Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55357 |
| ensemblid | ENSG00000095383.20 |
| hgncid | 18026 |
| symbol | TBC1D2 |
| name | TBC1 domain family member 2 |
| refseq_nuc | NM_001267571.2 |
| refseq_prot | NP_001254500.1 |
| ensembl_nuc | ENST00000465784.7 |
| ensembl_prot | ENSP00000481721.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 98199011 |
| end | 98255649 |
| strand | - |
| ver | v1.2 |
| region | chr9:98199011-98255649 |
| region5000 | chr9:98194011-98260649 |
| regionname0 | TBC1D2_chr9_98199011_98255649 |
| regionname5000 | TBC1D2_chr9_98194011_98260649 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 928 | 197 | 16 | 42 | 105 | 9 | 23 | 87 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0002 | 0/0 | 928 | 74 | 10 | 15 | 38 | 3 | 8 | 32 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0003 | 0/0 | 928 | 55 | 40 | 9 | 3 | 2 | 1 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0004 | 0/0 | 928 | 8 | 3 | 2 | 0 | 2 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0005 | 0/0 | 928 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0006 | 0/0 | 928 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0007 | 0/0 | 928 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0008 | 0/0 | 25 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MSAVL others(20): Show |
chr9 | 98194011 | 98260649 |
| a0009 | 0/0 | 928 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0010 | 0/0 | 928 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0011 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0012 | 0/0 | 928 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0013 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0014 | 0/0 | 928 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0015 | 0/0 | 928 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0016 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0017 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0018 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0019 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0020 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0021 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0022 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0023 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| a0024 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | MEGAG others(923): Show |
chr9 | 98194011 | 98260649 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2784 | 99 | 9 | 17 | 56 | 3 | 13 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0001c0002 | 1/0 | 2784 | 82 | 2 | 19 | 44 | 6 | 10 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0001c0006 | 0/0 | 2784 | 7 | 1 | 4 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0001c0008 | 0/0 | 2784 | 6 | 4 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0001c0019 | 0/0 | 2784 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0001c0039 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0002c0003 | 0/0 | 2784 | 65 | 3 | 13 | 38 | 3 | 8 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0002c0007 | 0/0 | 2784 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0002c0014 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0002c0030 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0004 | 0/0 | 2784 | 42 | 29 | 7 | 3 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0009 | 0/0 | 2784 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0011 | 0/0 | 2784 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0012 | 0/0 | 2784 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0026 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0034 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0003c0036 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0004c0005 | 0/0 | 2784 | 8 | 3 | 2 | 0 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0005c0010 | 0/0 | 2784 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0005c0015 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0006c0016 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0006c0035 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0006c0038 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0007c0018 | 0/0 | 2784 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0008c0020 | 0/0 | 2784 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GTGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0009c0013 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0010c0017 | 0/0 | 2784 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0011c0040 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0012c0032 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0013c0023 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0014c0031 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0015c0028 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0016c0025 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0017c0024 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0018c0029 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0019c0021 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0020c0037 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0021c0027 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0022c0041 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0023c0033 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 | ||
| a0024c0022 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | ATGGA others(2779): Show |
chr9 | 98194011 | 98260649 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3265 | 99 | 9 | 17 | 56 | 3 | 13 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0001c0002t0001 | 1/0 | 3265 | 81 | 2 | 19 | 43 | 6 | 10 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0001c0002t0002 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0001c0006t0001 | 0/0 | 3265 | 7 | 1 | 4 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0001c0008t0001 | 0/0 | 3265 | 6 | 4 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0001c0019t0001 | 0/0 | 3265 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0001c0039t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0002c0003t0001 | 0/0 | 3265 | 65 | 3 | 13 | 38 | 3 | 8 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0002c0007t0001 | 0/0 | 3265 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0002c0014t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0002c0030t0001 | 0/0 | 3265 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0004t0001 | 0/0 | 3265 | 41 | 28 | 7 | 3 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0004t0003 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0009t0001 | 0/0 | 3265 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0011t0001 | 0/0 | 3265 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0012t0001 | 0/0 | 3265 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0026t0001 | 0/0 | 3265 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0034t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0003c0036t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0004c0005t0001 | 0/0 | 3265 | 8 | 3 | 2 | 0 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0005c0010t0001 | 0/0 | 3265 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0005c0015t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0006c0016t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0006c0035t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0006c0038t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0007c0018t0001 | 0/0 | 3265 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0008c0020t0001 | 0/0 | 3265 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0009c0013t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0010c0017t0001 | 0/0 | 3265 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0011c0040t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0012c0032t0001 | 0/0 | 3265 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0013c0023t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0014c0031t0001 | 0/0 | 3265 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0015c0028t0001 | 0/0 | 3265 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0016c0025t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0017c0024t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0018c0029t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0019c0021t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0020c0037t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0021c0027t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0022c0041t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0023c0033t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| a0024c0022t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | GCCCC others(3260): Show |
chr9 | 98194011 | 98260649 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0001 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0003 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0004 | 1/0 | 4 | 0 | 1 | 0 | 0 | 2 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0006t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0006t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0006t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0006t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0006t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0008t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0008t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0008t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0019t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0019t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0001c0039t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0006 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0007t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0007t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0007t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0014t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0002c0030t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0004t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0009t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0009t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0009t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0011t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0011t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0011t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0012t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0012t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0012t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0026t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0034t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0003c0036t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0004c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0005c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0005c0010t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0005c0010t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0005c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0005c0015t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0005c0015t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0006c0016t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0006c0016t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0006c0035t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0006c0038t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0007c0018t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0007c0018t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0008c0020t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0008c0020t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0009c0013t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0009c0013t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0010c0017t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0010c0017t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0011c0040t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0012c0032t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0013c0023t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0014c0031t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0015c0028t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0016c0025t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0017c0024t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0018c0029t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0019c0021t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0020c0037t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0021c0027t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0022c0041t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0023c0033t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| a0024c0022t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0005 | t0001 | g0267 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0166 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0017 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00140 | hp2 | a0004 | c0005 | t0001 | g0082 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00280 | hp1 | a0003 | c0004 | t0001 | g0298 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00323 | hp1 | a0003 | c0004 | t0001 | g0295 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0236 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0285 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0231 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00544 | hp1 | a0001 | c0039 | t0001 | g0062 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00597 | hp2 | a0011 | c0040 | t0001 | g0143 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0216 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0240 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0293 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00733 | hp1 | a0004 | c0005 | t0001 | g0266 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0239 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00738 | hp1 | a0004 | c0005 | t0001 | g0265 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0244 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0243 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01071 | hp2 | a0007 | c0018 | t0001 | g0078 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01081 | hp1 | a0003 | c0004 | t0001 | g0048 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01081 | hp2 | a0001 | c0008 | t0001 | g0122 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0209 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01106 | hp1 | a0012 | c0032 | t0001 | g0223 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0287 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0288 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01169 | hp2 | a0003 | c0004 | t0001 | g0289 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0286 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01243 | hp2 | a0003 | c0026 | t0001 | g0044 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01255 | hp1 | a0001 | c0008 | t0001 | g0121 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01255 | hp2 | a0003 | c0009 | t0001 | g0036 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01346 | hp1 | a0001 | c0006 | t0001 | g0139 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0022 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0210 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01361 | hp2 | a0002 | c0030 | t0001 | g0241 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0250 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01496 | hp2 | a0002 | c0007 | t0001 | g0229 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0307 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0141 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0006 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0142 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0310 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01884 | hp2 | a0005 | c0015 | t0001 | g0034 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0101 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01891 | hp2 | a0003 | c0004 | t0003 | g0049 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0023 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01952 | hp2 | a0003 | c0004 | t0001 | g0296 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0232 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01993 | hp1 | a0001 | c0006 | t0001 | g0018 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0257 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02129 | hp1 | a0008 | c0020 | t0001 | g0318 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02129 | hp2 | a0003 | c0004 | t0001 | g0294 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02145 | hp1 | a0009 | c0013 | t0001 | g0029 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0234 | EAS | CDX | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02258 | hp1 | a0003 | c0004 | t0001 | g0275 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02258 | hp2 | a0002 | c0014 | t0001 | g0012 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02273 | hp2 | a0001 | c0006 | t0001 | g0154 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0299 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02280 | hp2 | a0013 | c0023 | t0001 | g0031 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02293 | hp2 | a0001 | c0006 | t0001 | g0162 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0022 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02451 | hp1 | a0003 | c0009 | t0001 | g0035 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0280 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0270 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02572 | hp2 | a0009 | c0013 | t0001 | g0028 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0235 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02615 | hp1 | a0003 | c0011 | t0001 | g0047 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02615 | hp2 | a0003 | c0004 | t0001 | g0283 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02622 | hp1 | a0004 | c0005 | t0001 | g0268 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02622 | hp2 | a0001 | c0008 | t0001 | g0123 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0260 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02630 | hp2 | a0005 | c0010 | t0001 | g0041 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02698 | hp1 | a0007 | c0018 | t0001 | g0079 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02698 | hp2 | a0014 | c0031 | t0001 | g0246 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02717 | hp2 | a0003 | c0012 | t0001 | g0271 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02723 | hp1 | a0002 | c0007 | t0001 | g0007 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0060 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02735 | hp1 | a0015 | c0028 | t0001 | g0233 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0208 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0255 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02738 | hp2 | a0003 | c0004 | t0001 | g0301 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02809 | hp1 | a0002 | c0007 | t0001 | g0007 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02818 | hp1 | a0005 | c0010 | t0001 | g0040 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02818 | hp2 | a0016 | c0025 | t0001 | g0042 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02895 | hp1 | a0006 | c0016 | t0001 | g0052 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02895 | hp2 | a0002 | c0007 | t0001 | g0007 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02896 | hp1 | a0003 | c0004 | t0001 | g0278 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02897 | hp2 | a0002 | c0007 | t0001 | g0007 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0306 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0269 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02970 | hp1 | a0005 | c0015 | t0001 | g0033 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0305 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02976 | hp1 | a0006 | c0038 | t0001 | g0281 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0303 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0025 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03041 | hp2 | a0017 | c0024 | t0001 | g0083 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0276 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03098 | hp2 | a0018 | c0029 | t0001 | g0261 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0291 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0297 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03139 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03195 | hp1 | a0019 | c0021 | t0001 | g0027 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03195 | hp2 | a0003 | c0036 | t0001 | g0274 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03209 | hp1 | a0003 | c0011 | t0001 | g0032 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03209 | hp2 | a0003 | c0004 | t0001 | g0300 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0292 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03453 | hp1 | a0003 | c0012 | t0001 | g0279 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0024 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03486 | hp1 | a0003 | c0004 | t0001 | g0290 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03486 | hp2 | a0001 | c0008 | t0001 | g0125 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0254 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0006 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03516 | hp1 | a0003 | c0009 | t0001 | g0039 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03516 | hp2 | a0020 | c0037 | t0001 | g0046 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03540 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03579 | hp1 | a0003 | c0011 | t0001 | g0045 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03579 | hp2 | a0021 | c0027 | t0001 | g0262 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0238 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0218 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03710 | hp2 | a0004 | c0005 | t0001 | g0263 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0251 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18522 | hp1 | a0003 | c0012 | t0001 | g0277 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18522 | hp2 | a0004 | c0005 | t0001 | g0264 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | CHB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0228 | EAS | CHB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0273 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0224 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18945 | hp2 | a0001 | c0006 | t0001 | g0019 