Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23329 |
| ensemblid | ENSG00000111490.15 |
| hgncid | 29164 |
| symbol | TBC1D30 |
| name | TBC1 domain family member 30 |
| refseq_nuc | NM_015279.2 |
| refseq_prot | NP_056094.1 |
| ensembl_nuc | ENST00000539867.6 |
| ensembl_prot | ENSP00000440207.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 64824647 |
| end | 64881033 |
| strand | + |
| ver | v1.2 |
| region | chr12:64824647-64881033 |
| region5000 | chr12:64819647-64886033 |
| regionname0 | TBC1D30_chr12_64824647_64881033 |
| regionname5000 | TBC1D30_chr12_64819647_64886033 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 761 | 217 | 25 | 50 | 94 | 11 | 35 | 62 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | MRQDK others(756): Show |
chr12 | 64819647 | 64886033 |
| a0002 | 0/0 | 761 | 76 | 70 | 5 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | MRQDK others(756): Show |
chr12 | 64819647 | 64886033 |
| a0003 | 0/0 | 761 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | MRQDK others(756): Show |
chr12 | 64819647 | 64886033 |
| a0004 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | MRQDK others(756): Show |
chr12 | 64819647 | 64886033 |
| a0005 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | MRQDK others(756): Show |
chr12 | 64819647 | 64886033 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2283 | 204 | 23 | 46 | 92 | 9 | 32 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0004 | 0/0 | 2283 | 7 | 0 | 3 | 0 | 2 | 2 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0012 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0013 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0014 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0015 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0016 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0001c0017 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0002c0002 | 0/0 | 2283 | 54 | 49 | 4 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0002c0003 | 0/0 | 2283 | 10 | 10 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0002c0005 | 0/0 | 2283 | 6 | 6 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0002c0006 | 0/0 | 2283 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0002c0010 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0002c0011 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0003c0007 | 0/0 | 2283 | 3 | 0 | 0 | 0 | 1 | 2 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0004c0008 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 | ||
| a0005c0009 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | ATGCG others(2278): Show |
chr12 | 64819647 | 64886033 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7764 | 105 | 13 | 22 | 53 | 3 | 13 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0002 | 0/0 | 7764 | 15 | 3 | 2 | 2 | 3 | 5 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0003 | 1/0 | 7764 | 31 | 0 | 4 | 17 | 2 | 7 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0004 | 0/0 | 7764 | 20 | 1 | 6 | 10 | 1 | 2 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0005 | 0/0 | 7764 | 10 | 0 | 6 | 4 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0009 | 0/0 | 7764 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0011 | 0/0 | 7764 | 4 | 0 | 0 | 0 | 0 | 4 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0014 | 0/0 | 7764 | 3 | 0 | 3 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0015 | 0/0 | 7764 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0016 | 0/0 | 7764 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0017 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0018 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0022 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0023 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0001t0024 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0004t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0004t0005 | 0/0 | 7764 | 6 | 0 | 3 | 0 | 2 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0012t0026 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0013t0003 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0014t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0015t0005 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0016t0003 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0001c0017t0017 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0001 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0002 | 0/0 | 7764 | 17 | 14 | 2 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0005 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0006 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7767): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0007 | 0/0 | 7764 | 10 | 8 | 2 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0008 | 0/0 | 7764 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0010 | 0/0 | 7764 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0012 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0013 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0019 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0020 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0021 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0025 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0028 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0030 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0002t0031 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0003t0006 | 0/0 | 7772 | 10 | 10 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7767): Show |
chr12 | 64819647 | 64886033 |
| a0002c0005t0006 | 0/0 | 7772 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7767): Show |
chr12 | 64819647 | 64886033 |
| a0002c0005t0012 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0005t0027 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7767): Show |
chr12 | 64819647 | 64886033 |
| a0002c0006t0001 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0006t0002 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0002c0010t0006 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7767): Show |
chr12 | 64819647 | 64886033 |
| a0002c0011t0006 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7767): Show |
chr12 | 64819647 | 64886033 |
| a0003c0007t0001 | 0/0 | 7764 | 3 | 0 | 0 | 0 | 1 | 2 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0004c0008t0001 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| a0005c0009t0029 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | AGCCT others(7759): Show |
chr12 | 64819647 | 64886033 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0011g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0014g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0014g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0015g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0017g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0018g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0023g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0001t0024g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0004t0005g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0004t0005g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0004t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0004t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0012t0026g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0013t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0014t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0015t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0016t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0001c0017t0017g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0007g0002 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0008g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0013g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0013g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0025g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0028g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0030g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0002t0031g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0003t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0005t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0005t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0005t0012g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0005t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0005t0027g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0006t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0006t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0006t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0006t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0010t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0002c0011t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0003c0007t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0003c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0004c0008t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| a0005c0009t0029g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | GBR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | FIN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0125 | EUR | FIN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00597 | hp2 | a0001 | c0013 | t0003 | g0085 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00735 | hp1 | a0001 | c0004 | t0005 | g0186 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00738 | hp1 | a0001 | c0001 | t0023 | g0064 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0027 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01070 | hp1 | a0001 | c0001 | t0014 | g0025 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01074 | hp2 | a0001 | c0004 | t0005 | g0029 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01099 | hp2 | a0001 | c0004 | t0005 | g0205 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01106 | hp2 | a0001 | c0001 | t0017 | g0181 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01109 | hp2 | a0002 | c0002 | t0007 | g0002 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0211 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01243 | hp1 | a0002 | c0002 | t0007 | g0002 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01258 | hp2 | a0001 | c0001 | t0014 | g0025 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01261 | hp2 | a0001 | c0017 | t0017 | g0209 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01361 | hp1 | a0002 | c0006 | t0001 | g0242 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01516 | hp2 | a0001 | c0004 | t0005 | g0024 | EUR | IBS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01517 | hp1 | a0001 | c0004 | t0005 | g0024 | EUR | IBS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0189 | EUR | IBS | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01884 | hp2 | a0002 | c0006 | t0002 | g0237 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0219 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0222 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02055 | hp1 | a0002 | c0003 | t0006 | g0176 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02055 | hp2 | a0002 | c0003 | t0006 | g0004 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02135 | hp1 | a0001 | c0001 | t0022 | g0001 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0168 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02145 | hp2 | a0002 | c0003 | t0006 | g0038 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02257 | hp1 | a0002 | c0002 | t0007 | g0041 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0055 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02258 | hp2 | a0001 | c0015 | t0005 | g0087 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02280 | hp1 | a0002 | c0002 | t0013 | g0103 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02293 | hp1 | a0004 | c0008 | t0001 | g0163 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02451 | hp1 | a0002 | c0002 | t0030 | g0040 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0215 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02572 | hp1 | a0002 | c0002 | t0007 | g0044 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02572 | hp2 | a0002 | c0002 | t0008 | g0052 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0216 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02615 | hp1 | a0002 | c0002 | t0025 | g0136 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02622 | hp1 | a0002 | c0002 | t0010 | g0057 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02622 | hp2 | a0002 | c0002 | t0007 | g0045 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02630 | hp1 | a0002 | c0005 | t0012 | g0032 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02717 | hp2 | a0002 | c0002 | t0028 | g0082 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02723 | hp1 | a0002 | c0010 | t0006 | g0236 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02738 | hp1 | a0001 | c0014 | t0001 | g0047 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02809 | hp2 | a0002 | c0002 | t0008 | g0170 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02818 | hp1 | a0005 | c0009 | t0029 | g0241 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02818 | hp2 | a0002 | c0002 | t0008 | g0006 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02886 | hp1 | a0002 | c0002 | t0007 | g0002 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02886 | hp2 | a0002 | c0003 | t0006 | g0037 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02895 | hp1 | a0002 | c0003 | t0006 | g0172 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02895 | hp2 | a0002 | c0006 | t0002 | g0235 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02896 | hp1 | a0002 | c0003 | t0006 | g0231 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02897 | hp1 | a0002 | c0003 | t0006 | g0232 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02897 | hp2 | a0002 | c0006 | t0002 | g0234 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02976 | hp1 | a0002 | c0002 | t0008 | g0171 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0089 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0190 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03017 | hp2 | a0003 | c0007 | t0001 | g0019 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03041 | hp1 | a0002 | c0002 | t0013 | g0227 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03098 | hp1 | a0002 | c0003 | t0006 | g0004 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03098 | hp2 | a0002 | c0005 | t0012 | g0032 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03130 | hp1 | a0002 | c0002 | t0010 | g0013 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03139 | hp1 | a0002 | c0002 | t0007 | g0002 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03139 | hp2 | a0002 | c0002 | t0010 | g0059 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03195 | hp1 | a0002 | c0002 | t0007 | g0002 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03209 | hp1 | a0002 | c0002 | t0010 | g0013 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03209 | hp2 | a0002 | c0002 | t0008 | g0006 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03225 | hp1 | a0002 | c0011 | t0006 | g0053 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03453 | hp1 | a0002 | c0003 | t0006 | g0004 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03453 | hp2 | a0002 | c0002 | t0021 | g0220 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03486 | hp2 | a0002 | c0002 | t0007 | g0198 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03490 | hp2 | a0003 | c0007 | t0001 | g0129 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03516 | hp1 | a0002 | c0002 | t0005 | g0062 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | ESN | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03540 | hp1 | a0002 | c0005 | t0012 | g0240 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03540 | hp2 | a0002 | c0002 | t0008 | g0006 | AFR | GWD | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03579 | hp1 | a0002 | c0002 | t0007 | g0043 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03579 | hp2 | a0002 | c0002 | t0012 | g0046 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03654 | hp1 | a0001 | c0001 | t0018 | g0158 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0210 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0026 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0026 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0116 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04228 | hp1 | a0001 | c0004 | t0005 | g0029 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | YRI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | YRI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18906 | hp1 | a0002 | c0002 | t0019 | g0173 | AFR | YRI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18944 | hp1 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18947 | hp1 | a0001 | c0001 | t0016 | g0156 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18947 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18968 | hp2 | a0001 | c0001 | t0016 | g0228 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18997 | hp1 | a0001 | c0016 | t0003 | g0195 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19030 | hp1 | a0002 | c0005 | t0027 | g0233 | AFR | LWK | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19043 | hp1 | a0002 | c0002 | t0010 | g0058 | AFR | LWK | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | LWK | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19059 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19079 | hp2 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19240 | hp1 | a0002 | c0002 | t0031 | g0060 | AFR | YRI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA19240 | hp2 | a0002 | c0002 | t0020 | g0175 | AFR | YRI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ASW | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | ASW | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20752 | hp1 | a0003 | c0007 | t0001 | g0019 | EUR | TSI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0203 | SAS | GIH | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02109 | hp1 | a0002 | c0005 | t0006 | g0239 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02109 | hp2 | a0001 | c0001 | t0024 | g0218 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0169 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02559 | hp1 | a0002 | c0002 | t0013 | g0226 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG02559 | hp2 | a0002 | c0003 | t0006 | g0004 | AFR | ACB | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03471 | hp1 | a0002 | c0002 | t0008 | g0006 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | USA | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA20300 | hp2 | a0002 | c0005 | t0006 | g0238 | AFR | USA | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA21309 | hp1 | a0001 | c0012 | t0026 | g0223 | AFR | LWK | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0150 | REF | REF | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0188 | REF | REF | TBC1D30_chr12_64819647_64886033 | TBC1D30 | chr12 | 64819647 | 64886033 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64824946 | G | C | 1 | a0004 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.67G>C | p.Gly23Arg | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/12 | 300/7764 | 67/2286 | 23/761 | chr12 | 64824946 | |||
| chr12:64875250 | C | T | 2 | a0003 a0005 |
4 | HG02818.hp1 HG03017.hp2 HG03490.hp2 others(1): Show |
missense_variant | MODERATE | c.1748C>T | p.Pro583Leu | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1981/7764 | 1748/2286 | 583/761 | chr12 | 64875250 | |||
| chr12:64875267 | G | A | 2 | a0002 a0005 |
77 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(74): Show |
missense_variant | MODERATE | c.1765G>A | p.Val589Ile | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1998/7764 | 1765/2286 | 589/761 | chr12 | 64875267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64830394 | A | G | 1 | a0001c0004 | 7 | HG00735.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
synonymous_variant | LOW | c.300A>G | p.Ala100Ala | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/12 | 533/7764 | 300/2286 | 100/761 | chr12 | 64830394 | |||
| chr12:64830472 | T | C | 4 | a0002c0005 a0002c0006 a0002c0010 others(1): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
synonymous_variant | LOW | c.378T>C | p.Asp126Asp | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/12 | 611/7764 | 378/2286 | 126/761 | chr12 | 64830472 | |||
| chr12:64832208 | C | T | 1 | a0001c0017 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.498C>T | p.Ala166Ala | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/12 | 731/7764 | 498/2286 | 166/761 | chr12 | 64832208 | |||
| chr12:64832223 | T | C | 1 | a0002c0011 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.513T>C | p.Thr171Thr | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/12 | 746/7764 | 513/2286 | 171/761 | chr12 | 64832223 | |||
| chr12:64832299 | C | T | 1 | a0001c0016 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.589C>T | p.Leu197Leu | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/12 | 822/7764 | 589/2286 | 197/761 | chr12 | 64832299 | |||
| chr12:64838825 | G | A | 1 | a0001c0012 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.906G>A | p.Ser302Ser | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/12 | 1139/7764 | 906/2286 | 302/761 | chr12 | 64838825 | |||
| chr12:64864721 | A | G | 1 | a0001c0015 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1092A>G | p.Glu364Glu | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/12 | 1325/7764 | 1092/2286 | 364/761 | chr12 | 64864721 | |||
| chr12:64866824 | C | G | 1 | a0001c0014 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1212C>G | p.Val404Val | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/12 | 1445/7764 | 1212/2286 | 404/761 | chr12 | 64866824 | |||
| chr12:64870669 | C | A | 1 | a0001c0013 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.1359C>A | p.Ser453Ser | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/12 | 1592/7764 | 1359/2286 | 453/761 | chr12 | 64870669 | |||
| chr12:64875074 | A | G | 4 | a0002c0003 a0002c0005 a0002c0010 others(1): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
synonymous_variant | LOW | c.1572A>G | p.Gly524Gly | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1805/7764 | 1572/2286 | 524/761 | chr12 | 64875074 | |||
| chr12:64875407 | G | C | 1 | a0002c0010 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1905G>C | p.Gly635Gly | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 2138/7764 | 1905/2286 | 635/761 | chr12 | 64875407 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64824771 | C | T | 1 | a0002c0002t0031 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-109C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/12 | 109 | chr12 | 64824771 | ||||||
| chr12:64824812 | C | G | 1 | a0001c0001t0015 | 3 | NA18944.hp1 NA18947.hp2 NA19079.hp2 |
5_prime_UTR_variant | MODIFIER | c.-68C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/12 | 68 | chr12 | 64824812 | ||||||
| chr12:64824847 | C | T | 1 | a0002c0002t0030 | 1 | HG02451.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/12 | chr12 | 64824847 | |||||||
| chr12:64875917 | A | T | 1 | a0005c0009t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*129A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 129 | chr12 | 64875917 | ||||||
| chr12:64876098 | G | A | 2 | a0001c0001t0004 a0001c0001t0011 |
24 | HG01081.hp2 HG01175.hp2 HG01361.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*310G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 310 | chr12 | 64876098 | ||||||
| chr12:64876155 | C | T | 1 | a0002c0002t0010 | 5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*367C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 367 | chr12 | 64876155 | ||||||
| chr12:64876240 | G | A | 1 | a0001c0001t0011 | 4 | HG02602.hp2 HG03017.hp1 HG03834.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*452G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 452 | chr12 | 64876240 | ||||||
| chr12:64876370 | A | G | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(4): Show |
61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*582A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 582 | chr12 | 64876370 | ||||||
| chr12:64876436 | A | G | 3 | a0001c0001t0014 a0001c0001t0017 a0001c0017t0017 |
5 | HG00738.hp2 HG01070.hp1 HG01106.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*648A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 648 | chr12 | 64876436 | ||||||
| chr12:64876478 | G | A | 1 | a0001c0001t0018 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 690 | chr12 | 64876478 | ||||||
| chr12:64876498 | C | T | 1 | a0002c0005t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*710C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 710 | chr12 | 64876498 | ||||||
| chr12:64876501 | C | T | 6 | a0002c0002t0006 a0002c0003t0006 a0002c0005t0006 others(3): Show |
16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*713C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 713 | chr12 | 64876501 | ||||||
| chr12:64876620 | C | A | 1 | a0002c0002t0019 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 832 | chr12 | 64876620 | ||||||
| chr12:64876629 | C | T | 2 | a0001c0012t0026 a0002c0002t0025 |
2 | HG02615.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 841 | chr12 | 64876629 | ||||||
| chr12:64876656 | A | G | 18 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0014 others(15): Show |
134 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*868A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 868 | chr12 | 64876656 | ||||||
| chr12:64876868 | C | T | 1 | a0002c0002t0008 | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1080C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1080 | chr12 | 64876868 | ||||||
| chr12:64877287 | C | T | 1 | a0001c0012t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1499C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1499 | chr12 | 64877287 | ||||||
| chr12:64877302 | G | A | 2 | a0002c0002t0010 a0002c0002t0020 |
6 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1514G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1514 | chr12 | 64877302 | ||||||
| chr12:64877362 | C | T | 1 | a0001c0001t0024 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1574C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1574 | chr12 | 64877362 | ||||||
| chr12:64877632 | G | A | 1 | a0002c0002t0021 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1844G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 1844 | chr12 | 64877632 | ||||||
| chr12:64877919 | G | T | 1 | a0002c0002t0028 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2131G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 2131 | chr12 | 64877919 | ||||||
| chr12:64877984 | G | A | 3 | a0002c0002t0007 a0002c0002t0030 a0005c0009t0029 |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2196G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 2196 | chr12 | 64877984 | ||||||
| chr12:64878439 | G | A | 2 | a0002c0002t0013 a0002c0002t0019 |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2651G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 2651 | chr12 | 64878439 | ||||||
| chr12:64878829 | C | G | 1 | a0001c0001t0023 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3041C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3041 | chr12 | 64878829 | ||||||
| chr12:64878922 | A | G | 6 | a0002c0002t0006 a0002c0003t0006 a0002c0005t0006 others(3): Show |
16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3134A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3134 | chr12 | 64878922 | ||||||
| chr12:64879013 | C | T | 1 | a0002c0002t0020 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3225C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3225 | chr12 | 64879013 | ||||||
| chr12:64879126 | A | G | 1 | a0001c0001t0014 | 3 | HG00738.hp2 HG01070.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3338A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3338 | chr12 | 64879126 | ||||||
| chr12:64879148 | A | G | 4 | a0001c0001t0005 a0001c0004t0005 a0001c0015t0005 others(1): Show |
18 | HG00423.hp1 HG00558.hp2 HG00735.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3360A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3360 | chr12 | 64879148 | ||||||
| chr12:64879256 | C | T | 15 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0015 others(12): Show |
126 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*3468C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3468 | chr12 | 64879256 | ||||||
| chr12:64879671 | T | C | 7 | a0001c0001t0005 a0001c0004t0005 a0001c0015t0005 others(4): Show |
23 | HG00423.hp1 HG00558.hp2 HG00735.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3883T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 3883 | chr12 | 64879671 | ||||||
