260 | G | C | 1 | a0003c0008 | 2 | HG02818.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.1398C>G | p.Gly466Gly | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 1538/2105 | 1398/1650 | 466/549 | chr17 | 38058260 | |||
| chr17:38059655 | G | A | 1 | a0002c0025 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.984C>T | p.Phe328Phe | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/14 | 1124/2105 | 984/1650 | 328/549 | chr17 | 38059655 | |||
| chr17:38060120 | A | G | 4 | a0002c0004 a0002c0006 a0002c0018 others(1): Show |
10 | HG01168.hp1 HG01169.hp1 HG02559.hp1 others(7): Show |
synonymous_variant | LOW | c.889T>C | p.Leu297Leu | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/14 | 1029/2105 | 889/1650 | 297/549 | chr17 | 38060120 | |||
| chr17:38061910 | G | A | 1 | a0003c0008 | 2 | HG02818.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.660C>T | p.Ser220Ser | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/14 | 800/2105 | 660/1650 | 220/549 | chr17 | 38061910 | |||
| chr17:38062573 | G | A | 12 | a0001c0024 a0002c0002 a0002c0022 others(9): Show |
27 | HG00738.hp1 HG01109.hp1 HG01168.hp2 others(24): Show |
synonymous_variant | LOW | c.540C>T | p.Tyr180Tyr | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/14 | 680/2105 | 540/1650 | 180/549 | chr17 | 38062573 | |||
| chr17:38063911 | A | G | 4 | a0001c0001 a0002c0018 a0005c0009 others(1): Show |
31 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(28): Show |
synonymous_variant | LOW | c.457T>C | p.Leu153Leu | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/14 | 597/2105 | 457/1650 | 153/549 | chr17 | 38063911 | |||
| chr17:38064876 | G | A | 1 | a0002c0004 | 4 | HG02559.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.264C>T | p.Tyr88Tyr | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 5/14 | 404/2105 | 264/1650 | 88/549 | chr17 | 38064876 | |||
| chr17:38067043 | G | A | 1 | a0011c0028 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.24C>T | p.Gly8Gly | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 2/14 | 164/2105 | 24/1650 | 8/549 | chr17 | 38067043 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38057764 | T | C | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
78 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 244 | chr17 | 38057764 | ||||||
| chr17:38057819 | G | C | 1 | a0016c0016t0010 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 189 | chr17 | 38057819 | ||||||
| chr17:38057827 | T | C | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0020t0001 others(7): Show |
42 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 181 | chr17 | 38057827 | ||||||
| chr17:38057935 | C | T | 2 | a0006c0010t0007 a0012c0015t0009 |
3 | HG01109.hp2 HG02647.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*73G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 73 | chr17 | 38057935 | ||||||
| chr17:38057941 | T | C | 1 | a0014c0013t0011 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*67A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 14/14 | 67 | chr17 | 38057941 | ||||||
| chr17:38068526 | G | A | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
79 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(76): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/14 | chr17 | 38068526 | |||||||
| chr17:38068588 | G | A | 1 | a0006c0010t0007 | 2 | HG01109.hp2 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-94C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/14 | 1522 | chr17 | 38068588 | ||||||
| chr17:38068609 | G | C | 1 | a0001c0001t0005 | 3 | HG02717.hp2 HG02818.hp2 NA19065.hp2 |
5_prime_UTR_variant | MODIFIER | c.-115C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/14 | 1543 | chr17 | 38068609 | ||||||
| chr17:38068614 | A | G | 10 | a0001c0001t0005 a0001c0024t0002 a0002c0002t0002 others(7): Show |
26 | HG00738.hp1 HG01109.hp1 HG01168.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-120T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/14 | 1548 | chr17 | 38068614 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38058744 | G | A | 6 | a0001c0001t0005g0026 a0003c0005t0001g0032 a0004c0003t0001g0004 others(3): Show |
7 | HG00738.hp1 HG02572.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1082-168C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38058744 | |||||||
| chr17:38058823 | G | A | 1 | a0017c0027t0002g0024 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1082-247C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38058823 | |||||||
| chr17:38058920 | C | T | 1 | a0001c0024t0002g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1082-344G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38058920 | |||||||
| chr17:38058986 | G | A | 1 | a0004c0003t0001g0004 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1082-410C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38058986 | |||||||
| chr17:38059060 | GGCCCGGG others(11): Show |
G | 8 | a0001c0001t0001g0061 a0002c0004t0004g0002 a0008c0012t0003g0034 others(5): Show |
11 | HG02559.hp2 HG02572.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081+480_1082-485d others(20): Show |
TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38059060 | |||||||
| chr17:38059111 | C | T | 1 | a0020c0021t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1081+447G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38059111 | |||||||
| chr17:38059367 | C | T | 3 | a0001c0001t0005g0026 a0004c0003t0001g0004 a0004c0003t0001g0049 |
4 | HG02572.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+191G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38059367 | |||||||
| chr17:38059402 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1081+156C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38059402 | |||||||
| chr17:38059548 | T | C | 1 | a0001c0001t0005g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+10A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 13/13 | chr17 | 38059548 | |||||||