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0214 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0222 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18952 | hp1 | a0001 | c0019 | t0001 | g0164 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18956 | hp2 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0225 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0213 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0215 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18975 | hp1 | a0010 | c0017 | t0001 | g0156 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18978 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18981 | hp1 | a0010 | c0017 | t0001 | g0157 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18981 | hp2 | a0022 | c0041 | t0001 | g0108 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0227 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19003 | hp2 | a0023 | c0033 | t0001 | g0242 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19010 | hp1 | a0001 | c0019 | t0001 | g0163 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19030 | hp1 | a0005 | c0010 | t0001 | g0037 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0126 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19043 | hp1 | a0002 | c0007 | t0001 | g0259 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19058 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19060 | hp1 | a0024 | c0022 | t0001 | g0030 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19062 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19063 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19064 | hp2 | a0001 | c0006 | t0001 | g0019 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19068 | hp1 | a0003 | c0004 | t0001 | g0284 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19077 | hp2 | a0008 | c0020 | t0001 | g0319 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA19240 | hp2 | a0003 | c0009 | t0001 | g0043 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA20129 | hp1 | a0001 | c0008 | t0001 | g0124 | AFR | ASW | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA20129 | hp2 | a0003 | c0004 | t0001 | g0272 | AFR | ASW | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA20805 | hp2 | a0002 | c0003 | t0001 | g0237 | EUR | TSI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02109 | hp1 | a0002 | c0014 | t0001 | g0012 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02109 | hp2 | a0006 | c0035 | t0001 | g0282 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02559 | hp1 | a0004 | c0005 | t0001 | g0081 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG02559 | hp2 | a0005 | c0010 | t0001 | g0038 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0302 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| HG03471 | hp2 | a0006 | c0016 | t0001 | g0051 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA20300 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | USA | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0304 | AFR | USA | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA21309 | hp1 | a0003 | c0034 | t0001 | g0050 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0203 | REF | REF | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0004 | REF | REF | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98199407 | C | T | 1 | a0011 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.2761G>A | p.Glu921Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 2869/3265 | 2761/2787 | 921/928 | chr9 | 98199407 | |||
| chr9:98199487 | C | T | 3 | a0006 a0009 a0019 |
7 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.2681G>A | p.Arg894Gln | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 2789/3265 | 2681/2787 | 894/928 | chr9 | 98199487 | |||
| chr9:98208732 | G | A | 1 | a0014 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2086C>T | p.Arg696Cys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2194/3265 | 2086/2787 | 696/928 | chr9 | 98208732 | |||
| chr9:98208815 | C | T | 1 | a0018 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2003G>A | p.Arg668His | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2111/3265 | 2003/2787 | 668/928 | chr9 | 98208815 | |||
| chr9:98208816 | G | A | 1 | a0020 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2002C>T | p.Arg668Cys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2110/3265 | 2002/2787 | 668/928 | chr9 | 98208816 | |||
| chr9:98208846 | G | A | 1 | a0012 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1972C>T | p.Arg658Trp | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2080/3265 | 1972/2787 | 658/928 | chr9 | 98208846 | |||
| chr9:98209032 | C | T | 1 | a0015 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1786G>A | p.Glu596Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 1894/3265 | 1786/2787 | 596/928 | chr9 | 98209032 | |||
| chr9:98209050 | G | T | 1 | a0022 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1768C>A | p.His590Asn | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 1876/3265 | 1768/2787 | 590/928 | chr9 | 98209050 | |||
| chr9:98210833 | A | C | 1 | a0007 | 2 | HG01071.hp2 HG02698.hp1 |
missense_variant | MODERATE | c.1496T>G | p.Leu499Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/13 | 1604/3265 | 1496/2787 | 499/928 | chr9 | 98210833 | |||
| chr9:98213130 | T | C | 1 | a0023 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1463A>G | p.Lys488Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/13 | 1571/3265 | 1463/2787 | 488/928 | chr9 | 98213130 | |||
| chr9:98213199 | C | T | 1 | a0010 | 2 | NA18975.hp1 NA18981.hp1 |
missense_variant | MODERATE | c.1394G>A | p.Arg465Gln | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/13 | 1502/3265 | 1394/2787 | 465/928 | chr9 | 98213199 | |||
| chr9:98220933 | A | G | 3 | a0016 a0019 a0021 |
3 | HG02818.hp2 HG03195.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1274T>C | p.Val425Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1382/3265 | 1274/2787 | 425/928 | chr9 | 98220933 | |||
| chr9:98221047 | G | A | 2 | a0005 a0013 |
7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
missense_variant | MODERATE | c.1160C>T | p.Ala387Val | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1268/3265 | 1160/2787 | 387/928 | chr9 | 98221047 | |||
| chr9:98229148 | C | A | 10 | a0002 a0009 a0012 others(7): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
missense_variant&splice_region_variant | MODERATE | c.782G>T | p.Gly261Val | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/13 | 890/3265 | 782/2787 | 261/928 | chr9 | 98229148 | |||
| chr9:98233439 | A | G | 16 | a0002 a0003 a0004 others(13): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
missense_variant | MODERATE | c.758T>C | p.Leu253Ser | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/13 | 866/3265 | 758/2787 | 253/928 | chr9 | 98233439 | |||
| chr9:98233476 | G | T | 11 | a0002 a0004 a0009 others(8): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
missense_variant | MODERATE | c.721C>A | p.Pro241Thr | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/13 | 829/3265 | 721/2787 | 241/928 | chr9 | 98233476 | |||
| chr9:98244129 | C | T | 1 | a0017 | 1 | HG03041.hp2 | missense_variant&splice_region_variant | MODERATE | c.512G>A | p.Gly171Glu | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/13 | 620/3265 | 512/2787 | 171/928 | chr9 | 98244129 | |||
| chr9:98255274 | A | C | 1 | a0013 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.268T>G | p.Leu90Val | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 376/3265 | 268/2787 | 90/928 | chr9 | 98255274 | |||
| chr9:98255283 | C | T | 1 | a0024 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.259G>A | p.Ala87Thr | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 367/3265 | 259/2787 | 87/928 | chr9 | 98255283 | |||
| chr9:98255541 | T | C | 1 | a0008 | 2 | HG02129.hp1 NA19077.hp2 |
start_lost | HIGH | c.1A>G | p.Met1? | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 109/3265 | 1/2787 | 1/928 | chr9 | 98255541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98199408 | G | A | 1 | a0002c0030 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.2760C>T | p.Ser920Ser | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 2868/3265 | 2760/2787 | 920/928 | chr9 | 98199408 | |||
| chr9:98200330 | C | T | 3 | a0003c0036 a0006c0035 a0006c0038 |
3 | HG02109.hp2 HG02976.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.2502G>A | p.Lys834Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/13 | 2610/3265 | 2502/2787 | 834/928 | chr9 | 98200330 | |||
| chr9:98201593 | G | A | 1 | a0001c0019 | 2 | NA18952.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.2343C>T | p.His781His | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/13 | 2451/3265 | 2343/2787 | 781/928 | chr9 | 98201593 | |||
| chr9:98208832 | G | A | 1 | a0001c0006 | 7 | HG01346.hp1 HG01993.hp1 HG02273.hp2 others(4): Show |
synonymous_variant | LOW | c.1986C>T | p.Arg662Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2094/3265 | 1986/2787 | 662/928 | chr9 | 98208832 | |||
| chr9:98209066 | T | C | 30 | a0001c0001 a0001c0039 a0002c0003 others(27): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
synonymous_variant | LOW | c.1752A>G | p.Ala584Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 1860/3265 | 1752/2787 | 584/928 | chr9 | 98209066 | |||
| chr9:98210754 | G | C | 2 | a0001c0008 a0003c0012 |
9 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.1575C>G | p.Ala525Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/13 | 1683/3265 | 1575/2787 | 525/928 | chr9 | 98210754 | |||
| chr9:98220947 | C | T | 2 | a0003c0036 a0006c0035 |
2 | HG02109.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1260G>A | p.Lys420Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1368/3265 | 1260/2787 | 420/928 | chr9 | 98220947 | |||
| chr9:98221118 | C | T | 1 | a0001c0039 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.1089G>A | p.Arg363Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1197/3265 | 1089/2787 | 363/928 | chr9 | 98221118 | |||
| chr9:98221201 | G | A | 1 | a0003c0026 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.1006C>T | p.Leu336Leu | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1114/3265 | 1006/2787 | 336/928 | chr9 | 98221201 | |||
| chr9:98233438 | C | T | 1 | a0003c0034 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.759G>A | p.Leu253Leu | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/13 | 867/3265 | 759/2787 | 253/928 | chr9 | 98233438 | |||
| chr9:98244056 | A | T | 6 | a0003c0009 a0003c0026 a0005c0010 others(3): Show |
14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
synonymous_variant | LOW | c.585T>A | p.Ala195Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/13 | 693/3265 | 585/2787 | 195/928 | chr9 | 98244056 | |||
| chr9:98251834 | G | T | 1 | a0005c0015 | 2 | HG01884.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.462C>A | p.Thr154Thr | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/13 | 570/3265 | 462/2787 | 154/928 | chr9 | 98251834 | |||
| chr9:98255395 | A | G | 3 | a0002c0014 a0009c0013 a0019c0021 |
5 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
synonymous_variant | LOW | c.147T>C | p.Cys49Cys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 255/3265 | 147/2787 | 49/928 | chr9 | 98255395 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98199371 | G | T | 1 | a0003c0004t0003 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 10 | chr9 | 98199371 | ||||||
| chr9:98255552 | C | T | 1 | a0001c0002t0002 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 11 | chr9 | 98255552 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98199646 | C | T | 29 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0002c0003t0001g0269 others(26): Show |
33 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2580-58G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199646 | |||||||
| chr9:98199670 | G | A | 14 | a0003c0004t0001g0025 a0003c0004t0001g0060 a0003c0004t0001g0270 others(11): Show |
15 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2580-82C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199670 | |||||||
| chr9:98199727 | A | G | 5 | a0002c0003t0001g0005 a0002c0003t0001g0212 a0002c0003t0001g0213 others(2): Show |
8 | NA18947.hp1 NA18968.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.2580-139T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199727 | |||||||
| chr9:98199845 | C | A | 11 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2580-257G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199845 | |||||||
| chr9:98199959 | A | G | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2579+294T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199959 | |||||||
| chr9:98200222 | G | C | 10 | a0001c0001t0001g0015 a0002c0003t0001g0208 a0002c0003t0001g0237 others(7): Show |
11 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.2579+31C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98200222 | |||||||
| chr9:98200380 | G | A | 1 | a0001c0002t0001g0091 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.2458-6C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200380 | |||||||
| chr9:98200462 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2458-88T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200462 | |||||||
| chr9:98200485 | G | A | 7 | a0003c0004t0001g0025 a0003c0004t0001g0270 a0003c0004t0001g0275 others(4): Show |
8 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2458-111C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200485 | |||||||
| chr9:98200520 | A | G | 197 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(194): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2458-146T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200520 | |||||||
| chr9:98200564 | T | TG | 12 | a0001c0001t0001g0056 a0001c0001t0001g0111 a0001c0001t0001g0117 others(9): Show |
12 | HG00642.hp1 HG01192.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.2458-191dupC | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200564 | |||||||
| chr9:98200572 | C | T | 52 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(49): Show |
61 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.2458-198G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200572 | |||||||
| chr9:98200721 | A | G | 54 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(51): Show |
63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2458-347T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200721 | |||||||
| chr9:98200742 | A | G | 159 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(156): Show |
180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2458-368T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200742 | |||||||
| chr9:98200744 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2458-370T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200744 | |||||||
| chr9:98200807 | G | T | 12 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(9): Show |
12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2458-433C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200807 | |||||||
| chr9:98201015 | C | CA | 9 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0089 others(6): Show |
10 | HG00438.hp2 HG00639.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2457+463dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201015 | |||||||
| chr9:98201015 | C | CAA | 12 | a0002c0003t0001g0310 a0003c0004t0001g0025 a0003c0004t0001g0060 others(9): Show |
13 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2457+462_2457+463d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201015 | |||||||
| chr9:98201015 | CA | C | 14 | a0001c0001t0001g0099 a0001c0001t0001g0190 a0001c0001t0001g0201 others(11): Show |
14 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2457+463delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201015 | |||||||
| chr9:98201180 | C | T | 54 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(51): Show |
63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2457+299G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201180 | |||||||
| chr9:98201371 | T | C | 159 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(156): Show |
180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2457+108A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201371 | |||||||
| chr9:98201677 | G | A | 8 | a0003c0036t0001g0274 a0006c0016t0001g0051 a0006c0016t0001g0052 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2272-13C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201677 | |||||||
| chr9:98201695 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0117 a0001c0001t0001g0308 others(1): Show |
4 | HG00642.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2272-31G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201695 | |||||||
| chr9:98201841 | A | G | 1 | a0019c0021t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2272-177T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201841 | |||||||
| chr9:98201858 | C | T | 1 | a0018c0029t0001g0261 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2272-194G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201858 | |||||||
| chr9:98201932 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0186 a0001c0001t0001g0189 others(8): Show |
12 | HG01099.hp2 HG01192.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.2272-268G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201932 | |||||||
| chr9:98202039 | T | C | 11 | a0003c0004t0001g0025 a0003c0004t0001g0060 a0003c0004t0001g0270 others(8): Show |
12 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2272-375A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202039 | |||||||
| chr9:98202082 | A | C | 161 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(158): Show |
182 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.2272-418T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202082 | |||||||
| chr9:98202170 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2272-506C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202170 | |||||||
| chr9:98202186 | C | T | 1 | a0001c0006t0001g0154 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2272-522G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202186 | |||||||
| chr9:98202188 | C | A | 62 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
70 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2272-524G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202188 | |||||||
| chr9:98202369 | C | T | 197 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(194): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2272-705G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202369 | |||||||
| chr9:98202419 | T | C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(194): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2272-755A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202419 | |||||||
| chr9:98202440 | G | A | 1 | a0001c0002t0001g0168 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2272-776C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202440 | |||||||
| chr9:98202467 | C | T | 164 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(161): Show |
185 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.2272-803G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202467 | |||||||
| chr9:98202631 | G | A | 1 | a0018c0029t0001g0261 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2271+657C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202631 | |||||||
| chr9:98202662 | C | T | 158 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(155): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2271+626G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202662 | |||||||
| chr9:98202702 | G | T | 2 | a0001c0002t0001g0177 a0001c0002t0001g0179 |
2 | HG00741.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2271+586C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202702 | |||||||
| chr9:98202726 | C | T | 226 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(223): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.2271+562G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202726 | |||||||
| chr9:98202727 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2271+561C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202727 | |||||||
| chr9:98202809 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2271+479C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202809 | |||||||
| chr9:98203025 | C | A | 226 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(223): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.2271+263G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203025 | |||||||
| chr9:98203068 | C | T | 1 | a0014c0031t0001g0246 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2271+220G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203068 | |||||||
| chr9:98203069 | G | A | 1 | a0002c0003t0001g0220 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2271+219C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203069 | |||||||
| chr9:98203114 | G | C | 1 | a0018c0029t0001g0261 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2271+174C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203114 | |||||||
| chr9:98203141 | T | G | 12 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(9): Show |
12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2271+147A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203141 | |||||||
| chr9:98203145 | T | C | 2 | a0003c0004t0001g0299 a0003c0004t0001g0300 |
2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2271+143A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203145 | |||||||
| chr9:98203169 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2271+119C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203169 | |||||||
| chr9:98203190 | C | T | 237 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(234): Show |
260 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2271+98G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203190 | |||||||
| chr9:98203275 | T | C | 1 | a0016c0025t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2271+13A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203275 | |||||||
| chr9:98203934 | G | A | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2151-526C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98203934 | |||||||
| chr9:98204008 | T | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
70 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2151-600A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204008 | |||||||
| chr9:98204170 | TC | T | 5 | a0006c0016t0001g0051 a0006c0016t0001g0052 a0009c0013t0001g0028 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-763delG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204170 | |||||||