| chr12:64879844 | G | GTATCCTG others(1): Show |
6 | a0002c0002t0006 a0002c0003t0006 a0002c0005t0006 others(3): Show |
16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4057_*4064dupTATC others(4): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4065 | INFO_REALIGN_3_PRIME | chr12 | 64879844 | |||||
| chr12:64880056 | C | T | 2 | a0002c0002t0013 a0002c0002t0019 |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4268C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4268 | chr12 | 64880056 | ||||||
| chr12:64880082 | G | A | 2 | a0002c0002t0007 a0002c0002t0030 |
11 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4294G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4294 | chr12 | 64880082 | ||||||
| chr12:64880291 | C | T | 2 | a0002c0002t0012 a0002c0005t0012 |
4 | HG02630.hp1 HG03098.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4503C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4503 | chr12 | 64880291 | ||||||
| chr12:64880412 | G | A | 3 | a0002c0002t0013 a0002c0002t0019 a0002c0002t0021 |
5 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4624G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4624 | chr12 | 64880412 | ||||||
| chr12:64880421 | C | A | 1 | a0001c0001t0016 | 2 | NA18947.hp1 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4633C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4633 | chr12 | 64880421 | ||||||
| chr12:64880445 | T | C | 2 | a0002c0002t0010 a0002c0002t0020 |
6 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4657T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 12/12 | 4657 | chr12 | 64880445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64825248 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0005g0033 |
3 | HG01168.hp1 HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.154+215G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64825248 | |||||||
| chr12:64825275 | C | G | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+242C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64825275 | |||||||
| chr12:64825519 | G | T | 1 | a0001c0001t0001g0031 | 2 | NA18944.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.154+486G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64825519 | |||||||
| chr12:64825598 | G | C | 1 | a0001c0001t0005g0036 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154+565G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64825598 | |||||||
| chr12:64826063 | T | C | 12 | a0001c0001t0001g0042 a0002c0002t0001g0039 a0002c0002t0007g0002 others(9): Show |
19 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.154+1030T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826063 | |||||||
| chr12:64826089 | C | T | 2 | a0002c0003t0006g0231 a0002c0003t0006g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.154+1056C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826089 | |||||||
| chr12:64826180 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154+1147A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826180 | |||||||
| chr12:64826227 | G | T | 1 | a0001c0001t0016g0228 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.154+1194G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826227 | |||||||
| chr12:64826296 | G | A | 1 | a0001c0014t0001g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.154+1263G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826296 | |||||||
| chr12:64826322 | G | T | 2 | a0002c0002t0013g0226 a0002c0002t0013g0227 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154+1289G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826322 | |||||||
| chr12:64826496 | C | A | 4 | a0001c0001t0001g0048 a0001c0001t0003g0011 a0001c0001t0003g0049 others(1): Show |
5 | HG00621.hp1 NA18948.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-1339C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826496 | |||||||
| chr12:64826514 | C | G | 2 | a0001c0001t0003g0224 a0001c0001t0003g0225 |
2 | HG01081.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.155-1321C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826514 | |||||||
| chr12:64826587 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(159): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.155-1248G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826587 | |||||||
| chr12:64826630 | C | T | 1 | a0001c0012t0026g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-1205C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826630 | |||||||
| chr12:64826849 | A | T | 2 | a0002c0003t0006g0231 a0002c0003t0006g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.155-986A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826849 | |||||||
| chr12:64826902 | C | T | 2 | a0002c0002t0013g0226 a0002c0002t0013g0227 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.155-933C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826902 | |||||||
| chr12:64826918 | T | A | 3 | a0002c0002t0008g0170 a0002c0002t0008g0171 a0002c0003t0006g0172 |
3 | HG02809.hp2 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.155-917T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826918 | |||||||
| chr12:64826932 | G | C | 1 | a0001c0001t0003g0051 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.155-903G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64826932 | |||||||
| chr12:64827034 | A | T | 3 | a0002c0002t0002g0023 a0002c0002t0002g0168 a0002c0002t0002g0169 |
4 | HG02145.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-801A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827034 | |||||||
| chr12:64827076 | G | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00741.hp2 HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.155-759G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827076 | |||||||
| chr12:64827169 | G | A | 1 | a0002c0005t0027g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-666G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827169 | |||||||
| chr12:64827170 | C | A | 1 | a0002c0005t0027g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-665C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827170 | |||||||
| chr12:64827183 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.155-652C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827183 | |||||||
| chr12:64827262 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.155-573C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827262 | |||||||
| chr12:64827303 | G | T | 1 | a0004c0008t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.155-532G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827303 | |||||||
| chr12:64827531 | T | C | 1 | a0002c0002t0008g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.155-304T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827531 | |||||||
| chr12:64827649 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.155-186G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827649 | |||||||
| chr12:64827823 | T | A | 1 | a0001c0001t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.155-12T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 1/11 | chr12 | 64827823 | |||||||
| chr12:64827990 | T | G | 1 | a0001c0004t0005g0024 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.216+94T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 2/11 | chr12 | 64827990 | |||||||
| chr12:64828175 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.217-269A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 2/11 | chr12 | 64828175 | |||||||
| chr12:64828520 | C | G | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+11C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64828520 | |||||||
| chr12:64828567 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.282+58C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64828567 | |||||||
| chr12:64828874 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(28): Show |
36 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.282+365C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64828874 | |||||||
| chr12:64828894 | G | A | 1 | a0002c0011t0006g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282+385G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64828894 | |||||||
| chr12:64829088 | G | A | 2 | a0002c0002t0002g0174 a0002c0002t0019g0173 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.282+579G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829088 | |||||||
| chr12:64829110 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+601G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829110 | |||||||
| chr12:64829262 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18944.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.282+753G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829262 | |||||||
| chr12:64829316 | C | G | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+807C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829316 | |||||||
| chr12:64829328 | A | G | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.282+819A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829328 | |||||||
| chr12:64829346 | A | G | 8 | a0001c0001t0024g0218 a0002c0002t0001g0217 a0002c0002t0002g0030 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.282+837A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829346 | |||||||
| chr12:64829388 | C | T | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+879C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829388 | |||||||
| chr12:64829464 | G | C | 1 | a0002c0002t0031g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283-913G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829464 | |||||||
| chr12:64829469 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283-908C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829469 | |||||||
| chr12:64829527 | G | A | 1 | a0002c0011t0006g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.283-850G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829527 | |||||||
| chr12:64829632 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.283-745G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829632 | |||||||
| chr12:64829682 | T | C | 2 | a0002c0002t0001g0217 a0002c0002t0002g0030 |
3 | HG02922.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.283-695T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829682 | |||||||
| chr12:64829871 | A | C | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-506A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64829871 | |||||||
| chr12:64830296 | C | T | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.283-81C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 3/11 | chr12 | 64830296 | |||||||
| chr12:64830772 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+270G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64830772 | |||||||
| chr12:64830818 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.408+316C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64830818 | |||||||
| chr12:64830931 | C | T | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+429C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64830931 | |||||||
| chr12:64831105 | A | C | 1 | a0001c0001t0011g0216 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.408+603A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831105 | |||||||
| chr12:64831126 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408+624A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831126 | |||||||
| chr12:64831273 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
8 | NA18945.hp2 NA18956.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+771G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831273 | |||||||
| chr12:64831459 | T | TA | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-660_409-659ins others(1): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831459 | |||||||
| chr12:64831679 | C | G | 1 | a0002c0005t0027g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.409-440C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831679 | |||||||
| chr12:64831749 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.409-370A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831749 | |||||||
| chr12:64831791 | T | C | 2 | a0002c0006t0002g0234 a0002c0006t0002g0235 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.409-328T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831791 | |||||||
| chr12:64831825 | C | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.409-294C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64831825 | |||||||
| chr12:64832020 | C | T | 3 | a0002c0002t0008g0006 a0002c0002t0008g0052 a0002c0002t0025g0136 |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-99C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64832020 | |||||||
| chr12:64832029 | G | T | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-90G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 4/11 | chr12 | 64832029 | |||||||
| chr12:64832367 | A | C | 3 | a0002c0005t0012g0032 a0002c0005t0012g0240 a0005c0009t0029g0241 |
4 | HG02630.hp1 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+63A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64832367 | |||||||
| chr12:64832370 | T | C | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.594+66T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64832370 | |||||||
| chr12:64832435 | G | A | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.594+131G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64832435 | |||||||
| chr12:64832534 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.594+230T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64832534 | |||||||
| chr12:64832721 | A | G | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.594+417A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64832721 | |||||||
| chr12:64832814 | G | A | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.594+510G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64832814 | |||||||
| chr12:64833097 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.594+793G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64833097 | |||||||
| chr12:64833274 | T | C | 1 | a0002c0002t0031g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.594+970T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64833274 | |||||||
| chr12:64833292 | A | G | 1 | a0002c0002t0002g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+988A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64833292 | |||||||
| chr12:64833624 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.594+1320A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64833624 | |||||||