| chr17:38059772 | C | A | 6 | a0003c0005t0001g0045 a0006c0010t0007g0072 a0006c0010t0007g0073 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.929-62G>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/13 | chr17 | 38059772 | |||||||
| chr17:38059799 | G | A | 1 | a0010c0023t0002g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.929-89C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/13 | chr17 | 38059799 | |||||||
| chr17:38059839 | C | T | 15 | a0001c0001t0005g0026 a0002c0006t0003g0052 a0002c0006t0003g0055 others(12): Show |
16 | HG01109.hp2 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.929-129G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/13 | chr17 | 38059839 | |||||||
| chr17:38059963 | A | G | 1 | a0011c0028t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928+118T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/13 | chr17 | 38059963 | |||||||
| chr17:38060070 | C | T | 2 | a0006c0010t0007g0072 a0006c0010t0007g0073 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.928+11G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 12/13 | chr17 | 38060070 | |||||||
| chr17:38060312 | C | T | 1 | a0001c0001t0005g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.829-132G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060312 | |||||||
| chr17:38060336 | G | A | 2 | a0003c0005t0001g0045 a0015c0014t0001g0046 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.829-156C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060336 | |||||||
| chr17:38060357 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(27): Show |
32 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.829-177A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060357 | |||||||
| chr17:38060409 | T | C | 1 | a0010c0023t0002g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.829-229A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060409 | |||||||
| chr17:38060516 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(69): Show |
80 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.828+128G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060516 | |||||||
| chr17:38060536 | G | A | 1 | a0003c0008t0001g0030 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.828+108C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060536 | |||||||
| chr17:38060536 | G | T | 2 | a0003c0005t0001g0045 a0015c0014t0001g0046 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.828+108C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 11/13 | chr17 | 38060536 | |||||||
| chr17:38060729 | T | G | 2 | a0003c0005t0001g0045 a0015c0014t0001g0046 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.763-20A>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 10/13 | chr17 | 38060729 | |||||||
| chr17:38060783 | C | G | 2 | a0008c0012t0003g0034 a0008c0012t0003g0048 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.763-74G>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 10/13 | chr17 | 38060783 | |||||||
| chr17:38060854 | G | A | 1 | a0002c0006t0008g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.763-145C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 10/13 | chr17 | 38060854 | |||||||
| chr17:38060884 | C | T | 19 | a0001c0024t0002g0020 a0002c0002t0002g0001 a0002c0002t0002g0007 others(16): Show |
23 | HG01109.hp1 HG01168.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.763-175G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 10/13 | chr17 | 38060884 | |||||||
| chr17:38060978 | A | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(28): Show |
34 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.762+117T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 10/13 | chr17 | 38060978 | |||||||
| chr17:38060981 | C | A | 20 | a0001c0024t0002g0020 a0002c0002t0002g0001 a0002c0002t0002g0007 others(17): Show |
24 | HG01109.hp1 HG01168.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.762+114G>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 10/13 | chr17 | 38060981 | |||||||
| chr17:38061306 | G | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0038 others(62): Show |
72 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.668-117C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061306 | |||||||
| chr17:38061461 | G | A | 5 | a0003c0005t0001g0045 a0003c0005t0001g0071 a0008c0012t0003g0034 others(2): Show |
5 | HG02809.hp2 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.668-272C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061461 | |||||||
| chr17:38061505 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(51): Show |
61 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.668-316T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061505 | |||||||
| chr17:38061552 | A | G | 8 | a0003c0005t0001g0032 a0004c0003t0001g0050 a0006c0010t0007g0072 others(5): Show |
8 | HG01109.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.667+351T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061552 | |||||||
| chr17:38061577 | A | G | 2 | a0003c0008t0001g0029 a0003c0008t0001g0030 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.667+326T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061577 | |||||||
| chr17:38061635 | A | G | 4 | a0003c0005t0001g0045 a0008c0012t0003g0034 a0008c0012t0003g0048 others(1): Show |
4 | HG02809.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+268T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061635 | |||||||
| chr17:38061644 | G | A | 2 | a0002c0002t0002g0009 a0002c0002t0002g0012 |
2 | HG01168.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.667+259C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061644 | |||||||
| chr17:38061691 | A | G | 2 | a0005c0009t0001g0035 a0012c0015t0009g0070 |
2 | HG00544.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.667+212T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061691 | |||||||
| chr17:38061714 | G | C | 32 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0043 others(29): Show |
40 | HG00544.hp1 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.667+189C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061714 | |||||||