| chr9:98204251 | G | T | 1 | a0005c0015t0001g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2151-843C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204251 | |||||||
| chr9:98204319 | G | A | 1 | a0005c0010t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2151-911C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204319 | |||||||
| chr9:98204358 | C | T | 1 | a0003c0004t0001g0299 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2151-950G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204358 | |||||||
| chr9:98204388 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2151-980G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204388 | |||||||
| chr9:98204426 | C | A | 3 | a0003c0004t0001g0011 a0003c0004t0001g0272 a0003c0004t0001g0273 |
5 | HG02717.hp1 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-1018G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204426 | |||||||
| chr9:98204509 | C | A | 4 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(1): Show |
4 | HG00323.hp2 HG03942.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151-1101G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204509 | |||||||
| chr9:98204558 | G | T | 29 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(26): Show |
29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2151-1150C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204558 | |||||||
| chr9:98204559 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2151-1151C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204559 | |||||||
| chr9:98204632 | C | CA | 7 | a0005c0010t0001g0037 a0005c0010t0001g0038 a0005c0010t0001g0040 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2151-1225dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204632 | |||||||
| chr9:98204637 | G | A | 11 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2151-1229C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204637 | |||||||
| chr9:98204801 | T | TG | 33 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0090 others(30): Show |
38 | HG00597.hp1 HG01106.hp1 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.2151-1394dupC | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204801 | |||||||
| chr9:98204883 | A | G | 32 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0003c0004t0001g0011 others(29): Show |
35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.2151-1475T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204883 | |||||||
| chr9:98205279 | A | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2151-1871T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205279 | |||||||
| chr9:98205304 | C | G | 1 | a0002c0003t0001g0234 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2151-1896G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205304 | |||||||
| chr9:98205515 | T | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2151-2107A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205515 | |||||||
| chr9:98205576 | T | C | 10 | a0001c0001t0001g0015 a0002c0003t0001g0208 a0002c0003t0001g0237 others(7): Show |
11 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.2151-2168A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205576 | |||||||
| chr9:98205578 | A | C | 1 | a0001c0002t0001g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2151-2170T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205578 | |||||||
| chr9:98205601 | C | CA | 28 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(25): Show |
28 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2151-2194dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205601 | |||||||
| chr9:98205603 | G | A | 28 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(25): Show |
28 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2151-2195C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205603 | |||||||
| chr9:98205643 | C | A | 1 | a0019c0021t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2151-2235G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205643 | |||||||
| chr9:98205669 | C | G | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2151-2261G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205669 | |||||||
| chr9:98205722 | T | C | 4 | a0002c0003t0001g0269 a0002c0003t0001g0310 a0002c0014t0001g0012 others(1): Show |
5 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2151-2314A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205722 | |||||||
| chr9:98205853 | C | T | 16 | a0002c0003t0001g0023 a0002c0003t0001g0211 a0002c0003t0001g0217 others(13): Show |
17 | HG01106.hp1 HG01928.hp1 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.2151-2445G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205853 | |||||||
| chr9:98205944 | A | G | 1 | a0001c0002t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2151-2536T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205944 | |||||||
| chr9:98206007 | C | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
76 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2151-2599G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206007 | |||||||
| chr9:98206208 | A | G | 99 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(96): Show |
112 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2150+2460T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206208 | |||||||
| chr9:98206316 | T | C | 199 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(196): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2150+2352A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206316 | |||||||
| chr9:98206321 | A | G | 5 | a0001c0006t0001g0018 a0001c0006t0001g0019 a0001c0006t0001g0139 others(2): Show |
7 | HG01346.hp1 HG01993.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150+2347T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206321 | |||||||
| chr9:98206538 | T | C | 56 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(53): Show |
65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2150+2130A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206538 | |||||||
| chr9:98206558 | C | T | 1 | a0002c0003t0001g0215 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2150+2110G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206558 | |||||||
| chr9:98206600 | C | T | 29 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(26): Show |
29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2150+2068G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206600 | |||||||
| chr9:98207066 | G | A | 158 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0057 others(155): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2150+1602C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207066 | |||||||
| chr9:98207201 | T | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2150+1467A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207201 | |||||||
| chr9:98207431 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2150+1237C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207431 | |||||||
| chr9:98207436 | G | A | 2 | a0001c0002t0001g0180 a0001c0002t0001g0181 |
2 | NA18951.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2150+1232C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207436 | |||||||
| chr9:98207468 | T | C | 2 | a0004c0005t0001g0082 a0004c0005t0001g0268 |
2 | HG00140.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2150+1200A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207468 | |||||||
| chr9:98207507 | T | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0090 others(30): Show |
38 | HG00597.hp1 HG01106.hp1 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.2150+1161A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207507 | |||||||
| chr9:98207572 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2150+1096A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207572 | |||||||
| chr9:98207743 | C | T | 2 | a0003c0026t0001g0044 a0003c0034t0001g0050 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2150+925G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207743 | |||||||
| chr9:98207775 | C | T | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2150+893G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207775 | |||||||
| chr9:98207811 | C | T | 2 | a0003c0004t0001g0273 a0018c0029t0001g0261 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2150+857G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207811 | |||||||
| chr9:98207812 | G | A | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2150+856C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207812 | |||||||
| chr9:98207854 | C | A | 29 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(26): Show |
29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2150+814G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207854 | |||||||
| chr9:98207857 | C | T | 1 | a0002c0014t0001g0012 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2150+811G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207857 | |||||||
| chr9:98208007 | A | G | 56 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(53): Show |
65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2150+661T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208007 | |||||||
| chr9:98208025 | G | A | 11 | a0003c0004t0001g0025 a0003c0004t0001g0060 a0003c0004t0001g0270 others(8): Show |
12 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150+643C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208025 | |||||||
| chr9:98208144 | A | G | 12 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(9): Show |
12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150+524T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208144 | |||||||
| chr9:98208278 | C | T | 30 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(27): Show |
30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2150+390G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208278 | |||||||
| chr9:98208324 | G | A | 30 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(27): Show |
30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2150+344C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208324 | |||||||
| chr9:98208403 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0118 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150+265C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208403 | |||||||
| chr9:98208443 | G | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
76 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2150+225C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208443 | |||||||
| chr9:98208455 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2150+213G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208455 | |||||||
| chr9:98208568 | C | CA | 11 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150+99_2150+100in others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208568 | |||||||
| chr9:98208568 | C | CG | 216 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(213): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2150+99_2150+100in others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208568 | |||||||
| chr9:98208570 | T | A | 1 | a0022c0041t0001g0108 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2150+98A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208570 | |||||||
| chr9:98208574 | A | T | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2150+94T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208574 | |||||||
| chr9:98208599 | A | G | 228 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2150+69T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208599 | |||||||
| chr9:98208643 | C | G | 1 | a0001c0002t0001g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2150+25G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208643 | |||||||
| chr9:98209234 | C | A | 1 | a0022c0041t0001g0108 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1674-90G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209234 | |||||||
| chr9:98209254 | G | A | 5 | a0006c0016t0001g0051 a0006c0016t0001g0052 a0009c0013t0001g0028 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-110C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209254 | |||||||
| chr9:98209387 | G | C | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1674-243C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209387 | |||||||
| chr9:98209454 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1674-310C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209454 | |||||||
| chr9:98209538 | G | A | 1 | a0003c0004t0001g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1674-394C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209538 | |||||||
| chr9:98209618 | T | A | 1 | a0022c0041t0001g0108 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1674-474A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209618 | |||||||
| chr9:98209624 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0118 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1674-480T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209624 | |||||||
| chr9:98209703 | C | A | 5 | a0006c0016t0001g0051 a0006c0016t0001g0052 a0009c0013t0001g0028 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-559G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209703 | |||||||
| chr9:98209710 | CT | C | 14 | a0002c0003t0001g0310 a0003c0004t0001g0048 a0003c0004t0001g0101 others(11): Show |
14 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1674-567delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209710 | |||||||
| chr9:98209718 | TTTCC | T | 7 | a0001c0001t0001g0206 a0003c0004t0001g0060 a0003c0004t0001g0272 others(4): Show |
7 | HG02615.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-578_1674-575d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209718 | |||||||
| chr9:98209730 | C | CTTCTTTC others(2): Show |
79 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(76): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1674-587_1674-586i others(11): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209730 | |||||||
| chr9:98209730 | C | T | 1 | a0004c0005t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1674-586G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209730 | |||||||
| chr9:98209734 | C | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0056 others(25): Show |
33 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-590G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209734 | |||||||
| chr9:98209738 | T | C | 108 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(105): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1674-594A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209738 | |||||||
| chr9:98209741 | C | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0056 others(25): Show |
33 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-597G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209741 | |||||||
| chr9:98209743 | T | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0056 others(25): Show |
33 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-599A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209743 | |||||||
| chr9:98209751 | C | CT | 23 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0063 others(20): Show |
26 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1674-608dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209751 | |||||||
| chr9:98209754 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0001g0104 others(2): Show |
7 | HG02132.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674-610G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209754 | |||||||
| chr9:98209755 | CT | C | 25 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0064 others(22): Show |
27 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1674-612delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209755 | |||||||
| chr9:98209756 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0001g0104 others(2): Show |
7 | HG02132.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674-612A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTCC | 50 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(47): Show |
56 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTCCCTTC others(25): Show |
1 | a0002c0003t0001g0250 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1674-613_1674-612i others(34): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTCCTTCC | 18 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0070 others(15): Show |
18 | HG00438.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(9): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTCCTTCC others(4): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0116 a0003c0004t0001g0025 others(2): Show |
6 | HG00140.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTCCTTCC others(8): Show |
5 | a0001c0001t0001g0205 a0002c0003t0001g0221 a0002c0003t0001g0237 others(2): Show |
5 | HG00733.hp1 HG02015.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(17): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTCCTTCC others(12): Show |
2 | a0003c0004t0001g0305 a0003c0004t0001g0306 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1674-613_1674-612i others(21): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCC | 13 | a0001c0001t0001g0146 a0001c0008t0001g0124 a0002c0003t0001g0006 others(10): Show |
16 | HG00323.hp2 HG00597.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1674-616_1674-613d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCCTTC others(1): Show |
8 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0002c0003t0001g0310 others(5): Show |
8 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1674-620_1674-613d others(10): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCCTTC others(5): Show |
4 | a0001c0001t0001g0160 a0003c0004t0001g0101 a0003c0034t0001g0050 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674-624_1674-613d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCCTTC others(9): Show |
2 | a0016c0025t0001g0042 a0018c0029t0001g0261 |
2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1674-628_1674-613d others(18): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCCTTC others(13): Show |
4 | a0002c0003t0001g0006 a0003c0004t0001g0048 a0003c0009t0001g0043 others(1): Show |
4 | HG01081.hp1 HG01516.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674-632_1674-613d others(22): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCCTTC others(17): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0003c0004t0003g0049 |
3 | HG01891.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1674-636_1674-613d others(26): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | T | TTTCCTTC others(29): Show |
1 | a0001c0002t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1674-648_1674-613d others(38): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | TTTCC | T | 83 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0001c0001t0001g0136 others(80): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1674-616_1674-613d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | TTTCCTTC others(1): Show |
T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0145 a0008c0020t0001g0318 |
3 | HG01069.hp2 HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1674-620_1674-613d others(10): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209756 | TTTCCTTC others(5): Show |
T | 2 | a0009c0013t0001g0028 a0009c0013t0001g0029 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1674-624_1674-613d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | |||||||
| chr9:98209758 | T | C | 30 | a0001c0001t0001g0057 a0001c0001t0001g0076 a0001c0001t0001g0080 others(27): Show |
30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1674-614A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209758 | |||||||
| chr9:98209793 | T | TCCTTCCT others(7): Show |
1 | a0022c0041t0001g0108 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1674-650_1674-649i others(16): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209793 | |||||||
| chr9:98209795 | T | C | 2 | a0001c0001t0001g0072 a0018c0029t0001g0261 |
2 | HG03098.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1674-651A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209795 | |||||||
| chr9:98209880 | C | G | 230 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1674-736G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209880 | |||||||
| chr9:98209929 | A | G | 1 | a0001c0002t0001g0307 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1673+727T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209929 | |||||||
| chr9:98209940 | CACCT | C | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1673+712_1673+715d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209940 | |||||||
| chr9:98209950 | TTCCGA | T | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1673+701_1673+705d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209950 | |||||||
| chr9:98209963 | G | T | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1673+693C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209963 | |||||||
| chr9:98209973 | C | T | 12 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(9): Show |
12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1673+683G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209973 | |||||||
| chr9:98209990 | C | CT | 6 | a0001c0002t0001g0183 a0002c0003t0001g0269 a0002c0003t0001g0310 others(3): Show |
7 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1673+665dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209990 | |||||||
| chr9:98209990 | CT | C | 37 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(34): Show |
37 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1673+665delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209990 | |||||||
| chr9:98209990 | CTTT | C | 11 | a0001c0001t0001g0015 a0002c0003t0001g0208 a0002c0003t0001g0237 others(8): Show |
12 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1673+663_1673+665d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209990 | |||||||
| chr9:98209993 | T | C | 116 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(113): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1673+663A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209993 | |||||||
| chr9:98209994 | T | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0118 others(2): Show |
5 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673+662A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209994 | |||||||
| chr9:98210022 | C | T | 1 | a0003c0004t0003g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1673+634G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210022 | |||||||
| chr9:98210106 | A | G | 225 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(222): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1673+550T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210106 | |||||||