| chr12:64833655 | G | A | 1 | a0002c0002t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.594+1351G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64833655 | |||||||
| chr12:64833814 | G | T | 1 | a0001c0001t0003g0049 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.594+1510G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64833814 | |||||||
| chr12:64833817 | G | GT | 10 | a0001c0001t0024g0218 a0002c0002t0001g0217 a0002c0002t0002g0030 others(7): Show |
11 | HG01891.hp2 HG02109.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.594+1519dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 64833817 | ||||||
| chr12:64833867 | G | GT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(187): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.594+1573dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 64833867 | ||||||
| chr12:64834046 | G | T | 3 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0002c0003t0006g0176 |
3 | HG01081.hp1 HG02055.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.594+1742G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834046 | |||||||
| chr12:64834404 | C | CT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(43): Show |
58 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.595-2066dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 64834404 | ||||||
| chr12:64834404 | CT | C | 7 | a0001c0001t0001g0063 a0001c0001t0004g0180 a0001c0001t0005g0178 others(4): Show |
7 | HG00558.hp2 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-2066delT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 64834404 | ||||||
| chr12:64834466 | G | A | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.595-2024G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834466 | |||||||
| chr12:64834477 | T | G | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.595-2013T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834477 | |||||||
| chr12:64834562 | A | G | 2 | a0002c0002t0013g0226 a0002c0002t0013g0227 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.595-1928A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834562 | |||||||
| chr12:64834612 | G | T | 3 | a0002c0002t0008g0006 a0002c0002t0008g0052 a0002c0002t0025g0136 |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-1878G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834612 | |||||||
| chr12:64834688 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.595-1802C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834688 | |||||||
| chr12:64834698 | C | T | 2 | a0002c0002t0013g0226 a0002c0002t0013g0227 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.595-1792C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834698 | |||||||
| chr12:64834707 | C | CT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(79): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.595-1759dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 64834707 | ||||||
| chr12:64834707 | C | CTT | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG00597.hp1 HG02486.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-1760_595-1759d others(4): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | 64834707 | ||||||
| chr12:64834773 | G | A | 8 | a0001c0001t0024g0218 a0002c0002t0001g0217 a0002c0002t0002g0030 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.595-1717G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834773 | |||||||
| chr12:64834827 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.595-1663A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64834827 | |||||||
| chr12:64835309 | A | T | 1 | a0002c0011t0006g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.595-1181A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835309 | |||||||
| chr12:64835461 | C | T | 2 | a0002c0003t0006g0231 a0002c0003t0006g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.595-1029C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835461 | |||||||
| chr12:64835463 | A | G | 1 | a0002c0002t0031g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.595-1027A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835463 | |||||||
| chr12:64835481 | A | G | 3 | a0002c0002t0008g0006 a0002c0002t0008g0052 a0002c0002t0025g0136 |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-1009A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835481 | |||||||
| chr12:64835565 | G | A | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-925G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835565 | |||||||
| chr12:64835620 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.595-870G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835620 | |||||||
| chr12:64835647 | A | C | 2 | a0002c0003t0006g0231 a0002c0003t0006g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.595-843A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835647 | |||||||
| chr12:64835663 | C | G | 1 | a0001c0004t0005g0029 | 2 | HG01074.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.595-827C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835663 | |||||||
| chr12:64835715 | A | G | 1 | a0001c0001t0004g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.595-775A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835715 | |||||||
| chr12:64835819 | G | T | 1 | a0001c0004t0005g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.595-671G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835819 | |||||||
| chr12:64835908 | A | G | 2 | a0001c0001t0003g0107 a0001c0001t0003g0113 |
2 | HG00597.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.595-582A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835908 | |||||||
| chr12:64835934 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0003g0011 a0001c0001t0003g0049 others(1): Show |
5 | HG00621.hp1 NA18948.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-556A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64835934 | |||||||
| chr12:64836104 | G | T | 1 | a0001c0001t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.595-386G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64836104 | |||||||
| chr12:64836326 | G | A | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-164G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 5/11 | chr12 | 64836326 | |||||||
| chr12:64836839 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.763+181A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64836839 | |||||||
| chr12:64836860 | AG | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0075 others(3): Show |
6 | HG00738.hp1 HG01106.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.763+204delG | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 64836860 | ||||||
| chr12:64837162 | C | T | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.763+504C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837162 | |||||||
| chr12:64837241 | C | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.763+583C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837241 | |||||||
| chr12:64837327 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.763+669T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837327 | |||||||
| chr12:64837451 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.763+793G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837451 | |||||||
| chr12:64837534 | A | G | 8 | a0001c0001t0001g0042 a0002c0002t0001g0039 a0002c0002t0007g0002 others(5): Show |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.763+876A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837534 | |||||||
| chr12:64837798 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.764-885C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837798 | |||||||
| chr12:64837893 | A | G | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.764-790A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64837893 | |||||||
| chr12:64838119 | C | T | 3 | a0002c0002t0008g0006 a0002c0002t0008g0052 a0002c0002t0025g0136 |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-564C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64838119 | |||||||
| chr12:64838215 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.764-468T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64838215 | |||||||
| chr12:64838404 | C | A | 8 | a0001c0001t0024g0218 a0002c0002t0001g0217 a0002c0002t0002g0030 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.764-279C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64838404 | |||||||
| chr12:64838478 | A | C | 1 | a0001c0004t0005g0029 | 2 | HG01074.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.764-205A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 6/11 | chr12 | 64838478 | |||||||
| chr12:64838875 | C | G | 1 | a0001c0001t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.932+24C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64838875 | |||||||
| chr12:64838919 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(29): Show |
42 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.932+68C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64838919 | |||||||
| chr12:64839040 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.932+189T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839040 | |||||||
| chr12:64839270 | A | G | 8 | a0001c0001t0024g0218 a0002c0002t0001g0217 a0002c0002t0002g0030 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.932+419A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839270 | |||||||
| chr12:64839612 | G | C | 1 | a0002c0002t0001g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.932+761G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839612 | |||||||
| chr12:64839722 | A | C | 1 | a0001c0001t0003g0105 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.932+871A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839722 | |||||||
| chr12:64839865 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0003g0011 a0001c0001t0003g0049 others(1): Show |
5 | HG00621.hp1 NA18948.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.932+1014C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839865 | |||||||
| chr12:64839866 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18944.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.932+1015G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839866 | |||||||
| chr12:64839869 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.932+1018G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839869 | |||||||
| chr12:64839932 | G | A | 1 | a0001c0001t0017g0181 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.932+1081G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64839932 | |||||||
| chr12:64840004 | C | CA | 15 | a0001c0001t0002g0007 a0001c0001t0002g0183 a0001c0001t0002g0184 others(12): Show |
18 | HG00140.hp2 HG00621.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.932+1177dupA | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAA | 17 | a0001c0001t0001g0042 a0001c0001t0024g0218 a0002c0002t0001g0039 others(14): Show |
25 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.932+1175_932+1177d others(5): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(3): Show |
1 | a0002c0011t0006g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.932+1168_932+1177d others(12): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(6): Show |
3 | a0002c0002t0008g0170 a0002c0002t0008g0171 a0002c0003t0006g0172 |
3 | HG02809.hp2 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.932+1165_932+1177d others(15): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.932+1164_932+1177d others(16): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0003g0225 a0002c0003t0006g0176 |
2 | HG02055.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.932+1163_932+1177d others(17): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(9): Show |
1 | a0002c0005t0027g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.932+1162_932+1177d others(18): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(11): Show |
1 | a0002c0002t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.932+1160_932+1177d others(20): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(12): Show |
4 | a0002c0002t0013g0226 a0002c0006t0002g0234 a0002c0006t0002g0235 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.932+1159_932+1177d others(21): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(13): Show |
3 | a0002c0005t0006g0239 a0002c0005t0012g0032 a0002c0005t0012g0240 |
4 | HG02109.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.932+1158_932+1177d others(22): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(14): Show |
3 | a0002c0002t0020g0175 a0002c0005t0006g0238 a0002c0010t0006g0236 |
3 | HG02723.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.932+1157_932+1177d others(23): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(15): Show |
1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.932+1156_932+1177d others(24): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | C | CAAAAAAA others(16): Show |
1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.932+1155_932+1177d others(25): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | CAAAA | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0079 others(11): Show |
15 | HG00741.hp1 HG00741.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.932+1174_932+1177d others(6): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840004 | CAAAAA | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.932+1173_932+1177d others(7): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840004 | ||||||
| chr12:64840027 | A | AAAAAAAA others(19): Show |
2 | a0002c0002t0010g0013 a0002c0002t0010g0057 |
3 | HG02622.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.932+1177_932+1178i others(28): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840027 | ||||||
| chr12:64840027 | A | AAAAAAAA others(18): Show |
1 | a0002c0002t0010g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.932+1177_932+1178i others(27): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 64840027 | ||||||
| chr12:64840027 | A | C | 1 | a0002c0002t0010g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.932+1176A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840027 | |||||||
| chr12:64840057 | A | C | 6 | a0002c0005t0012g0032 a0002c0005t0012g0240 a0002c0006t0002g0234 others(3): Show |
7 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.932+1206A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840057 | |||||||
| chr12:64840202 | T | C | 6 | a0002c0002t0002g0023 a0002c0002t0002g0080 a0002c0002t0002g0081 others(3): Show |