| chr17:38061716 | G | A | 2 | a0006c0010t0007g0072 a0006c0010t0007g0073 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.667+187C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061716 | |||||||
| chr17:38061718 | C | G | 2 | a0006c0010t0007g0072 a0006c0010t0007g0073 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.667+185G>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061718 | |||||||
| chr17:38061719 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0064 others(1): Show |
4 | HG00738.hp2 HG01169.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+184C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061719 | |||||||
| chr17:38061744 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0038 others(11): Show |
16 | HG01109.hp2 HG01169.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.667+159G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061744 | |||||||
| chr17:38061778 | C | T | 3 | a0004c0003t0001g0049 a0004c0003t0001g0050 a0010c0023t0002g0011 |
3 | HG00738.hp1 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.667+125G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061778 | |||||||
| chr17:38061841 | T | C | 3 | a0006c0010t0007g0073 a0011c0028t0003g0067 a0012c0015t0009g0070 |
3 | HG01109.hp2 HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.667+62A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061841 | |||||||
| chr17:38061863 | G | A | 2 | a0003c0008t0001g0029 a0003c0008t0001g0030 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.667+40C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 9/13 | chr17 | 38061863 | |||||||
| chr17:38062079 | T | C | 1 | a0003c0005t0001g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.547-56A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/13 | chr17 | 38062079 | |||||||
| chr17:38062372 | T | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0054 a0001c0001t0005g0025 others(5): Show |
8 | HG02559.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+195A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/13 | chr17 | 38062372 | |||||||
| chr17:38062402 | C | T | 3 | a0006c0010t0007g0072 a0006c0010t0007g0073 a0012c0015t0009g0070 |
3 | HG01109.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.546+165G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/13 | chr17 | 38062402 | |||||||
| chr17:38062479 | T | G | 4 | a0002c0006t0003g0052 a0003c0005t0001g0032 a0004c0003t0001g0033 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+88A>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/13 | chr17 | 38062479 | |||||||
| chr17:38062539 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.546+28G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/13 | chr17 | 38062539 | |||||||
| chr17:38062566 | C | G | 3 | a0001c0001t0001g0037 a0005c0009t0001g0035 a0005c0009t0001g0036 |
3 | HG00544.hp2 HG02129.hp2 NA18968.hp1 |
splice_donor_variant&intron_variant | HIGH | c.546+1G>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 8/13 | chr17 | 38062566 | |||||||
| chr17:38062625 | A | C | 1 | a0002c0002t0002g0018 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.498-10T>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062625 | |||||||
| chr17:38062716 | T | G | 3 | a0006c0010t0007g0072 a0006c0010t0007g0073 a0012c0015t0009g0070 |
3 | HG01109.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.498-101A>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062716 | |||||||
| chr17:38062757 | T | C | 5 | a0001c0001t0001g0065 a0007c0007t0006g0003 a0010c0023t0002g0011 others(2): Show |
6 | HG00544.hp1 HG00738.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-142A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062757 | |||||||
| chr17:38062816 | A | G | 2 | a0008c0012t0003g0034 a0008c0012t0003g0048 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.498-201T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062816 | |||||||
| chr17:38062848 | AT | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0040 others(35): Show |
40 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.498-234delA | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062848 | |||||||
| chr17:38062848 | ATT | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0024t0002g0020 others(19): Show |
27 | HG01109.hp1 HG01168.hp2 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.498-235_498-234del others(2): Show |
TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062848 | |||||||
| chr17:38062913 | C | T | 2 | a0002c0002t0002g0017 a0003c0005t0001g0071 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.498-298G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062913 | |||||||
| chr17:38062925 | G | A | 9 | a0004c0003t0001g0004 a0004c0003t0001g0049 a0006c0010t0007g0072 others(6): Show |
11 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.498-310C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062925 | |||||||
| chr17:38062949 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.498-334C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38062949 | |||||||
| chr17:38063010 | C | A | 1 | a0014c0013t0011g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.498-395G>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063010 | |||||||
| chr17:38063040 | G | A | 3 | a0006c0010t0007g0072 a0006c0010t0007g0073 a0012c0015t0009g0070 |
3 | HG01109.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.498-425C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063040 | |||||||
| chr17:38063074 | G | C | 1 | a0014c0013t0011g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.498-459C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063074 | |||||||
| chr17:38063110 | T | G | 22 | a0001c0024t0002g0020 a0002c0002t0002g0001 a0002c0002t0002g0007 others(19): Show |
26 | HG00738.hp1 HG01109.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.498-495A>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063110 | |||||||
| chr17:38063428 | G | T | 1 | a0014c0013t0011g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497+443C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063428 | |||||||