| chr9:98210268 | C | T | 1 | a0003c0004t0001g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1673+388G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210268 | |||||||
| chr9:98210269 | A | C | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1673+387T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210269 | |||||||
| chr9:98210299 | T | C | 1 | a0013c0023t0001g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1673+357A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210299 | |||||||
| chr9:98210318 | G | A | 3 | a0002c0003t0001g0213 a0002c0003t0001g0214 a0002c0003t0001g0252 |
3 | NA18947.hp1 NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1673+338C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210318 | |||||||
| chr9:98210326 | T | C | 11 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1673+330A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210326 | |||||||
| chr9:98210367 | T | G | 1 | a0003c0012t0001g0271 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1673+289A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210367 | |||||||
| chr9:98210403 | G | T | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1673+253C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210403 | |||||||
| chr9:98210417 | T | C | 229 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(226): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1673+239A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210417 | |||||||
| chr9:98210451 | G | A | 2 | a0006c0016t0001g0051 a0006c0016t0001g0052 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1673+205C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210451 | |||||||
| chr9:98210463 | T | A | 1 | a0002c0003t0001g0217 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1673+193A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210463 | |||||||
| chr9:98210471 | T | C | 1 | a0007c0018t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1673+185A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210471 | |||||||
| chr9:98210628 | C | T | 1 | a0002c0003t0001g0237 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1673+28G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210628 | |||||||
| chr9:98210896 | A | AGAGGCCT | 220 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(217): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1486-60_1486-54dup others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98210896 | |||||||
| chr9:98211048 | G | A | 17 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(14): Show |
17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1486-205C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211048 | |||||||
| chr9:98211140 | C | T | 1 | a0003c0004t0001g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1486-297G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211140 | |||||||
| chr9:98211253 | C | T | 2 | a0007c0018t0001g0078 a0007c0018t0001g0079 |
2 | HG01071.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1486-410G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211253 | |||||||
| chr9:98211376 | C | T | 30 | a0001c0001t0001g0015 a0001c0001t0001g0160 a0001c0001t0001g0167 others(27): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1486-533G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211376 | |||||||
| chr9:98211505 | T | A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1486-662A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211505 | |||||||
| chr9:98211512 | C | A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1486-669G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211512 | |||||||
| chr9:98211550 | T | C | 56 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(53): Show |
65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1486-707A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211550 | |||||||
| chr9:98211570 | T | A | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-727A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211570 | |||||||
| chr9:98211618 | T | C | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-775A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211618 | |||||||
| chr9:98211619 | G | T | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-776C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211619 | |||||||
| chr9:98211800 | C | CT | 92 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(89): Show |
103 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1486-958dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211800 | |||||||
| chr9:98211861 | G | A | 1 | a0001c0002t0001g0119 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1486-1018C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211861 | |||||||
| chr9:98211909 | T | A | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-1066A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211909 | |||||||
| chr9:98211954 | C | T | 4 | a0003c0011t0001g0032 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG02615.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486-1111G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211954 | |||||||
| chr9:98212061 | C | T | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1485+1047G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212061 | |||||||
| chr9:98212062 | G | A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1485+1046C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212062 | |||||||
| chr9:98212088 | C | T | 1 | a0001c0019t0001g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1485+1020G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212088 | |||||||
| chr9:98212163 | C | A | 11 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1485+945G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212163 | |||||||
| chr9:98212253 | G | T | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1485+855C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212253 | |||||||
| chr9:98212260 | T | G | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1485+848A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212260 | |||||||
| chr9:98212394 | T | C | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1485+714A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212394 | |||||||
| chr9:98212474 | G | A | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1485+634C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212474 | |||||||
| chr9:98212480 | C | T | 4 | a0001c0001t0001g0175 a0002c0003t0001g0215 a0002c0003t0001g0240 others(1): Show |
4 | HG00639.hp1 HG01496.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+628G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212480 | |||||||
| chr9:98212506 | C | CT | 142 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(139): Show |
162 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1485+601dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212506 | |||||||
| chr9:98212506 | CT | C | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1485+601delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212506 | |||||||
| chr9:98212705 | C | T | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1485+403G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212705 | |||||||
| chr9:98212788 | G | A | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1485+320C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212788 | |||||||
| chr9:98212801 | G | C | 1 | a0016c0025t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1485+307C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212801 | |||||||
| chr9:98213036 | C | T | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1485+72G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98213036 | |||||||
| chr9:98213072 | G | T | 1 | a0018c0029t0001g0261 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1485+36C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98213072 | |||||||
| chr9:98213076 | G | A | 5 | a0003c0004t0001g0288 a0003c0004t0001g0289 a0003c0004t0001g0293 others(2): Show |
5 | HG00323.hp1 HG00642.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+32C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98213076 | |||||||
| chr9:98213266 | C | T | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1375-48G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213266 | |||||||
| chr9:98213311 | T | G | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1375-93A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213311 | |||||||
| chr9:98213412 | G | A | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-194C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213412 | |||||||
| chr9:98213555 | A | G | 74 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(71): Show |
76 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1375-337T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213555 | |||||||
| chr9:98213582 | C | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(40): Show |
45 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1375-364G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213582 | |||||||
| chr9:98213804 | A | G | 229 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(226): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1375-586T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213804 | |||||||
| chr9:98213849 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0116 |
2 | NA18941.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1375-631A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213849 | |||||||
| chr9:98213958 | A | G | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1375-740T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213958 | |||||||
| chr9:98214059 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(1): Show |
4 | HG00323.hp2 HG03942.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-841G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214059 | |||||||
| chr9:98214160 | A | C | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1375-942T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214160 | |||||||
| chr9:98214190 | ATGGCCAG others(133): Show |
A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1375-1112_1375-973 others(3): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214190 | |||||||
| chr9:98214198 | GTTGATTT others(63): Show |
G | 54 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(51): Show |
63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1375-1050_1375-981 others(73): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214198 | |||||||
| chr9:98214234 | G | A | 1 | a0001c0002t0001g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1375-1016C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214234 | |||||||
| chr9:98214256 | C | T | 9 | a0001c0008t0001g0121 a0001c0008t0001g0122 a0001c0008t0001g0123 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1375-1038G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214256 | |||||||
| chr9:98214257 | G | A | 1 | a0001c0002t0001g0004 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1375-1039C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214257 | |||||||
| chr9:98214268 | A | G | 26 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0003c0004t0001g0024 others(23): Show |
27 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.1375-1050T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214268 | |||||||
| chr9:98214268 | ATTGATTT others(63): Show |
A | 72 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(69): Show |
74 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1375-1120_1375-105 others(74): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214268 | |||||||
| chr9:98214268 | ATTGATTT others(133): Show |
A | 2 | a0009c0013t0001g0028 a0009c0013t0001g0029 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1375-1190_1375-105 others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214268 | |||||||
| chr9:98214277 | GAAATGAA others(134): Show |
G | 1 | a0023c0033t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1375-1200_1375-106 others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214277 | |||||||
| chr9:98214396 | C | T | 29 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(26): Show |
29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1375-1178G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214396 | |||||||
| chr9:98214530 | T | A | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1375-1312A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214530 | |||||||
| chr9:98214536 | C | G | 41 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(38): Show |
43 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1375-1318G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214536 | |||||||
| chr9:98214537 | G | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(5): Show |
9 | HG00323.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1375-1319C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214537 | |||||||
| chr9:98214548 | GTTGATTT others(63): Show |
G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0204 |
2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1375-1400_1375-133 others(74): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214548 | |||||||
| chr9:98214583 | C | T | 1 | a0003c0004t0001g0302 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1375-1365G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214583 | |||||||
| chr9:98214592 | A | G | 75 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(72): Show |
77 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1375-1374T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214592 | |||||||
| chr9:98214607 | G | A | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-1389C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214607 | |||||||
| chr9:98214610 | G | A | 3 | a0001c0001t0001g0076 a0002c0003t0001g0209 a0002c0003t0001g0210 |
3 | HG01099.hp1 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1375-1392C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214610 | |||||||
| chr9:98214665 | C | T | 17 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(14): Show |
17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-1447G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214665 | |||||||
| chr9:98214838 | G | T | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-1620C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214838 | |||||||
| chr9:98214857 | T | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0305 a0003c0004t0001g0306 |
4 | HG02809.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-1639A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214857 | |||||||
| chr9:98214857 | T | C | 81 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(78): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1375-1639A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214857 | |||||||
| chr9:98215072 | A | C | 1 | a0001c0002t0001g0178 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1375-1854T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215072 | |||||||
| chr9:98215110 | C | T | 229 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(226): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1375-1892G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215110 | |||||||
| chr9:98215175 | T | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1375-1957A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215175 | |||||||
| chr9:98215225 | G | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0118 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-2007C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215225 | |||||||
| chr9:98215355 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0204 |
2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1375-2137C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215355 | |||||||
| chr9:98215484 | T | A | 2 | a0002c0003t0001g0022 a0004c0005t0001g0081 |
3 | HG01346.hp2 HG02300.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1375-2266A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215484 | |||||||
| chr9:98215492 | A | G | 1 | a0002c0003t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1375-2274T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215492 | |||||||
| chr9:98215592 | C | T | 11 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-2374G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215592 | |||||||
| chr9:98215757 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1375-2539G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215757 | |||||||
| chr9:98215801 | T | C | 49 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(46): Show |
49 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1375-2583A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215801 | |||||||
| chr9:98215949 | C | A | 1 | a0006c0016t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1375-2731G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215949 | |||||||
| chr9:98216012 | A | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1375-2794T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216012 | |||||||
| chr9:98216094 | C | T | 17 | a0003c0004t0001g0048 a0003c0004t0001g0101 a0003c0009t0001g0043 others(14): Show |
17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-2876G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216094 | |||||||
| chr9:98216172 | G | T | 8 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(5): Show |
9 | HG00323.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1375-2954C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216172 | |||||||
| chr9:98216260 | G | A | 90 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(87): Show |
101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1375-3042C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216260 | |||||||
| chr9:98216261 | T | A | 1 | a0002c0003t0001g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1375-3043A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216261 | |||||||
| chr9:98216344 | G | C | 83 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(80): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1375-3126C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216344 | |||||||
| chr9:98216380 | C | T | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-3162G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216380 | |||||||
| chr9:98216381 | G | T | 43 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(40): Show |
45 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1375-3163C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216381 | |||||||
| chr9:98216440 | G | A | 1 | a0001c0008t0001g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1375-3222C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216440 | |||||||
| chr9:98216450 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1375-3232A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216450 | |||||||
| chr9:98216608 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1375-3390G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216608 | |||||||
| chr9:98216620 | C | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1375-3402G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216620 | |||||||
| chr9:98216901 | T | A | 2 | a0002c0003t0001g0220 a0002c0003t0001g0228 |
2 | NA18612.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1375-3683A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216901 | |||||||
| chr9:98216988 | G | A | 73 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(70): Show |
75 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1375-3770C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216988 | |||||||
| chr9:98217061 | T | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1374+3772A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217061 | |||||||
| chr9:98217063 | T | C | 230 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1374+3770A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217063 | |||||||
| chr9:98217203 | G | A | 90 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(87): Show |
101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1374+3630C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217203 | |||||||
| chr9:98217211 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1374+3622T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217211 | |||||||
| chr9:98217232 | G | A | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1374+3601C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217232 | |||||||
| chr9:98217309 | G | A | 2 | a0002c0003t0001g0243 a0002c0003t0001g0244 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1374+3524C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217309 | |||||||
| chr9:98217314 | T | C | 1 | a0002c0014t0001g0012 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1374+3519A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217314 | |||||||
| chr9:98217392 | G | A | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+3441C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217392 | |||||||
| chr9:98217447 | C | G | 1 | a0001c0001t0001g0202 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1374+3386G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217447 | |||||||
| chr9:98217480 | G | A | 31 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(28): Show |
31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1374+3353C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217480 | |||||||
| chr9:98217520 | G | C | 2 | a0002c0003t0001g0243 a0002c0003t0001g0244 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1374+3313C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217520 | |||||||
| chr9:98217774 | G | A | 57 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(54): Show |
66 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1374+3059C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217774 | |||||||
| chr9:98217810 | G | A | 1 | a0001c0008t0001g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1374+3023C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217810 | |||||||
| chr9:98218024 | A | C | 2 | a0002c0003t0001g0243 a0002c0003t0001g0244 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1374+2809T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218024 | |||||||
| chr9:98218024 | A | T | 134 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0057 others(131): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1374+2809T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218024 | |||||||
| chr9:98218033 | T | C | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+2800A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218033 | |||||||
| chr9:98218246 | G | A | 2 | a0005c0015t0001g0033 a0005c0015t0001g0034 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1374+2587C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218246 | |||||||