7 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.932+1351T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840202 | |||||||
| chr12:64840548 | T | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(176): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.932+1697T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840548 | |||||||
| chr12:64840768 | T | A | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.932+1917T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840768 | |||||||
| chr12:64840911 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.932+2060A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840911 | |||||||
| chr12:64840966 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.932+2115C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64840966 | |||||||
| chr12:64841214 | C | T | 3 | a0001c0001t0003g0185 a0001c0001t0017g0181 a0001c0017t0017g0209 |
3 | HG01106.hp2 HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.933-2166C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64841214 | |||||||
| chr12:64841279 | C | T | 1 | a0001c0014t0001g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.933-2101C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64841279 | |||||||
| chr12:64841620 | G | T | 1 | a0001c0004t0001g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.933-1760G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64841620 | |||||||
| chr12:64841641 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.933-1739G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64841641 | |||||||
| chr12:64841652 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.933-1728G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64841652 | |||||||
| chr12:64841724 | T | C | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.933-1656T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64841724 | |||||||
| chr12:64842120 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.933-1260G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842120 | |||||||
| chr12:64842220 | G | T | 1 | a0001c0001t0003g0104 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.933-1160G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842220 | |||||||
| chr12:64842239 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.933-1141A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842239 | |||||||
| chr12:64842252 | G | A | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.933-1128G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842252 | |||||||
| chr12:64842504 | T | G | 1 | a0002c0011t0006g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.933-876T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842504 | |||||||
| chr12:64842534 | G | A | 1 | a0001c0004t0005g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.933-846G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842534 | |||||||
| chr12:64842857 | G | A | 1 | a0001c0001t0005g0213 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.933-523G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842857 | |||||||
| chr12:64842888 | C | T | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.933-492C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64842888 | |||||||
| chr12:64843109 | G | A | 2 | a0003c0007t0001g0019 a0003c0007t0001g0129 |
3 | HG03017.hp2 HG03490.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.933-271G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64843109 | |||||||
| chr12:64843201 | G | T | 1 | a0004c0008t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.933-179G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64843201 | |||||||
| chr12:64843232 | C | G | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.933-148C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64843232 | |||||||
| chr12:64843253 | C | G | 1 | a0001c0001t0009g0055 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.933-127C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 7/11 | chr12 | 64843253 | |||||||
| chr12:64843507 | G | A | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1038+22G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64843507 | |||||||
| chr12:64843515 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1038+30C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64843515 | |||||||
| chr12:64843516 | G | A | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+31G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64843516 | |||||||
| chr12:64843559 | G | A | 1 | a0002c0011t0006g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1038+74G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64843559 | |||||||
| chr12:64843613 | A | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0108 a0002c0002t0001g0039 others(11): Show |
21 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1038+128A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64843613 | |||||||
| chr12:64843859 | G | A | 5 | a0001c0001t0024g0218 a0002c0002t0001g0217 a0002c0002t0002g0030 others(2): Show |
6 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+374G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64843859 | |||||||
| chr12:64844012 | T | C | 10 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1038+527T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844012 | |||||||
| chr12:64844045 | C | T | 7 | a0001c0001t0009g0012 a0001c0001t0009g0055 a0001c0001t0009g0056 others(4): Show |
8 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+560C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844045 | |||||||
| chr12:64844122 | T | C | 1 | a0002c0005t0012g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1038+637T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844122 | |||||||
| chr12:64844217 | A | G | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+732A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844217 | |||||||
| chr12:64844283 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1038+798C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844283 | |||||||
| chr12:64844306 | CTT | C | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+823_1038+824d others(4): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64844306 | ||||||
| chr12:64844385 | C | T | 11 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0012g0032 others(8): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+900C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844385 | |||||||
| chr12:64844750 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1038+1265C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844750 | |||||||
| chr12:64844753 | TTAAGTGA others(87): Show |
T | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1038+1299_1038+139 others(98): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64844753 | ||||||
| chr12:64844763 | A | G | 5 | a0002c0002t0002g0016 a0002c0002t0002g0067 a0002c0002t0002g0068 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+1278A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64844763 | |||||||
| chr12:64845012 | C | A | 3 | a0002c0006t0002g0234 a0002c0006t0002g0235 a0002c0006t0002g0237 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1038+1527C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845012 | |||||||
| chr12:64845314 | C | T | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+1829C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845314 | |||||||
| chr12:64845453 | G | A | 2 | a0001c0001t0005g0036 a0002c0002t0007g0044 |
2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1038+1968G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845453 | |||||||
| chr12:64845455 | G | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0116 a0002c0002t0002g0215 |
4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+1970G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845455 | |||||||
| chr12:64845459 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1038+1974G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845459 | |||||||
| chr12:64845460 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1038+1975C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845460 | |||||||
| chr12:64845461 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1038+1976T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845461 | |||||||
| chr12:64845474 | C | T | 1 | a0002c0010t0006g0236 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1038+1989C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845474 | |||||||
| chr12:64845522 | C | T | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+2037C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845522 | |||||||
| chr12:64845681 | G | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(25): Show |
33 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1038+2196G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845681 | |||||||
| chr12:64845690 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1038+2205T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845690 | |||||||
| chr12:64845726 | CA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1038+2259delA | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64845726 | ||||||
| chr12:64845726 | CAA | C | 11 | a0001c0001t0005g0028 a0001c0001t0005g0036 a0001c0001t0005g0178 others(8): Show |
14 | HG00423.hp1 HG00558.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038+2258_1038+225 others(6): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64845726 | ||||||
| chr12:64845816 | T | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+2331T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845816 | |||||||
| chr12:64845873 | T | A | 8 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+2388T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845873 | |||||||
| chr12:64845906 | C | T | 6 | a0001c0001t0001g0110 a0001c0001t0003g0066 a0001c0001t0003g0077 others(3): Show |
6 | HG02056.hp1 HG02083.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+2421C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64845906 | |||||||
| chr12:64846247 | A | G | 1 | a0001c0001t0023g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1038+2762A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846247 | |||||||
| chr12:64846282 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1038+2797A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846282 | |||||||
| chr12:64846434 | T | C | 6 | a0001c0001t0005g0178 a0001c0001t0005g0201 a0001c0004t0005g0024 others(3): Show |
8 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1038+2949T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846434 | |||||||
| chr12:64846512 | A | G | 9 | a0002c0002t0002g0023 a0002c0002t0002g0080 a0002c0002t0002g0081 others(6): Show |
10 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1038+3027A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846512 | |||||||
| chr12:64846669 | G | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+3184G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846669 | |||||||
| chr12:64846682 | T | C | 1 | a0002c0002t0007g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1038+3197T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846682 | |||||||
| chr12:64846994 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1038+3509C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64846994 | |||||||
| chr12:64847334 | A | G | 1 | a0002c0002t0010g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+3849A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847334 | |||||||
| chr12:64847358 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1038+3873T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847358 | |||||||
| chr12:64847592 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1038+4107A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847592 | |||||||
| chr12:64847895 | A | G | 4 | a0002c0002t0005g0062 a0002c0002t0013g0103 a0002c0002t0013g0226 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4410A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847895 | |||||||
| chr12:64847958 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1038+4473T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847958 | |||||||
| chr12:64847969 | G | A | 22 | a0001c0001t0003g0212 a0001c0001t0004g0008 a0001c0001t0004g0072 others(19): Show |
26 | HG01099.hp2 HG01175.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1038+4484G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847969 | |||||||
| chr12:64847996 | G | A | 1 | a0002c0002t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1038+4511G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64847996 | |||||||
| chr12:64848022 | C | G | 21 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0005g0062 others(18): Show |
26 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1038+4537C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848022 | |||||||
| chr12:64848209 | C | T | 2 | a0001c0001t0004g0196 a0001c0016t0003g0195 |
2 | NA18953.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1038+4724C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848209 | |||||||
| chr12:64848288 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+4803A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848288 | |||||||
| chr12:64848297 | T | C | 6 | a0002c0002t0006g0089 a0002c0002t0008g0006 a0002c0002t0008g0052 others(3): Show |
9 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+4812T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848297 | |||||||
| chr12:64848481 | G | A | 1 | a0002c0006t0002g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1038+4996G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848481 | |||||||
| chr12:64848836 | T | G | 3 | a0001c0001t0001g0147 a0001c0001t0003g0154 a0001c0001t0016g0156 |
3 | HG02074.hp1 NA18947.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1038+5351T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848836 | |||||||
| chr12:64848937 | T | A | 1 | a0001c0001t0004g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1038+5452T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848937 | |||||||
| chr12:64848962 | C | A | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1038+5477C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64848962 | |||||||
| chr12:64849066 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+5581G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64849066 | |||||||
| chr12:64849618 | T | C | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1038+6133T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64849618 | |||||||