| chr17:38063532 | G | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(41): Show |
48 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.497+339C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063532 | |||||||
| chr17:38063536 | G | C | 2 | a0009c0011t0002g0022 a0020c0021t0002g0021 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497+335C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063536 | |||||||
| chr17:38063568 | G | A | 1 | a0007c0007t0006g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.497+303C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063568 | |||||||
| chr17:38063618 | T | C | 3 | a0001c0001t0001g0037 a0005c0009t0001g0035 a0005c0009t0001g0036 |
3 | HG00544.hp2 HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.497+253A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063618 | |||||||
| chr17:38063628 | G | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(69): Show |
80 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.497+243C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 7/13 | chr17 | 38063628 | |||||||
| chr17:38064070 | C | T | 3 | a0006c0010t0007g0072 a0006c0010t0007g0073 a0012c0015t0009g0070 |
3 | HG01109.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.388-90G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 6/13 | chr17 | 38064070 | |||||||
| chr17:38064453 | G | A | 1 | a0002c0002t0002g0001 | 2 | HG01358.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.280-36C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 5/13 | chr17 | 38064453 | |||||||
| chr17:38064630 | A | C | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0016 others(1): Show |
4 | HG01516.hp1 HG02698.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-213T>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 5/13 | chr17 | 38064630 | |||||||
| chr17:38064994 | G | A | 1 | a0003c0005t0001g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.199-53C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 4/13 | chr17 | 38064994 | |||||||
| chr17:38065243 | T | C | 1 | a0012c0015t0009g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.198+181A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 4/13 | chr17 | 38065243 | |||||||
| chr17:38065315 | G | T | 1 | a0011c0028t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.198+109C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 4/13 | chr17 | 38065315 | |||||||
| chr17:38065386 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.198+38G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 4/13 | chr17 | 38065386 | |||||||
| chr17:38065503 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.159-40C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065503 | |||||||
| chr17:38065529 | C | T | 2 | a0004c0003t0001g0004 a0004c0003t0001g0049 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.159-66G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065529 | |||||||
| chr17:38065569 | G | A | 1 | a0016c0016t0010g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159-106C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065569 | |||||||
| chr17:38065647 | C | G | 1 | a0016c0016t0010g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159-184G>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065647 | |||||||
| chr17:38065701 | C | A | 1 | a0004c0003t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.159-238G>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065701 | |||||||
| chr17:38065737 | G | C | 2 | a0009c0011t0002g0022 a0020c0021t0002g0021 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.159-274C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065737 | |||||||
| chr17:38065864 | G | A | 1 | a0014c0013t0011g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.159-401C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065864 | |||||||
| chr17:38065936 | A | G | 1 | a0014c0013t0011g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.159-473T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065936 | |||||||
| chr17:38065956 | G | A | 1 | a0011c0028t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.159-493C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065956 | |||||||
| chr17:38065998 | A | G | 3 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0013c0026t0002g0015 |
3 | HG01516.hp1 HG02698.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.159-535T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38065998 | |||||||
| chr17:38066008 | C | T | 2 | a0006c0010t0007g0072 a0006c0010t0007g0073 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.159-545G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066008 | |||||||
| chr17:38066011 | G | A | 1 | a0002c0002t0002g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.159-548C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066011 | |||||||
| chr17:38066015 | T | G | 1 | a0014c0013t0011g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.159-552A>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066015 | |||||||
| chr17:38066034 | G | T | 2 | a0006c0010t0007g0072 a0006c0010t0007g0073 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.159-571C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066034 | |||||||
| chr17:38066169 | C | T | 2 | a0002c0002t0002g0008 a0013c0026t0002g0015 |
2 | HG01516.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.158+578G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066169 | |||||||
| chr17:38066232 | CT | C | 2 | a0006c0010t0007g0072 a0006c0010t0007g0073 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.158+514delA | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066232 | |||||||
| chr17:38066301 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0060 others(4): Show |
8 | HG00738.hp2 HG01169.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.158+446G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066301 | |||||||
| chr17:38066385 | C | A | 3 | a0001c0001t0001g0037 a0005c0009t0001g0035 a0005c0009t0001g0036 |