| chr9:98218410 | C | CA | 140 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0057 others(137): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1374+2422dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218410 | |||||||
| chr9:98218484 | G | A | 5 | a0006c0016t0001g0051 a0006c0016t0001g0052 a0009c0013t0001g0028 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+2349C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218484 | |||||||
| chr9:98218521 | C | A | 56 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(53): Show |
65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1374+2312G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218521 | |||||||
| chr9:98218562 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1374+2271C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218562 | |||||||
| chr9:98218583 | A | C | 56 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(53): Show |
65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1374+2250T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218583 | |||||||
| chr9:98218630 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1374+2203G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218630 | |||||||
| chr9:98218650 | A | G | 1 | a0002c0003t0001g0250 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1374+2183T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218650 | |||||||
| chr9:98218691 | T | C | 149 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0057 others(146): Show |
161 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1374+2142A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218691 | |||||||
| chr9:98218746 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1374+2087T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218746 | |||||||
| chr9:98218823 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0072 others(2): Show |
5 | NA18941.hp2 NA18951.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1374+2010G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218823 | |||||||
| chr9:98218824 | G | A | 1 | a0008c0020t0001g0319 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1374+2009C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218824 | |||||||
| chr9:98218860 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1374+1973G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218860 | |||||||
| chr9:98218877 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0118 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+1956G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218877 | |||||||
| chr9:98219099 | C | T | 2 | a0003c0004t0001g0293 a0003c0004t0001g0301 |
2 | HG00642.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1374+1734G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219099 | |||||||
| chr9:98219100 | G | C | 1 | a0001c0002t0001g0134 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1374+1733C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219100 | |||||||
| chr9:98219127 | T | C | 1 | a0003c0004t0001g0296 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1374+1706A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219127 | |||||||
| chr9:98219161 | C | T | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+1672G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219161 | |||||||
| chr9:98219475 | T | G | 140 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0057 others(137): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1374+1358A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219475 | |||||||
| chr9:98219575 | G | A | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+1258C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219575 | |||||||
| chr9:98219587 | A | T | 2 | a0003c0004t0001g0296 a0003c0004t0001g0297 |
2 | HG01952.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1374+1246T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219587 | |||||||
| chr9:98219621 | G | A | 4 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(1): Show |
4 | HG00323.hp2 HG03942.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+1212C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219621 | |||||||
| chr9:98219624 | C | T | 9 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1374+1209G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219624 | |||||||
| chr9:98219833 | G | A | 1 | a0004c0005t0001g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1374+1000C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219833 | |||||||
| chr9:98220165 | G | A | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1374+668C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220165 | |||||||
| chr9:98220187 | C | A | 1 | a0001c0002t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1374+646G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220187 | |||||||
| chr9:98220277 | G | A | 2 | a0002c0003t0001g0269 a0002c0003t0001g0310 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1374+556C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220277 | |||||||
| chr9:98220321 | A | G | 1 | a0016c0025t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1374+512T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220321 | |||||||
| chr9:98220549 | T | G | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1374+284A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220549 | |||||||
| chr9:98220576 | T | C | 122 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1374+257A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220576 | |||||||
| chr9:98220676 | A | G | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+157T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220676 | |||||||
| chr9:98220743 | A | G | 2 | a0001c0019t0001g0163 a0001c0019t0001g0164 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1374+90T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220743 | |||||||
| chr9:98220766 | C | T | 2 | a0006c0016t0001g0051 a0006c0016t0001g0052 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1374+67G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220766 | |||||||
| chr9:98220798 | G | A | 5 | a0003c0004t0001g0288 a0003c0004t0001g0289 a0003c0004t0001g0293 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+35C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220798 | |||||||
| chr9:98221284 | C | G | 223 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(220): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.979-56G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221284 | |||||||
| chr9:98221322 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.979-94C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221322 | |||||||
| chr9:98221544 | C | G | 83 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(80): Show |
96 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.979-316G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221544 | |||||||
| chr9:98221603 | C | T | 1 | a0021c0027t0001g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979-375G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221603 | |||||||
| chr9:98221787 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0204 |
2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.979-559C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221787 | |||||||
| chr9:98221909 | T | G | 57 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(54): Show |
69 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.979-681A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221909 | |||||||
| chr9:98221929 | C | G | 1 | a0004c0005t0001g0266 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.979-701G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221929 | |||||||
| chr9:98221943 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.979-715C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221943 | |||||||
| chr9:98222137 | T | C | 1 | a0021c0027t0001g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979-909A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222137 | |||||||
| chr9:98222549 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.979-1321C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222549 | |||||||
| chr9:98222573 | C | T | 58 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(55): Show |
70 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.979-1345G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222573 | |||||||
| chr9:98222622 | G | A | 1 | a0002c0003t0001g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.979-1394C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222622 | |||||||
| chr9:98222664 | T | C | 162 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.979-1436A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222664 | |||||||
| chr9:98222703 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.979-1475G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222703 | |||||||
| chr9:98222708 | C | T | 1 | a0006c0016t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.979-1480G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222708 | |||||||
| chr9:98223029 | C | T | 54 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0076 others(51): Show |
63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.979-1801G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223029 | |||||||
| chr9:98223030 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(101): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.979-1802C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223030 | |||||||
| chr9:98223085 | T | A | 28 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0085 others(25): Show |
28 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-1857A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223085 | |||||||
| chr9:98223105 | C | T | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1877G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223105 | |||||||
| chr9:98223106 | A | G | 102 | a0001c0001t0001g0016 a0001c0001t0001g0057 a0001c0001t0001g0059 others(99): Show |
116 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.979-1878T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223106 | |||||||
| chr9:98223304 | A | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): Show |
66 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.979-2076T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223304 | |||||||
| chr9:98223428 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.979-2200G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223428 | |||||||
| chr9:98223445 | T | G | 141 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(138): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.979-2217A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223445 | |||||||
| chr9:98223544 | T | G | 10 | a0001c0001t0001g0015 a0002c0003t0001g0208 a0002c0003t0001g0237 others(7): Show |
11 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.979-2316A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223544 | |||||||
| chr9:98223608 | A | G | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.979-2380T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223608 | |||||||
| chr9:98223640 | GAGTT | G | 143 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(140): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.979-2416_979-2413d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223640 | |||||||
| chr9:98223789 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.979-2561G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223789 | |||||||
| chr9:98223884 | C | A | 6 | a0003c0004t0001g0060 a0003c0004t0001g0276 a0003c0004t0001g0283 others(3): Show |
6 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-2656G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223884 | |||||||
| chr9:98223918 | G | A | 1 | a0021c0027t0001g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979-2690C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223918 | |||||||
| chr9:98223921 | C | T | 1 | a0019c0021t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979-2693G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223921 | |||||||
| chr9:98223974 | C | T | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-2746G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223974 | |||||||
| chr9:98224015 | T | C | 162 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.979-2787A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224015 | |||||||
| chr9:98224060 | C | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.979-2832G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224060 | |||||||
| chr9:98224072 | T | C | 3 | a0001c0002t0001g0315 a0001c0002t0001g0316 a0001c0002t0001g0317 |
3 | NA18966.hp2 NA18967.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.979-2844A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224072 | |||||||
| chr9:98224154 | A | G | 7 | a0005c0010t0001g0037 a0005c0010t0001g0038 a0005c0010t0001g0040 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-2926T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224154 | |||||||
| chr9:98224166 | T | C | 7 | a0005c0010t0001g0037 a0005c0010t0001g0038 a0005c0010t0001g0040 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-2938A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224166 | |||||||
| chr9:98224176 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.979-2948C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224176 | |||||||
| chr9:98224183 | C | T | 5 | a0001c0002t0001g0147 a0001c0002t0001g0149 a0001c0002t0001g0150 others(2): Show |
5 | HG00544.hp2 HG02074.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-2955G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224183 | |||||||
| chr9:98224207 | A | G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(148): Show |
163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.979-2979T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224207 | |||||||
| chr9:98224210 | AG | A | 154 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.979-2983delC | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224210 | |||||||
| chr9:98224218 | A | AAAG | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-2993_979-2991d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224218 | |||||||
| chr9:98224265 | GT | G | 149 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.979-3038delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224265 | |||||||
| chr9:98224275 | CTTTTCTT others(12): Show |
C | 1 | a0003c0004t0001g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.979-3066_979-3048d others(21): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224275 | |||||||
| chr9:98224280 | C | CT | 57 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0061 others(54): Show |
59 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.979-3053dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224280 | |||||||
| chr9:98224280 | CT | C | 34 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0105 others(31): Show |
35 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.979-3053delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224280 | |||||||
| chr9:98224280 | CTTT | C | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-3055_979-3053d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224280 | |||||||
| chr9:98224285 | T | C | 2 | a0002c0003t0001g0212 a0011c0040t0001g0143 |
2 | HG00597.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.979-3057A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224285 | |||||||
| chr9:98224374 | C | A | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-3146G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224374 | |||||||
| chr9:98224411 | T | C | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-3183A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224411 | |||||||
| chr9:98224565 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.979-3337C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224565 | |||||||
| chr9:98224722 | G | A | 1 | a0003c0004t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.979-3494C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224722 | |||||||
| chr9:98224908 | C | A | 5 | a0002c0003t0001g0208 a0002c0003t0001g0237 a0002c0003t0001g0238 others(2): Show |
5 | HG00733.hp1 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-3680G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224908 | |||||||
| chr9:98225085 | C | T | 3 | a0001c0002t0001g0312 a0001c0002t0001g0313 a0001c0002t0001g0314 |
3 | NA18959.hp2 NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.979-3857G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225085 | |||||||
| chr9:98225172 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.978+3780C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225172 | |||||||
| chr9:98225265 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
6 | HG00639.hp2 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+3687C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225265 | |||||||
| chr9:98225340 | A | G | 138 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(135): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.978+3612T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225340 | |||||||
| chr9:98225434 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.978+3518T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225434 | |||||||
| chr9:98225444 | T | C | 4 | a0002c0003t0001g0269 a0002c0003t0001g0310 a0018c0029t0001g0261 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+3508A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225444 | |||||||
| chr9:98225561 | C | A | 314 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(311): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.978+3391G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225561 | |||||||
| chr9:98225608 | T | C | 139 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(136): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+3344A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225608 | |||||||
| chr9:98225635 | G | C | 8 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+3317C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225635 | |||||||
| chr9:98225642 | T | C | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+3310A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225642 | |||||||
| chr9:98225735 | G | A | 1 | a0014c0031t0001g0246 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.978+3217C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225735 | |||||||
| chr9:98225785 | T | C | 139 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(136): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+3167A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225785 | |||||||
| chr9:98225874 | G | A | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+3078C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225874 | |||||||
| chr9:98225882 | C | T | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.978+3070G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225882 | |||||||
| chr9:98225925 | T | A | 3 | a0003c0009t0001g0035 a0005c0015t0001g0033 a0005c0015t0001g0034 |
3 | HG01884.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.978+3027A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225925 | |||||||
| chr9:98226071 | C | A | 3 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0183 |
3 | NA18951.hp1 NA18953.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.978+2881G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226071 | |||||||
| chr9:98226195 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(37): Show |
43 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.978+2757C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226195 | |||||||
| chr9:98226220 | T | C | 2 | a0006c0016t0001g0051 a0006c0016t0001g0052 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.978+2732A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226220 | |||||||
| chr9:98226228 | G | A | 139 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(136): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+2724C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226228 | |||||||
| chr9:98226264 | C | T | 1 | a0006c0038t0001g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.978+2688G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226264 | |||||||
| chr9:98226303 | C | T | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2649G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226303 | |||||||
| chr9:98226317 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.978+2635C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226317 | |||||||
| chr9:98226365 | A | G | 1 | a0002c0003t0001g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.978+2587T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226365 | |||||||
| chr9:98226393 | G | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2559C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226393 | |||||||
| chr9:98226527 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.978+2425A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226527 | |||||||
| chr9:98226630 | G | A | 1 | a0002c0003t0001g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.978+2322C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226630 | |||||||
| chr9:98226679 | T | C | 4 | a0002c0003t0001g0269 a0002c0003t0001g0310 a0018c0029t0001g0261 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2273A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226679 | |||||||
| chr9:98226907 | G | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2045C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226907 | |||||||
| chr9:98226922 | G | A | 1 | a0001c0002t0001g0119 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.978+2030C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226922 | |||||||
| chr9:98226987 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.978+1965A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226987 | |||||||
| chr9:98227166 | T | G | 1 | a0021c0027t0001g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.978+1786A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227166 | |||||||
| chr9:98227284 | G | A | 1 | a0002c0003t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.978+1668C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227284 | |||||||
| chr9:98227355 | C | T | 1 | a0003c0004t0001g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978+1597G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227355 | |||||||
| chr9:98227400 | C | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+1552G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227400 | |||||||
| chr9:98227485 | G | A | 1 | a0003c0004t0001g0278 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.978+1467C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227485 | |||||||