| chr12:64849698 | G | A | 14 | a0002c0002t0002g0023 a0002c0002t0002g0030 a0002c0002t0002g0067 others(11): Show |
16 | HG01361.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1038+6213G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64849698 | |||||||
| chr12:64849739 | G | A | 2 | a0002c0002t0013g0103 a0002c0002t0013g0226 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1038+6254G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64849739 | |||||||
| chr12:64849767 | G | T | 4 | a0002c0002t0005g0062 a0002c0002t0013g0103 a0002c0002t0013g0226 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+6282G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64849767 | |||||||
| chr12:64850005 | T | G | 10 | a0002c0002t0002g0023 a0002c0002t0002g0080 a0002c0002t0002g0081 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+6520T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850005 | |||||||
| chr12:64850132 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1038+6647C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850132 | |||||||
| chr12:64850266 | C | G | 4 | a0002c0002t0005g0062 a0002c0002t0013g0103 a0002c0002t0013g0226 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+6781C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850266 | |||||||
| chr12:64850334 | T | C | 57 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(54): Show |
70 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(67): Show |
intron_variant | MODIFIER | c.1038+6849T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850334 | |||||||
| chr12:64850540 | T | C | 1 | a0001c0012t0026g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1038+7055T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850540 | |||||||
| chr12:64850711 | T | C | 1 | a0002c0002t0008g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1038+7226T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850711 | |||||||
| chr12:64850748 | G | A | 1 | a0001c0004t0005g0029 | 2 | HG01074.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1038+7263G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850748 | |||||||
| chr12:64850876 | AGAATTTG others(5): Show |
A | 1 | a0001c0012t0026g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1038+7396_1038+740 others(16): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64850876 | ||||||
| chr12:64850957 | T | C | 57 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(54): Show |
70 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(67): Show |
intron_variant | MODIFIER | c.1038+7472T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64850957 | |||||||
| chr12:64851100 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0003g0084 a0001c0001t0003g0104 others(1): Show |
4 | HG01261.hp1 NA18946.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+7615C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64851100 | |||||||
| chr12:64851113 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1038+7628G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64851113 | |||||||
| chr12:64851244 | T | C | 2 | a0002c0003t0006g0231 a0002c0003t0006g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1038+7759T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64851244 | |||||||
| chr12:64851830 | G | A | 1 | a0001c0001t0004g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1038+8345G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64851830 | |||||||
| chr12:64851841 | A | G | 1 | a0001c0015t0005g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1038+8356A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64851841 | |||||||
| chr12:64851925 | C | T | 13 | a0002c0002t0002g0023 a0002c0002t0002g0030 a0002c0002t0002g0067 others(10): Show |
15 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1038+8440C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64851925 | |||||||
| chr12:64852036 | C | CT | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+8551_1038+855 others(5): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852036 | |||||||
| chr12:64852136 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0020 |
4 | NA18942.hp1 NA18961.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+8651C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852136 | |||||||
| chr12:64852247 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1038+8762C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852247 | |||||||
| chr12:64852260 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+8775G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852260 | |||||||
| chr12:64852271 | C | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+8786C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852271 | |||||||
| chr12:64852648 | A | AG | 5 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(2): Show |
6 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+9164dupG | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64852648 | ||||||
| chr12:64852703 | A | C | 6 | a0002c0002t0006g0089 a0002c0002t0008g0006 a0002c0002t0008g0052 others(3): Show |
9 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+9218A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852703 | |||||||
| chr12:64852822 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1038+9337C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852822 | |||||||
| chr12:64852866 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0108 others(1): Show |
5 | HG02717.hp1 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+9381G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64852866 | |||||||
| chr12:64853095 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1038+9610C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853095 | |||||||
| chr12:64853120 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+9635G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853120 | |||||||
| chr12:64853219 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0002g0199 |
2 | HG00673.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1038+9734C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853219 | |||||||
| chr12:64853225 | C | T | 8 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(5): Show |
9 | HG01884.hp2 HG02622.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+9740C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853225 | |||||||
| chr12:64853387 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+9902A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853387 | |||||||
| chr12:64853481 | C | T | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1038+9996C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853481 | |||||||
| chr12:64853675 | A | G | 2 | a0001c0012t0026g0223 a0002c0002t0012g0046 |
2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1038+10190A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853675 | |||||||
| chr12:64853773 | G | T | 18 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0005g0062 others(15): Show |
23 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1038+10288G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853773 | |||||||
| chr12:64853876 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+10391A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853876 | |||||||
| chr12:64853891 | C | T | 16 | a0001c0001t0004g0194 a0001c0001t0004g0211 a0002c0003t0006g0004 others(13): Show |
20 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1038+10406C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853891 | |||||||
| chr12:64853910 | G | A | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1038+10425G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853910 | |||||||
| chr12:64853911 | C | T | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+10426C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64853911 | |||||||
| chr12:64854146 | C | T | 6 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(3): Show |
9 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-10522C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854146 | |||||||
| chr12:64854167 | G | A | 1 | a0001c0001t0004g0214 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1039-10501G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854167 | |||||||
| chr12:64854289 | T | C | 6 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(3): Show |
7 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-10379T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854289 | |||||||
| chr12:64854378 | C | T | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1039-10290C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854378 | |||||||
| chr12:64854384 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1039-10284C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854384 | |||||||
| chr12:64854498 | C | CT | 38 | a0001c0001t0004g0193 a0002c0002t0001g0039 a0002c0002t0001g0217 others(35): Show |
46 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.1039-10156dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64854498 | ||||||
| chr12:64854498 | C | CTT | 16 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(13): Show |
20 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1039-10157_1039-10 others(8): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64854498 | ||||||
| chr12:64854498 | C | CTTTCTT | 13 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(10): Show |
17 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1039-10167_1039-10 others(12): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64854498 | ||||||
| chr12:64854534 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-10134A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854534 | |||||||
| chr12:64854564 | A | G | 57 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(54): Show |
70 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(67): Show |
intron_variant | MODIFIER | c.1039-10104A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854564 | |||||||
| chr12:64854581 | G | A | 9 | a0002c0002t0002g0023 a0002c0002t0002g0080 a0002c0002t0002g0081 others(6): Show |
10 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1039-10087G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854581 | |||||||
| chr12:64854687 | G | T | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-9981G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854687 | |||||||
| chr12:64854697 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0137 |
4 | HG02280.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-9971G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854697 | |||||||
| chr12:64854803 | G | A | 1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1039-9865G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854803 | |||||||
| chr12:64854968 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0002g0097 |
3 | HG00140.hp1 HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1039-9700A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854968 | |||||||
| chr12:64854976 | T | C | 1 | a0001c0013t0003g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1039-9692T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64854976 | |||||||
| chr12:64855093 | GT | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-9566delT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64855093 | ||||||
| chr12:64855292 | C | T | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-9376C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855292 | |||||||
| chr12:64855424 | T | A | 1 | a0001c0004t0005g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1039-9244T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855424 | |||||||
| chr12:64855509 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1039-9159A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855509 | |||||||
| chr12:64855631 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-9037G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855631 | |||||||
| chr12:64855719 | C | T | 8 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0007g0002 others(5): Show |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039-8949C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855719 | |||||||
| chr12:64855809 | G | A | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-8859G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855809 | |||||||
| chr12:64855835 | T | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-8833T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855835 | |||||||
| chr12:64855890 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-8778G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855890 | |||||||
| chr12:64855927 | A | G | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1039-8741A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64855927 | |||||||
| chr12:64856064 | T | A | 1 | a0002c0002t0030g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1039-8604T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856064 | |||||||
| chr12:64856067 | T | C | 2 | a0001c0001t0002g0187 a0001c0001t0002g0200 |
2 | HG00280.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1039-8601T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856067 | |||||||
| chr12:64856079 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1039-8589G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856079 | |||||||
| chr12:64856126 | A | G | 3 | a0002c0002t0013g0103 a0002c0002t0013g0226 a0002c0002t0013g0227 |
3 | HG02280.hp1 HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1039-8542A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856126 | |||||||
| chr12:64856500 | A | ACT | 9 | a0001c0012t0026g0223 a0002c0002t0006g0089 a0002c0002t0008g0006 others(6): Show |
12 | HG01361.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039-8166_1039-816 others(6): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64856500 | ||||||
| chr12:64856503 | C | CTT | 58 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(55): Show |
71 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(68): Show |
intron_variant | MODIFIER | c.1039-8165_1039-816 others(6): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856503 | |||||||
| chr12:64856569 | G | A | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1039-8099G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856569 | |||||||
| chr12:64856589 | C | T | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1039-8079C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856589 | |||||||