3 | HG00544.hp2 HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.158+362G>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066385 | |||||||
| chr17:38066389 | T | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(69): Show |
82 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.158+358A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066389 | |||||||
| chr17:38066424 | G | A | 2 | a0004c0003t0001g0004 a0004c0003t0001g0049 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.158+323C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066424 | |||||||
| chr17:38066427 | G | T | 3 | a0001c0001t0001g0037 a0005c0009t0001g0035 a0005c0009t0001g0036 |
3 | HG00544.hp2 HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.158+320C>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066427 | |||||||
| chr17:38066557 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0058 others(8): Show |
13 | HG00738.hp2 HG01169.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.158+190C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066557 | |||||||
| chr17:38066585 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG03017.hp2 NA18943.hp1 NA19011.hp1 others(4): Show |
intron_variant | MODIFIER | c.158+162C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 3/13 | chr17 | 38066585 | |||||||
| chr17:38067098 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(44): Show |
49 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-31G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067098 | |||||||
| chr17:38067105 | G | C | 1 | a0002c0006t0003g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1-38C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067105 | |||||||
| chr17:38067136 | G | A | 2 | a0004c0003t0001g0004 a0004c0003t0001g0049 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-1-69C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067136 | |||||||
| chr17:38067139 | G | A | 2 | a0003c0005t0001g0045 a0015c0014t0001g0046 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-72C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067139 | |||||||
| chr17:38067266 | A | G | 5 | a0002c0004t0004g0002 a0002c0006t0003g0052 a0008c0012t0003g0034 others(2): Show |
8 | HG02559.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-199T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067266 | |||||||
| chr17:38067480 | C | G | 1 | a0011c0028t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-413G>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067480 | |||||||
| chr17:38067485 | C | A | 1 | a0011c0028t0003g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-418G>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067485 | |||||||
| chr17:38067632 | G | A | 3 | a0003c0005t0001g0032 a0004c0003t0001g0033 a0011c0028t0003g0067 |
3 | HG02809.hp1 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-1-565C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067632 | |||||||
| chr17:38067634 | G | GA | 2 | a0004c0003t0001g0004 a0004c0003t0001g0049 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-1-568dupT | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067634 | |||||||
| chr17:38067640 | A | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0037 others(39): Show |
44 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-1-573T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067640 | |||||||
| chr17:38067791 | C | T | 1 | a0004c0003t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-2+705G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067791 | |||||||
| chr17:38067832 | C | T | 2 | a0003c0005t0001g0032 a0004c0003t0001g0033 |
2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-2+664G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067832 | |||||||
| chr17:38067864 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-2+632C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067864 | |||||||
| chr17:38067871 | A | G | 3 | a0002c0006t0008g0028 a0006c0010t0007g0072 a0006c0010t0007g0073 |
3 | HG01109.hp2 HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+625T>C | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067871 | |||||||
| chr17:38067890 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-2+606A>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067890 | |||||||
| chr17:38067936 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-2+560G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067936 | |||||||
| chr17:38067953 | G | C | 1 | a0001c0001t0005g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2+543C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067953 | |||||||
| chr17:38067956 | GCCCAAGG others(11): Show |
G | 2 | a0004c0003t0001g0004 a0004c0003t0001g0049 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-2+522_-2+539delGA others(16): Show |
TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38067956 | |||||||
| chr17:38068024 | G | C | 1 | a0008c0012t0003g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-2+472C>G | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38068024 | |||||||
| chr17:38068072 | GTACCAGT others(7): Show |
G | 19 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(16): Show |
19 | HG00544.hp2 HG02129.hp2 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2+410_-2+423delTA others(12): Show |
TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38068072 | |||||||
| chr17:38068154 | TAGGGC | T | 2 | a0003c0008t0001g0029 a0003c0008t0001g0030 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+337_-2+341delGC others(3): Show |
TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38068154 | |||||||
| chr17:38068287 | G | A | 2 | a0003c0005t0001g0071 a0012c0015t0009g0070 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2+209C>T | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38068287 | |||||||
| chr17:38068337 | C | T | 1 | a0002c0002t0002g0007 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-2+159G>A | TBC1D3C | ENSG00000278299.6 | transcript | ENST00000622206.2 | protein_coding | 1/13 | chr17 | 38068337 |