| chr9:98227554 | C | T | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.978+1398G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227554 | |||||||
| chr9:98227614 | A | AC | 140 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(137): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.978+1337dupG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227614 | |||||||
| chr9:98227781 | CA | C | 117 | a0001c0001t0001g0205 a0002c0003t0001g0005 a0002c0003t0001g0006 others(114): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.978+1170delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227781 | |||||||
| chr9:98227781 | CAA | C | 16 | a0002c0003t0001g0010 a0002c0003t0001g0021 a0002c0003t0001g0211 others(13): Show |
19 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+1169_978+1170d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227781 | |||||||
| chr9:98228012 | G | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+940C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228012 | |||||||
| chr9:98228075 | C | T | 1 | a0003c0004t0001g0300 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.978+877G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228075 | |||||||
| chr9:98228298 | A | C | 61 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(58): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.978+654T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228298 | |||||||
| chr9:98228571 | G | A | 76 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(73): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.978+381C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228571 | |||||||
| chr9:98228603 | C | T | 1 | a0001c0002t0001g0147 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.978+349G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228603 | |||||||
| chr9:98228631 | A | C | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+321T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228631 | |||||||
| chr9:98228702 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.978+250A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228702 | |||||||
| chr9:98228815 | T | C | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.978+137A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228815 | |||||||
| chr9:98228820 | A | C | 8 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+132T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228820 | |||||||
| chr9:98229572 | A | C | 2 | a0006c0016t0001g0051 a0006c0016t0001g0052 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.782-424T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229572 | |||||||
| chr9:98229654 | G | A | 1 | a0005c0010t0001g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.782-506C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229654 | |||||||
| chr9:98229655 | C | A | 1 | a0005c0010t0001g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.782-507G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229655 | |||||||
| chr9:98229936 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0118 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-788C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229936 | |||||||
| chr9:98229944 | C | T | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.782-796G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229944 | |||||||
| chr9:98230247 | GA | G | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.782-1100delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230247 | |||||||
| chr9:98230334 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.782-1186G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230334 | |||||||
| chr9:98230413 | C | T | 140 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(137): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.782-1265G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230413 | |||||||
| chr9:98230540 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.782-1392C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230540 | |||||||
| chr9:98230612 | C | T | 7 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(4): Show |
7 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-1464G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230612 | |||||||
| chr9:98230651 | G | C | 45 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(42): Show |
51 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.782-1503C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230651 | |||||||
| chr9:98230740 | C | CT | 227 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.782-1593_782-1592i others(3): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230740 | |||||||
| chr9:98230829 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.782-1681G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230829 | |||||||
| chr9:98230963 | C | T | 11 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.782-1815G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230963 | |||||||
| chr9:98231033 | T | C | 1 | a0002c0003t0001g0209 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.782-1885A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231033 | |||||||
| chr9:98231171 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.782-2023T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231171 | |||||||
| chr9:98231178 | C | T | 62 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(59): Show |
74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.782-2030G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231178 | |||||||
| chr9:98231279 | C | CT | 72 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0057 others(69): Show |
77 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.782-2132dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | |||||||
| chr9:98231279 | C | CTT | 29 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(26): Show |
33 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.782-2133_782-2132d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | |||||||
| chr9:98231279 | C | CTTT | 40 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0191 others(37): Show |
44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.781+2134_782-2132d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | |||||||
| chr9:98231279 | C | CTTTT | 8 | a0003c0004t0001g0060 a0003c0004t0001g0273 a0003c0004t0001g0287 others(5): Show |
8 | HG01109.hp2 HG02723.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.781+2133_782-2132d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | |||||||
| chr9:98231279 | CT | C | 49 | a0001c0001t0001g0204 a0001c0002t0001g0127 a0002c0003t0001g0006 others(46): Show |
56 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.782-2132delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | |||||||
| chr9:98231279 | CTTTTTTT others(2): Show |
C | 12 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(9): Show |
12 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.781+2128_782-2132d others(11): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | |||||||
| chr9:98231325 | T | C | 1 | a0002c0003t0001g0255 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.781+2091A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231325 | |||||||
| chr9:98231391 | T | C | 8 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.781+2025A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231391 | |||||||
| chr9:98231419 | C | G | 1 | a0009c0013t0001g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.781+1997G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231419 | |||||||
| chr9:98231687 | T | C | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+1729A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231687 | |||||||
| chr9:98231705 | C | T | 1 | a0002c0003t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781+1711G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231705 | |||||||
| chr9:98231707 | T | C | 14 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(11): Show |
14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.781+1709A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231707 | |||||||
| chr9:98232176 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781+1240T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232176 | |||||||
| chr9:98232188 | G | A | 62 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(59): Show |
74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.781+1228C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232188 | |||||||
| chr9:98232194 | G | C | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+1222C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232194 | |||||||
| chr9:98232227 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.781+1189C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232227 | |||||||
| chr9:98232236 | G | A | 2 | a0003c0011t0001g0032 a0003c0034t0001g0050 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.781+1180C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232236 | |||||||
| chr9:98232340 | C | CTGTTTTT others(5): Show |
2 | a0002c0003t0001g0220 a0018c0029t0001g0261 |
2 | HG03098.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.781+1064_781+1075d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232340 | |||||||
| chr9:98232342 | G | GT | 6 | a0001c0001t0001g0073 a0001c0001t0001g0176 a0001c0001t0001g0197 others(3): Show |
7 | HG00140.hp1 HG01069.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+1073dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTGTTTTT others(11): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18985.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.781+1073_781+1074i others(20): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(6): Show |
1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781+1073_781+1074i others(15): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(7): Show |
9 | a0003c0009t0001g0036 a0003c0009t0001g0039 a0003c0009t0001g0043 others(6): Show |
9 | HG01255.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(16): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(8): Show |
3 | a0003c0009t0001g0035 a0005c0015t0001g0033 a0005c0015t0001g0034 |
3 | HG01884.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.781+1073_781+1074i others(17): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(9): Show |
12 | a0003c0004t0001g0048 a0003c0004t0001g0290 a0003c0004t0001g0300 others(9): Show |
12 | HG01081.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(18): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(10): Show |
38 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0064 others(35): Show |
41 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(19): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(11): Show |
55 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
65 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(20): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(12): Show |
22 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0069 others(19): Show |
22 | HG01099.hp2 HG01109.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(21): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232342 | G | GTTTTTTT others(13): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0088 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.781+1073_781+1074i others(22): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | |||||||
| chr9:98232343 | T | TTTTTTTT others(4): Show |
74 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(71): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.781+1062_781+1072d others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232343 | |||||||
| chr9:98232343 | T | TTTTTTTT others(5): Show |
1 | a0002c0003t0001g0219 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.781+1072_781+1073i others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232343 | |||||||
| chr9:98232360 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.781+1056C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232360 | |||||||
| chr9:98232368 | C | T | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781+1048G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232368 | |||||||
| chr9:98232385 | T | C | 42 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(39): Show |
46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.781+1031A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232385 | |||||||
| chr9:98232394 | A | G | 11 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.781+1022T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232394 | |||||||
| chr9:98232441 | T | C | 140 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(137): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.781+975A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232441 | |||||||
| chr9:98232490 | T | A | 11 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.781+926A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232490 | |||||||
| chr9:98232521 | T | C | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.781+895A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232521 | |||||||
| chr9:98232614 | A | G | 63 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(60): Show |
67 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.781+802T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232614 | |||||||
| chr9:98232799 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.781+617A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232799 | |||||||
| chr9:98233059 | G | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+357C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233059 | |||||||
| chr9:98233169 | A | G | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+247T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233169 | |||||||
| chr9:98233188 | T | C | 2 | a0001c0002t0001g0141 a0001c0002t0001g0142 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.781+228A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233188 | |||||||
| chr9:98233252 | C | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+164G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233252 | |||||||
| chr9:98233263 | G | A | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781+153C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233263 | |||||||
| chr9:98233267 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | HG02683.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+149G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233267 | |||||||
| chr9:98233336 | C | T | 7 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(4): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+80G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233336 | |||||||
| chr9:98233337 | G | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18980.hp2 NA18992.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.781+79C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233337 | |||||||
| chr9:98233367 | C | T | 5 | a0002c0003t0001g0021 a0002c0003t0001g0219 a0002c0003t0001g0260 others(2): Show |
9 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.781+49G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233367 | |||||||
| chr9:98233590 | T | C | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-41A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233590 | |||||||
| chr9:98233650 | A | G | 1 | a0004c0005t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.648-101T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233650 | |||||||
| chr9:98233717 | T | C | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.648-168A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233717 | |||||||
| chr9:98233736 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(35): Show |
44 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.648-187A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233736 | |||||||
| chr9:98233800 | T | C | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-251A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233800 | |||||||
| chr9:98233993 | T | C | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-444A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233993 | |||||||
| chr9:98234155 | G | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-606C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234155 | |||||||
| chr9:98234181 | T | A | 1 | a0001c0002t0001g0131 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.648-632A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234181 | |||||||
| chr9:98234578 | C | T | 61 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(58): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.648-1029G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234578 | |||||||
| chr9:98234674 | G | A | 14 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(11): Show |
14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.648-1125C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234674 | |||||||
| chr9:98234706 | G | A | 43 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(40): Show |
47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-1157C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234706 | |||||||
| chr9:98234712 | C | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.648-1163G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234712 | |||||||
| chr9:98234830 | C | T | 43 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(40): Show |
47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-1281G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234830 | |||||||
| chr9:98234874 | G | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-1325C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234874 | |||||||
| chr9:98234934 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0120 |
2 | HG00741.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.648-1385C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234934 | |||||||
| chr9:98235073 | G | A | 43 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(40): Show |
47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-1524C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235073 | |||||||
| chr9:98235125 | C | T | 6 | a0003c0004t0001g0011 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
8 | HG02109.hp2 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1576G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235125 | |||||||
| chr9:98235154 | G | A | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-1605C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235154 | |||||||
| chr9:98235629 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.648-2080G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235629 | |||||||
| chr9:98235734 | T | A | 5 | a0002c0003t0001g0005 a0002c0003t0001g0212 a0002c0003t0001g0213 others(2): Show |
8 | NA18947.hp1 NA18968.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.648-2185A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235734 | |||||||
| chr9:98235830 | C | T | 14 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(11): Show |
14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.648-2281G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235830 | |||||||
| chr9:98235844 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(42): Show |
51 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.648-2295G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235844 | |||||||
| chr9:98235848 | C | T | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.648-2299G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235848 | |||||||
| chr9:98235867 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.648-2318A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235867 | |||||||
| chr9:98235966 | T | C | 11 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-2417A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235966 | |||||||
| chr9:98235983 | C | T | 1 | a0003c0012t0001g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.648-2434G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235983 | |||||||
| chr9:98235992 | G | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-2443C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235992 | |||||||
| chr9:98236031 | A | G | 140 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(137): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.648-2482T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236031 | |||||||
| chr9:98236422 | C | T | 1 | a0002c0030t0001g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.648-2873G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236422 | |||||||
| chr9:98236882 | G | A | 1 | a0004c0005t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.648-3333C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236882 | |||||||
| chr9:98236899 | G | A | 4 | a0002c0003t0001g0269 a0002c0003t0001g0310 a0018c0029t0001g0261 others(1): Show |
4 | HG01884.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-3350C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236899 | |||||||
| chr9:98236928 | AT | A | 80 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(77): Show |
95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.648-3380delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236928 | |||||||
| chr9:98237000 | T | C | 2 | a0003c0004t0001g0296 a0003c0004t0001g0297 |
2 | HG01952.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.648-3451A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237000 | |||||||
| chr9:98237036 | G | C | 43 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(40): Show |
47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-3487C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237036 | |||||||
| chr9:98237042 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.648-3493T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237042 | |||||||
| chr9:98237107 | C | T | 2 | a0003c0036t0001g0274 a0006c0035t0001g0282 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.648-3558G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237107 | |||||||
| chr9:98237161 | A | G | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-3612T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237161 | |||||||
| chr9:98237166 | G | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-3617C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237166 | |||||||
| chr9:98237303 | C | T | 1 | a0004c0005t0001g0263 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.648-3754G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237303 | |||||||
| chr9:98237344 | CA | C | 78 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(75): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.648-3796delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237344 | |||||||
| chr9:98237382 | C | T | 140 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(137): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.648-3833G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237382 | |||||||