| chr12:64856608 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1039-8060T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856608 | |||||||
| chr12:64856762 | A | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-7906A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856762 | |||||||
| chr12:64856801 | C | T | 1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1039-7867C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856801 | |||||||
| chr12:64856853 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00438.hp2 HG02083.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1039-7815G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856853 | |||||||
| chr12:64856881 | A | C | 2 | a0001c0001t0005g0178 a0001c0001t0005g0201 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1039-7787A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856881 | |||||||
| chr12:64856963 | T | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-7705T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64856963 | |||||||
| chr12:64857001 | C | A | 1 | a0001c0012t0026g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1039-7667C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857001 | |||||||
| chr12:64857085 | T | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-7583T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857085 | |||||||
| chr12:64857404 | A | G | 43 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(40): Show |
52 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.1039-7264A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857404 | |||||||
| chr12:64857409 | C | G | 1 | a0002c0002t0007g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1039-7259C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857409 | |||||||
| chr12:64857568 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-7100G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857568 | |||||||
| chr12:64857615 | G | A | 9 | a0001c0012t0026g0223 a0002c0002t0006g0089 a0002c0002t0008g0006 others(6): Show |
12 | HG01361.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039-7053G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857615 | |||||||
| chr12:64857698 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1039-6970G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857698 | |||||||
| chr12:64857879 | C | T | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1039-6789C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64857879 | |||||||
| chr12:64858017 | C | T | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-6651C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858017 | |||||||
| chr12:64858146 | G | C | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-6522G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858146 | |||||||
| chr12:64858186 | C | T | 4 | a0002c0002t0005g0062 a0002c0002t0013g0103 a0002c0002t0013g0226 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-6482C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858186 | |||||||
| chr12:64858338 | A | G | 11 | a0001c0001t0005g0028 a0001c0001t0005g0036 a0001c0001t0005g0178 others(8): Show |
14 | HG00423.hp1 HG00558.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1039-6330A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858338 | |||||||
| chr12:64858340 | T | C | 14 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(11): Show |
16 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1039-6328T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858340 | |||||||
| chr12:64858551 | T | C | 4 | a0001c0001t0009g0012 a0001c0001t0009g0055 a0001c0001t0009g0056 others(1): Show |
5 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-6117T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858551 | |||||||
| chr12:64858663 | C | T | 1 | a0001c0001t0004g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1039-6005C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858663 | |||||||
| chr12:64858854 | C | T | 5 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0005t0027g0233 others(2): Show |
5 | HG02109.hp1 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-5814C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858854 | |||||||
| chr12:64858857 | C | T | 2 | a0001c0001t0004g0194 a0001c0001t0004g0211 |
2 | HG01175.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1039-5811C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858857 | |||||||
| chr12:64858927 | T | C | 1 | a0001c0013t0003g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1039-5741T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64858927 | |||||||
| chr12:64859020 | CTG | C | 13 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(10): Show |
17 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1039-5628_1039-562 others(6): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64859020 | ||||||
| chr12:64859075 | C | T | 8 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-5593C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859075 | |||||||
| chr12:64859236 | G | A | 1 | a0002c0002t0013g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1039-5432G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859236 | |||||||
| chr12:64859253 | G | A | 5 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(2): Show |
6 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-5415G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859253 | |||||||
| chr12:64859464 | G | A | 4 | a0002c0002t0005g0062 a0002c0002t0013g0103 a0002c0002t0013g0226 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5204G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859464 | |||||||
| chr12:64859734 | G | A | 1 | a0002c0002t0002g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1039-4934G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859734 | |||||||
| chr12:64859764 | C | CA | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-4902dupA | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64859764 | ||||||
| chr12:64859918 | C | T | 1 | a0002c0002t0002g0016 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1039-4750C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859918 | |||||||
| chr12:64859919 | G | A | 1 | a0002c0002t0025g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1039-4749G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859919 | |||||||
| chr12:64859949 | G | A | 8 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(5): Show |
9 | HG01884.hp2 HG02622.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-4719G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64859949 | |||||||
| chr12:64860017 | C | CT | 6 | a0001c0001t0003g0096 a0002c0002t0006g0089 a0002c0002t0008g0006 others(3): Show |
9 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-4633dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64860017 | ||||||
| chr12:64860017 | C | T | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-4651C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860017 | |||||||
| chr12:64860017 | CT | C | 19 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0110 others(16): Show |
19 | HG00140.hp1 HG01069.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-4633delT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64860017 | ||||||
| chr12:64860020 | T | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0090 a0001c0001t0001g0121 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-4648T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860020 | |||||||
| chr12:64860035 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1039-4633T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860035 | |||||||
| chr12:64860036 | A | T | 4 | a0002c0002t0006g0089 a0002c0002t0008g0006 a0002c0002t0008g0052 others(1): Show |
7 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-4632A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860036 | |||||||
| chr12:64860059 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1039-4609A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860059 | |||||||
| chr12:64860132 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG01070.hp2 HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1039-4536C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860132 | |||||||
| chr12:64860192 | A | T | 8 | a0001c0012t0026g0223 a0002c0002t0006g0089 a0002c0002t0008g0006 others(5): Show |
11 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-4476A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860192 | |||||||
| chr12:64860226 | C | A | 1 | a0001c0001t0003g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1039-4442C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860226 | |||||||
| chr12:64860467 | T | A | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-4201T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860467 | |||||||
| chr12:64860470 | C | CT | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-4187dupT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64860470 | ||||||
| chr12:64860859 | G | T | 3 | a0002c0006t0002g0234 a0002c0006t0002g0235 a0002c0006t0002g0237 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1039-3809G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860859 | |||||||
| chr12:64860957 | C | T | 3 | a0001c0001t0003g0066 a0001c0001t0003g0077 a0002c0002t0005g0062 |
3 | HG03516.hp1 NA18948.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1039-3711C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860957 | |||||||
| chr12:64860988 | G | T | 1 | a0002c0002t0010g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1039-3680G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64860988 | |||||||
| chr12:64861164 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1039-3504G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861164 | |||||||
| chr12:64861215 | G | T | 1 | a0002c0003t0006g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1039-3453G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861215 | |||||||
| chr12:64861475 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-3193A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861475 | |||||||
| chr12:64861532 | T | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-3136T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861532 | |||||||
| chr12:64861626 | AT | A | 15 | a0002c0002t0012g0046 a0002c0003t0006g0004 a0002c0003t0006g0037 others(12): Show |
19 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-3033delT | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr12 | 64861626 | ||||||
| chr12:64861646 | G | A | 1 | a0001c0001t0004g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1039-3022G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861646 | |||||||
| chr12:64861673 | C | A | 61 | a0001c0012t0026g0223 a0002c0002t0001g0039 a0002c0002t0001g0217 others(58): Show |
76 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(73): Show |
intron_variant | MODIFIER | c.1039-2995C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861673 | |||||||
| chr12:64861860 | C | G | 1 | a0002c0002t0006g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1039-2808C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861860 | |||||||
| chr12:64861894 | A | G | 4 | a0002c0002t0002g0016 a0002c0002t0002g0068 a0002c0002t0002g0116 others(1): Show |
5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-2774A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861894 | |||||||
| chr12:64861973 | C | T | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-2695C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861973 | |||||||
| chr12:64861981 | C | T | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1039-2687C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64861981 | |||||||
| chr12:64862456 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
6 | HG00735.hp2 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-2212G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862456 | |||||||
| chr12:64862541 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1039-2127G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862541 | |||||||
| chr12:64862651 | A | G | 1 | a0002c0003t0006g0172 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1039-2017A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862651 | |||||||
| chr12:64862709 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1039-1959A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862709 | |||||||
| chr12:64862764 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-1904A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862764 | |||||||
| chr12:64862804 | G | A | 3 | a0002c0006t0002g0234 a0002c0006t0002g0235 a0002c0006t0002g0237 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1039-1864G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862804 | |||||||
| chr12:64862860 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1039-1808C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862860 | |||||||
| chr12:64862915 | C | T | 17 | a0002c0002t0002g0016 a0002c0002t0002g0023 a0002c0002t0002g0030 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039-1753C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64862915 | |||||||
| chr12:64863118 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-1550A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863118 | |||||||
| chr12:64863278 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1039-1390C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863278 | |||||||
| chr12:64863536 | A | C | 1 | a0001c0004t0005g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1039-1132A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863536 | |||||||
| chr12:64863539 | C | T | 2 | a0001c0001t0003g0107 a0001c0001t0003g0113 |
2 | HG00597.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1039-1129C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863539 | |||||||
| chr12:64863540 | G | A | 61 | a0001c0012t0026g0223 a0002c0002t0001g0039 a0002c0002t0001g0217 others(58): Show |
76 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(73): Show |
intron_variant | MODIFIER | c.1039-1128G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863540 | |||||||
| chr12:64863555 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-1113G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863555 | |||||||
| chr12:64863651 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1039-1017A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863651 | |||||||