| chr9:98237545 | C | T | 1 | a0003c0009t0001g0039 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.648-3996G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237545 | |||||||
| chr9:98237546 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.648-3997C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237546 | |||||||
| chr9:98237668 | G | A | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.648-4119C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237668 | |||||||
| chr9:98237833 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.648-4284T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237833 | |||||||
| chr9:98237860 | G | A | 1 | a0022c0041t0001g0108 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.648-4311C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237860 | |||||||
| chr9:98237870 | T | C | 1 | a0003c0004t0003g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.648-4321A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237870 | |||||||
| chr9:98237909 | CT | C | 63 | a0001c0001t0001g0159 a0001c0002t0001g0142 a0001c0002t0001g0168 others(60): Show |
75 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.648-4361delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237909 | |||||||
| chr9:98237953 | G | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-4404C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237953 | |||||||
| chr9:98238006 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.648-4457G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238006 | |||||||
| chr9:98238007 | GATTCTCC others(812): Show |
G | 59 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(56): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.647+5168_648-4459d others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238007 | |||||||
| chr9:98238050 | T | C | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.648-4501A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238050 | |||||||
| chr9:98238226 | T | C | 79 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(76): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.648-4677A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238226 | |||||||
| chr9:98238404 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.648-4855A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238404 | |||||||
| chr9:98238729 | G | GT | 7 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(4): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.648-5181dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238729 | |||||||
| chr9:98238842 | C | A | 2 | a0003c0004t0001g0299 a0003c0004t0001g0300 |
2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.647+5152G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238842 | |||||||
| chr9:98238871 | T | C | 69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.647+5123A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238871 | |||||||
| chr9:98238875 | A | C | 7 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(4): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.647+5119T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238875 | |||||||
| chr9:98239224 | A | T | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+4770T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239224 | |||||||
| chr9:98239335 | G | T | 2 | a0003c0004t0001g0284 a0003c0004t0001g0285 |
2 | HG00408.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.647+4659C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239335 | |||||||
| chr9:98239345 | G | A | 1 | a0002c0003t0001g0240 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.647+4649C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239345 | |||||||
| chr9:98239761 | A | ATATT | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+4229_647+4232d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239761 | |||||||
| chr9:98239798 | T | C | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+4196A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239798 | |||||||
| chr9:98239865 | G | T | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+4129C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239865 | |||||||
| chr9:98239889 | G | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(44): Show |
53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+4105C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239889 | |||||||
| chr9:98240153 | G | A | 15 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(12): Show |
18 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.647+3841C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240153 | |||||||
| chr9:98240164 | GTGGT | G | 8 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+3826_647+3829d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240164 | |||||||
| chr9:98240166 | G | GGT | 15 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0002t0001g0003 others(12): Show |
15 | HG00140.hp1 HG00735.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.647+3826_647+3827d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | G | GGTGT | 6 | a0002c0014t0001g0012 a0003c0004t0003g0049 a0003c0034t0001g0050 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+3824_647+3827d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | G | GGTGTGT | 36 | a0002c0030t0001g0241 a0003c0004t0001g0011 a0003c0004t0001g0024 others(33): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.647+3822_647+3827d others(8): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | G | GGTGTGTG others(1): Show |
69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
79 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.647+3820_647+3827d others(10): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | G | GGTGTGTG others(3): Show |
7 | a0002c0003t0001g0023 a0002c0003t0001g0237 a0002c0003t0001g0243 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+3818_647+3827d others(12): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | G | GGTGTGTG others(5): Show |
2 | a0002c0003t0001g0224 a0002c0003t0001g0256 |
2 | NA18945.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.647+3816_647+3827d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | GGT | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(42): Show |
51 | HG00642.hp2 HG00673.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.647+3826_647+3827d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | GGTGT | G | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+3824_647+3827d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240166 | GGTGTGT | G | 8 | a0002c0003t0001g0269 a0002c0003t0001g0310 a0003c0004t0001g0048 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+3822_647+3827d others(8): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | |||||||
| chr9:98240257 | G | C | 60 | a0002c0030t0001g0241 a0003c0004t0001g0011 a0003c0004t0001g0024 others(57): Show |
64 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.647+3737C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240257 | |||||||
| chr9:98240280 | C | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(44): Show |
53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+3714G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240280 | |||||||
| chr9:98240352 | T | A | 77 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(74): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.647+3642A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240352 | |||||||
| chr9:98240368 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18980.hp2 NA18992.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.647+3626C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240368 | |||||||
| chr9:98240503 | T | G | 1 | a0003c0004t0003g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.647+3491A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240503 | |||||||
| chr9:98240586 | T | C | 15 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(12): Show |
18 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.647+3408A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240586 | |||||||
| chr9:98240829 | C | A | 2 | a0003c0004t0001g0296 a0003c0004t0001g0297 |
2 | HG01952.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.647+3165G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240829 | |||||||
| chr9:98241007 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.647+2987G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241007 | |||||||
| chr9:98241104 | T | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(38): Show |
44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.647+2890A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241104 | |||||||
| chr9:98241163 | C | T | 3 | a0005c0010t0001g0038 a0005c0010t0001g0040 a0005c0010t0001g0041 |
3 | HG02559.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.647+2831G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241163 | |||||||
| chr9:98241168 | T | C | 1 | a0003c0004t0003g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.647+2826A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241168 | |||||||
| chr9:98241176 | A | C | 1 | a0011c0040t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.647+2818T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241176 | |||||||
| chr9:98241778 | C | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+2216G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241778 | |||||||
| chr9:98241849 | C | T | 2 | a0003c0011t0001g0032 a0003c0034t0001g0050 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.647+2145G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241849 | |||||||
| chr9:98241900 | C | T | 12 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(9): Show |
12 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.647+2094G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241900 | |||||||
| chr9:98241904 | G | C | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+2090C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241904 | |||||||
| chr9:98242179 | C | T | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+1815G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242179 | |||||||
| chr9:98242180 | G | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(44): Show |
53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+1814C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242180 | |||||||
| chr9:98242206 | C | T | 2 | a0001c0002t0001g0132 a0001c0002t0001g0166 |
2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.647+1788G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242206 | |||||||
| chr9:98242269 | A | G | 138 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(135): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.647+1725T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242269 | |||||||
| chr9:98242297 | C | T | 7 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(4): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.647+1697G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242297 | |||||||
| chr9:98242370 | A | G | 313 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(310): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.647+1624T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242370 | |||||||
| chr9:98242386 | A | G | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+1608T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242386 | |||||||
| chr9:98242441 | CA | C | 8 | a0001c0001t0001g0080 a0001c0008t0001g0121 a0001c0008t0001g0122 others(5): Show |
8 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+1552delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242441 | |||||||
| chr9:98242525 | G | C | 6 | a0001c0008t0001g0121 a0001c0008t0001g0122 a0001c0008t0001g0123 others(3): Show |
6 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+1469C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242525 | |||||||
| chr9:98242745 | G | A | 226 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(223): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.647+1249C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242745 | |||||||
| chr9:98242751 | C | G | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+1243G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242751 | |||||||
| chr9:98242803 | C | CT | 45 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0067 others(42): Show |
49 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.647+1190dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | C | CTT | 12 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0110 others(9): Show |
12 | HG00621.hp2 HG00741.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.647+1189_647+1190d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | C | CTTT | 27 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0080 others(24): Show |
31 | HG00558.hp2 HG00642.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.647+1188_647+1190d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | C | CTTTT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0085 others(28): Show |
35 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.647+1187_647+1190d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | C | CTTTTT | 20 | a0003c0004t0001g0011 a0003c0004t0001g0270 a0003c0004t0001g0275 others(17): Show |
22 | HG00280.hp1 HG00408.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.647+1186_647+1190d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | C | CTTTTTTT others(4): Show |
1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+1180_647+1190d others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | CTTTT | C | 11 | a0002c0003t0001g0211 a0003c0009t0001g0035 a0003c0009t0001g0036 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.647+1187_647+1190d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | CTTTTT | C | 6 | a0002c0003t0001g0210 a0002c0003t0001g0215 a0002c0003t0001g0217 others(3): Show |
6 | HG01361.hp1 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+1186_647+1190d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | CTTTTTT | C | 55 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(52): Show |
67 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.647+1185_647+1190d others(8): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98242803 | CTTTTTTT | C | 17 | a0002c0003t0001g0244 a0002c0003t0001g0260 a0002c0003t0001g0269 others(14): Show |
20 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.647+1184_647+1190d others(9): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | |||||||
| chr9:98243008 | G | A | 69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.647+986C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243008 | |||||||
| chr9:98243069 | G | C | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+925C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243069 | |||||||
| chr9:98243161 | C | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+833G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243161 | |||||||
| chr9:98243210 | G | C | 12 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(9): Show |
12 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.647+784C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243210 | |||||||
| chr9:98243250 | A | G | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+744T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243250 | |||||||
| chr9:98243260 | C | A | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+734G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243260 | |||||||
| chr9:98243263 | C | G | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+731G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243263 | |||||||
| chr9:98243265 | C | G | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+729G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243265 | |||||||
| chr9:98243326 | C | T | 1 | a0004c0005t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.647+668G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243326 | |||||||
| chr9:98243353 | G | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+641C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243353 | |||||||
| chr9:98243354 | T | C | 1 | a0002c0003t0001g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.647+640A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243354 | |||||||
| chr9:98243453 | C | T | 8 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+541G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243453 | |||||||
| chr9:98243454 | G | A | 1 | a0002c0007t0001g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.647+540C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243454 | |||||||
| chr9:98243463 | G | A | 2 | a0002c0003t0001g0243 a0002c0003t0001g0244 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.647+531C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243463 | |||||||
| chr9:98243534 | A | AT | 64 | a0001c0002t0001g0128 a0001c0002t0001g0129 a0001c0002t0002g0026 others(61): Show |
76 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.647+459dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243534 | |||||||
| chr9:98243534 | A | ATT | 16 | a0002c0003t0001g0215 a0002c0003t0001g0216 a0002c0003t0001g0260 others(13): Show |
19 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.647+458_647+459dup others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243534 | |||||||
| chr9:98243534 | AT | A | 48 | a0001c0001t0001g0114 a0001c0002t0001g0161 a0003c0004t0001g0011 others(45): Show |
52 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.647+459delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243534 | |||||||
| chr9:98243570 | CTT | C | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.647+422_647+423del others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243570 | |||||||
| chr9:98243571 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.647+423A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243571 | |||||||
| chr9:98243613 | T | C | 1 | a0003c0004t0001g0298 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.647+381A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243613 | |||||||
| chr9:98243733 | C | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(38): Show |
44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.647+261G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243733 | |||||||
| chr9:98243780 | G | A | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.647+214C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243780 | |||||||
| chr9:98243928 | T | C | 78 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(75): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.647+66A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243928 | |||||||
| chr9:98243934 | A | G | 137 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(134): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.647+60T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243934 | |||||||
| chr9:98243959 | A | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0201 |
2 | NA18953.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.647+35T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243959 | |||||||
| chr9:98243984 | T | C | 1 | a0001c0006t0001g0019 | 2 | NA18945.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.647+10A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243984 | |||||||
| chr9:98244154 | C | A | 138 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(135): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.512-25G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244154 | |||||||
| chr9:98244161 | T | C | 226 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(223): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.512-32A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244161 | |||||||
| chr9:98244208 | C | T | 5 | a0002c0003t0001g0005 a0002c0003t0001g0212 a0002c0003t0001g0213 others(2): Show |
8 | NA18947.hp1 NA18968.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-79G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244208 | |||||||
| chr9:98244387 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.512-258C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244387 | |||||||
| chr9:98244413 | A | C | 138 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(135): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.512-284T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244413 | |||||||
| chr9:98244573 | C | T | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-444G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244573 | |||||||
| chr9:98244596 | T | C | 2 | a0001c0006t0001g0018 a0001c0006t0001g0162 |
3 | HG01993.hp1 HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.512-467A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244596 | |||||||
| chr9:98244600 | A | G | 1 | a0003c0011t0001g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-471T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244600 | |||||||
| chr9:98244613 | C | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(38): Show |
44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.512-484G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244613 | |||||||
| chr9:98244640 | C | A | 2 | a0001c0019t0001g0163 a0001c0019t0001g0164 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.512-511G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244640 | |||||||
| chr9:98244659 | C | CA | 38 | a0001c0001t0001g0057 a0001c0001t0001g0074 a0001c0001t0001g0076 others(35): Show |
41 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.512-531dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | |||||||
| chr9:98244659 | C | CAA | 10 | a0002c0003t0001g0212 a0002c0003t0001g0269 a0002c0003t0001g0310 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.512-532_512-531dup others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | |||||||
| chr9:98244659 | C | CAAA | 56 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(53): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.512-533_512-531dup others(3): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | |||||||
| chr9:98244659 | C | CAAAA | 12 | a0001c0001t0001g0110 a0002c0003t0001g0023 a0002c0003t0001g0210 others(9): Show |
13 | HG01361.hp1 HG01433.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.512-534_512-531dup others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | |||||||
| chr9:98244659 | CA | C | 50 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0064 others(47): Show |
55 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.512-531delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | |||||||
| chr9:98244688 | G | C | 62 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(59): Show |
74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.512-559C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244688 | |||||||
| chr9:98244695 | A | G | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-566T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244695 | |||||||
| chr9:98244992 | G | C | 8 | a0004c0005t0001g0081 a0004c0005t0001g0082 a0004c0005t0001g0263 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.512-863C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244992 | |||||||
| chr9:98245000 | G | A | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.512-871C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245000 | |||||||
| chr9:98245390 | A | G | 2 | a0002c0003t0001g0209 a0002c0003t0001g0210 |
2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.512-1261T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245390 | |||||||
| chr9:98245488 | G | A | 58 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(55): Show |
69 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.512-1359C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245488 | |||||||
| chr9:98245514 | C | T | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-1385G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245514 | |||||||
| chr9:98245517 | A | G | 47 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(44): Show |
53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.512-1388T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245517 | |||||||
| chr9:98245595 | G | A | 77 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.512-1466C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245595 | |||||||
| chr9:98245990 | T | C | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-1861A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245990 | |||||||
| chr9:98246259 | C | T | 233 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(230): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.512-2130G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246259 | |||||||
| chr9:98246300 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.512-2171C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246300 | |||||||
| chr9:98246603 | A | G | 138 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(135): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.512-2474T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246603 | |||||||
| chr9:98246672 | C | T | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-2543G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246672 | |||||||
| chr9:98246769 | C | T | 136 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(133): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.512-2640G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246769 | |||||||
| chr9:98246794 | T | C | 40 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(37): Show |
44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.512-2665A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246794 | |||||||
| chr9:98246814 | G | A | 6 | a0004c0005t0001g0263 a0004c0005t0001g0264 a0004c0005t0001g0265 others(3): Show |
6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-2685C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246814 | |||||||
| chr9:98246990 | C | T | 2 | a0018c0029t0001g0261 a0021c0027t0001g0262 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.512-2861G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246990 | |||||||
| chr9:98247006 | C | T | 69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.512-2877G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247006 | |||||||
| chr9:98247007 | G | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(38): Show |
44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.512-2878C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247007 | |||||||
| chr9:98247025 | T | TA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0111 a0001c0001t0001g0120 others(4): Show |
7 | HG01192.hp1 HG02055.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.512-2897dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247025 | |||||||
| chr9:98247050 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.512-2921C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247050 | |||||||
| chr9:98247144 | G | A | 58 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(55): Show |
69 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.512-3015C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247144 | |||||||
| chr9:98247187 | C | T | 45 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(42): Show |
49 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.512-3058G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247187 | |||||||
| chr9:98247241 | C | T | 11 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-3112G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247241 | |||||||
| chr9:98247329 | CA | C | 162 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.512-3201delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247329 | |||||||
| chr9:98247362 | C | CA | 74 | a0001c0001t0001g0112 a0001c0006t0001g0019 a0002c0003t0001g0005 others(71): Show |
87 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.512-3234dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247362 | |||||||
| chr9:98247536 | A | G | 75 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(72): Show |
90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.512-3407T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247536 | |||||||
| chr9:98247661 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18980.hp2 NA18992.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.512-3532C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247661 | |||||||
| chr9:98247724 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.512-3595C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247724 | |||||||
| chr9:98247728 | C | CA | 21 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG00621.hp2 HG00741.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.512-3600dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98247728 | C | CAAAAAAA others(3): Show |
4 | a0004c0005t0001g0263 a0004c0005t0001g0265 a0004c0005t0001g0266 others(1): Show |
4 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-3609_512-3600d others(12): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98247728 | C | CAAAAAAA others(4): Show |
1 | a0004c0005t0001g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.512-3610_512-3600d others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98247728 | CA | C | 57 | a0001c0001t0001g0080 a0001c0001t0001g0186 a0001c0008t0001g0121 others(54): Show |
59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.512-3600delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98247728 | CAA | C | 5 | a0003c0004t0001g0011 a0003c0004t0001g0272 a0003c0004t0001g0273 others(2): Show |
7 | HG02280.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.512-3601_512-3600d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98247728 | CAAAA | C | 55 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(52): Show |
66 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.512-3603_512-3600d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98247728 | CAAAAA | C | 9 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(6): Show |
13 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.512-3604_512-3600d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | |||||||
| chr9:98248068 | G | A | 22 | a0003c0004t0001g0024 a0003c0004t0001g0284 a0003c0004t0001g0285 others(19): Show |
23 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.511+3717C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248068 | |||||||
| chr9:98248153 | A | G | 1 | a0004c0005t0001g0263 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.511+3632T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248153 | |||||||
| chr9:98248260 | C | T | 6 | a0004c0005t0001g0263 a0004c0005t0001g0264 a0004c0005t0001g0265 others(3): Show |
6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+3525G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248260 | |||||||
| chr9:98248422 | G | T | 48 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(45): Show |
54 | HG00140.hp2 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.511+3363C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248422 | |||||||
| chr9:98248462 | C | T | 2 | a0007c0018t0001g0078 a0007c0018t0001g0079 |
2 | HG01071.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.511+3323G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248462 | |||||||
| chr9:98248524 | C | T | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(37): Show |
43 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.511+3261G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248524 | |||||||
| chr9:98248847 | T | G | 20 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(17): Show |
20 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.511+2938A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248847 | |||||||
| chr9:98248868 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.511+2917C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248868 | |||||||
| chr9:98248925 | A | C | 1 | a0003c0004t0001g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.511+2860T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248925 | |||||||
| chr9:98249031 | C | A | 69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.511+2754G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249031 | |||||||
| chr9:98249065 | G | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0305 a0003c0004t0001g0306 |
4 | HG02809.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+2720C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249065 | |||||||
| chr9:98249076 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.511+2709G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249076 | |||||||
| chr9:98249270 | C | T | 42 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(39): Show |
46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.511+2515G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249270 | |||||||
| chr9:98249350 | C | T | 2 | a0009c0013t0001g0028 a0009c0013t0001g0029 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.511+2435G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249350 | |||||||
| chr9:98249407 | C | T | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+2378G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249407 | |||||||
| chr9:98249534 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.511+2251G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249534 | |||||||
| chr9:98249714 | T | C | 2 | a0003c0009t0001g0043 a0016c0025t0001g0042 |
2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.511+2071A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249714 | |||||||
| chr9:98249743 | T | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0056 others(18): Show |
22 | HG00558.hp1 HG01099.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.511+2042A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249743 | |||||||
| chr9:98249993 | G | A | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+1792C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249993 | |||||||
| chr9:98250033 | C | T | 1 | a0002c0003t0001g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.511+1752G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250033 | |||||||
| chr9:98250055 | G | A | 1 | a0002c0003t0001g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511+1730C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250055 | |||||||
| chr9:98250133 | G | T | 1 | a0019c0021t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.511+1652C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250133 | |||||||
| chr9:98250233 | A | C | 1 | a0003c0004t0001g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.511+1552T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250233 | |||||||
| chr9:98250312 | A | G | 137 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(134): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.511+1473T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250312 | |||||||
| chr9:98250326 | AC | A | 137 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(134): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.511+1458delG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250326 | |||||||
| chr9:98250402 | T | A | 1 | a0002c0003t0001g0257 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511+1383A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250402 | |||||||
| chr9:98250474 | GC | G | 6 | a0004c0005t0001g0263 a0004c0005t0001g0264 a0004c0005t0001g0265 others(3): Show |
6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+1310delG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250474 | |||||||
| chr9:98250542 | G | A | 69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.511+1243C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250542 | |||||||
| chr9:98250688 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.511+1097A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250688 | |||||||
| chr9:98250825 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.511+960G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250825 | |||||||
| chr9:98250865 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.511+920C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250865 | |||||||
| chr9:98250896 | T | G | 58 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(55): Show |
69 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.511+889A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250896 | |||||||
| chr9:98251106 | G | A | 15 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(12): Show |
15 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.511+679C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251106 | |||||||
| chr9:98251121 | C | T | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.511+664G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251121 | |||||||
| chr9:98251145 | C | T | 1 | a0003c0004t0003g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511+640G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251145 | |||||||
| chr9:98251149 | G | A | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+636C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251149 | |||||||
| chr9:98251156 | G | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+629C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251156 | |||||||
| chr9:98251157 | T | C | 69 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(66): Show |
84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.511+628A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251157 | |||||||
| chr9:98251216 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.511+569C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251216 | |||||||
| chr9:98251235 | G | A | 15 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(12): Show |
15 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.511+550C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251235 | |||||||
| chr9:98251276 | G | A | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+509C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251276 | |||||||
| chr9:98251290 | C | CA | 7 | a0002c0014t0001g0012 a0003c0004t0001g0048 a0003c0004t0003g0049 others(4): Show |
8 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.511+494dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251290 | |||||||
| chr9:98251366 | T | G | 1 | a0001c0002t0001g0207 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.511+419A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251366 | |||||||
| chr9:98251560 | C | G | 90 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0010 others(87): Show |
105 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.511+225G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251560 | |||||||
| chr9:98251561 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.511+224T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251561 | |||||||
| chr9:98252033 | G | GA | 63 | a0001c0001t0001g0258 a0002c0003t0001g0005 a0002c0003t0001g0006 others(60): Show |
75 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.370-108dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252033 | |||||||
| chr9:98252036 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.370-110T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252036 | |||||||
| chr9:98252089 | C | G | 21 | a0003c0004t0001g0048 a0003c0004t0003g0049 a0003c0009t0001g0035 others(18): Show |
21 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.370-163G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252089 | |||||||
| chr9:98252168 | T | C | 1 | a0003c0026t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.370-242A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252168 | |||||||
| chr9:98252169 | C | T | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.370-243G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252169 | |||||||
| chr9:98252227 | A | G | 2 | a0018c0029t0001g0261 a0021c0027t0001g0262 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.370-301T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252227 | |||||||
| chr9:98252542 | C | T | 11 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-616G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252542 | |||||||
| chr9:98252678 | CTAGTCCC others(2): Show |
C | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-761_370-753del others(9): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252678 | |||||||
| chr9:98252688 | A | C | 3 | a0002c0003t0001g0260 a0002c0007t0001g0007 a0002c0007t0001g0259 |
6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-762T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252688 | |||||||
| chr9:98252770 | C | A | 5 | a0003c0004t0001g0048 a0003c0004t0003g0049 a0003c0011t0001g0045 others(2): Show |
5 | HG01081.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-844G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252770 | |||||||
| chr9:98252777 | T | C | 7 | a0002c0003t0001g0260 a0002c0003t0001g0269 a0002c0003t0001g0310 others(4): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.370-851A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252777 | |||||||
| chr9:98252792 | G | A | 4 | a0003c0004t0001g0048 a0003c0011t0001g0045 a0003c0011t0001g0047 others(1): Show |
4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-866C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252792 | |||||||
| chr9:98252838 | G | A | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.370-912C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252838 | |||||||
| chr9:98253151 | T | C | 15 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(12): Show |
15 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.370-1225A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253151 | |||||||
| chr9:98253237 | G | A | 6 | a0004c0005t0001g0263 a0004c0005t0001g0264 a0004c0005t0001g0265 others(3): Show |
6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1311C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253237 | |||||||
| chr9:98253322 | C | T | 16 | a0003c0009t0001g0035 a0003c0009t0001g0036 a0003c0009t0001g0039 others(13): Show |
16 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.370-1396G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253322 | |||||||
| chr9:98253378 | A | G | 1 | a0003c0011t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.370-1452T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253378 | |||||||
| chr9:98253467 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.370-1541G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253467 | |||||||
| chr9:98253523 | G | A | 21 | a0003c0004t0001g0048 a0003c0004t0003g0049 a0003c0009t0001g0035 others(18): Show |
21 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.370-1597C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253523 | |||||||
| chr9:98253642 | T | C | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369+1531A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253642 | |||||||
| chr9:98253656 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.369+1517G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253656 | |||||||
| chr9:98253838 | G | A | 1 | a0003c0004t0003g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.369+1335C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253838 | |||||||
| chr9:98253902 | C | T | 1 | a0001c0002t0001g0054 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+1271G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253902 | |||||||
| chr9:98253981 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.369+1192C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253981 | |||||||
| chr9:98254089 | G | A | 1 | a0003c0034t0001g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369+1084C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254089 | |||||||
| chr9:98254170 | G | C | 2 | a0002c0003t0001g0269 a0002c0003t0001g0310 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.369+1003C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254170 | |||||||
| chr9:98254305 | GT | G | 41 | a0003c0004t0001g0011 a0003c0004t0001g0024 a0003c0004t0001g0025 others(38): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.369+867delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254305 | |||||||
| chr9:98254416 | T | G | 2 | a0001c0001t0001g0308 a0001c0002t0001g0307 |
2 | HG01515.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.369+757A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254416 | |||||||
| chr9:98254554 | T | C | 2 | a0006c0016t0001g0051 a0006c0016t0001g0052 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.369+619A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254554 | |||||||
| chr9:98254646 | T | G | 1 | a0002c0003t0001g0309 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.369+527A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254646 | |||||||
| chr9:98254692 | C | A | 1 | a0002c0003t0001g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+481G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254692 | |||||||
| chr9:98255017 | T | C | 1 | a0001c0002t0001g0311 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.369+156A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98255017 | |||||||
| chr9:98255089 | C | T | 21 | a0003c0004t0001g0048 a0003c0004t0003g0049 a0003c0009t0001g0035 others(18): Show |
21 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.369+84G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98255089 | |||||||
| chr9:98255149 | G | A | 6 | a0001c0002t0001g0312 a0001c0002t0001g0313 a0001c0002t0001g0314 others(3): Show |
6 | NA18959.hp2 NA18966.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+24C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98255149 |