| chr12:64863670 | A | G | 61 | a0001c0012t0026g0223 a0002c0002t0001g0039 a0002c0002t0001g0217 others(58): Show |
76 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(73): Show |
intron_variant | MODIFIER | c.1039-998A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863670 | |||||||
| chr12:64863675 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-993G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863675 | |||||||
| chr12:64863892 | A | G | 4 | a0002c0002t0012g0046 a0002c0006t0002g0234 a0002c0006t0002g0235 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-776A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64863892 | |||||||
| chr12:64864344 | C | T | 4 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(1): Show |
7 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-324C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64864344 | |||||||
| chr12:64864356 | T | C | 6 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(3): Show |
7 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-312T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64864356 | |||||||
| chr12:64864490 | C | T | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1039-178C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 8/11 | chr12 | 64864490 | |||||||
| chr12:64864811 | T | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1151+31T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64864811 | |||||||
| chr12:64865102 | G | A | 1 | a0001c0004t0005g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1151+322G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865102 | |||||||
| chr12:64865180 | T | C | 8 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0007g0002 others(5): Show |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1151+400T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865180 | |||||||
| chr12:64865488 | G | A | 3 | a0002c0006t0002g0234 a0002c0006t0002g0235 a0002c0006t0002g0237 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1151+708G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865488 | |||||||
| chr12:64865553 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0020 |
4 | NA18942.hp1 NA18961.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151+773C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865553 | |||||||
| chr12:64865554 | G | A | 4 | a0002c0002t0002g0023 a0002c0002t0002g0168 a0002c0002t0002g0169 others(1): Show |
5 | HG02145.hp1 HG02486.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151+774G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865554 | |||||||
| chr12:64865594 | G | A | 34 | a0001c0001t0001g0177 a0001c0001t0002g0007 a0001c0001t0002g0093 others(31): Show |
40 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1151+814G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865594 | |||||||
| chr12:64865766 | G | A | 1 | a0002c0002t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1151+986G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865766 | |||||||
| chr12:64865808 | A | T | 2 | a0001c0001t0003g0066 a0001c0001t0003g0077 |
2 | NA18948.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1152-956A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865808 | |||||||
| chr12:64865827 | A | G | 2 | a0002c0003t0006g0231 a0002c0003t0006g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1152-937A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865827 | |||||||
| chr12:64865898 | G | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1152-866G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64865898 | |||||||
| chr12:64866021 | C | A | 1 | a0002c0002t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1152-743C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866021 | |||||||
| chr12:64866025 | G | A | 3 | a0002c0002t0013g0103 a0002c0002t0013g0226 a0002c0002t0013g0227 |
3 | HG02280.hp1 HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1152-739G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866025 | |||||||
| chr12:64866159 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1152-605G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866159 | |||||||
| chr12:64866168 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1152-596G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866168 | |||||||
| chr12:64866217 | G | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1152-547G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866217 | |||||||
| chr12:64866266 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1152-498A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866266 | |||||||
| chr12:64866458 | C | T | 1 | a0002c0002t0020g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1152-306C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866458 | |||||||
| chr12:64866463 | T | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(30): Show |
42 | HG00099.hp1 HG00140.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1152-301T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866463 | |||||||
| chr12:64866499 | C | T | 1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1152-265C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866499 | |||||||
| chr12:64866539 | G | A | 2 | a0002c0005t0012g0032 a0002c0005t0012g0240 |
3 | HG02630.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1152-225G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866539 | |||||||
| chr12:64866561 | C | T | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1152-203C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866561 | |||||||
| chr12:64866757 | T | A | 2 | a0002c0002t0002g0030 a0002c0002t0002g0221 |
3 | HG03041.hp2 HG03486.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.1152-7T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 9/11 | chr12 | 64866757 | |||||||
| chr12:64867145 | C | G | 5 | a0002c0002t0007g0002 a0002c0002t0007g0041 a0002c0002t0007g0043 others(2): Show |
9 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1291+242C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867145 | |||||||
| chr12:64867199 | C | T | 4 | a0001c0001t0004g0182 a0001c0001t0004g0193 a0001c0001t0004g0196 others(1): Show |
4 | NA18946.hp2 NA18953.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+296C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867199 | |||||||
| chr12:64867330 | C | T | 15 | a0002c0002t0028g0082 a0002c0003t0006g0004 a0002c0003t0006g0037 others(12): Show |
19 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1291+427C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867330 | |||||||
| chr12:64867459 | C | CA | 14 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0007g0002 others(11): Show |
19 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1291+571dupA | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 64867459 | ||||||
| chr12:64867459 | CA | C | 7 | a0001c0001t0003g0107 a0001c0001t0003g0113 a0001c0001t0004g0208 others(4): Show |
7 | HG00597.hp1 HG01361.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+571delA | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 64867459 | ||||||
| chr12:64867459 | CAA | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291+570_1291+571d others(4): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 64867459 | ||||||
| chr12:64867482 | T | A | 1 | a0001c0001t0011g0026 | 2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1291+579T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867482 | |||||||
| chr12:64867547 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291+644G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867547 | |||||||
| chr12:64867582 | A | C | 8 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0007g0002 others(5): Show |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1291+679A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867582 | |||||||
| chr12:64867616 | T | A | 1 | a0001c0001t0002g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1291+713T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867616 | |||||||
| chr12:64867818 | A | G | 1 | a0002c0002t0008g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1291+915A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867818 | |||||||
| chr12:64867827 | G | A | 53 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0002g0016 others(50): Show |
65 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(62): Show |
intron_variant | MODIFIER | c.1291+924G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867827 | |||||||
| chr12:64867851 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1291+948T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867851 | |||||||
| chr12:64867855 | C | G | 8 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0007g0002 others(5): Show |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1291+952C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64867855 | |||||||
| chr12:64868213 | C | T | 1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1291+1310C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868213 | |||||||
| chr12:64868215 | A | G | 1 | a0002c0002t0028g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+1312A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868215 | |||||||
| chr12:64868268 | G | A | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1291+1365G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868268 | |||||||
| chr12:64868332 | A | G | 3 | a0001c0001t0001g0065 a0002c0002t0002g0016 a0002c0002t0002g0116 |
4 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+1429A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868332 | |||||||
| chr12:64868551 | A | G | 2 | a0001c0001t0004g0191 a0001c0001t0004g0208 |
2 | NA19059.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1291+1648A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868551 | |||||||
| chr12:64868625 | A | T | 1 | a0001c0001t0004g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1291+1722A>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868625 | |||||||
| chr12:64868664 | A | G | 5 | a0002c0002t0007g0002 a0002c0002t0007g0041 a0002c0002t0007g0043 others(2): Show |
9 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1291+1761A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868664 | |||||||
| chr12:64868688 | G | A | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1291+1785G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868688 | |||||||
| chr12:64868740 | C | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291+1837C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868740 | |||||||
| chr12:64868751 | C | G | 5 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(2): Show |
6 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+1848C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868751 | |||||||
| chr12:64868815 | A | G | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-1787A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64868815 | |||||||
| chr12:64869172 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1292-1430C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64869172 | |||||||
| chr12:64869659 | G | T | 20 | a0001c0001t0004g0008 a0001c0001t0004g0072 a0001c0001t0004g0180 others(17): Show |
24 | HG01175.hp2 HG01361.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1292-943G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64869659 | |||||||
| chr12:64869660 | C | T | 20 | a0001c0001t0004g0008 a0001c0001t0004g0072 a0001c0001t0004g0180 others(17): Show |
24 | HG01175.hp2 HG01361.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1292-942C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64869660 | |||||||
| chr12:64870048 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1292-554G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64870048 | |||||||
| chr12:64870310 | C | T | 67 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(64): Show |
83 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(80): Show |
intron_variant | MODIFIER | c.1292-292C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64870310 | |||||||
| chr12:64870516 | C | T | 13 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0005g0062 others(10): Show |
17 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1292-86C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64870516 | |||||||
| chr12:64870580 | A | G | 1 | a0001c0001t0004g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1292-22A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 10/11 | chr12 | 64870580 | |||||||
| chr12:64871145 | A | C | 8 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498+337A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64871145 | |||||||
| chr12:64871168 | A | AG | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1498+360_1498+361i others(3): Show |
TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64871168 | |||||||
| chr12:64871854 | T | A | 1 | a0002c0002t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1498+1046T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64871854 | |||||||
| chr12:64871907 | C | T | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1498+1099C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64871907 | |||||||
| chr12:64871910 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1498+1102T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64871910 | |||||||
| chr12:64871937 | G | A | 1 | a0004c0008t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1498+1129G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64871937 | |||||||
| chr12:64872186 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1498+1378C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872186 | |||||||
| chr12:64872193 | G | A | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1498+1385G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872193 | |||||||
| chr12:64872210 | T | G | 5 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(2): Show |
6 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498+1402T>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872210 | |||||||
| chr12:64872232 | T | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1498+1424T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872232 | |||||||
| chr12:64872361 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1498+1553C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872361 | |||||||
| chr12:64872525 | T | A | 66 | a0001c0001t0009g0012 a0001c0001t0009g0054 a0001c0001t0009g0055 others(63): Show |
82 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(79): Show |
intron_variant | MODIFIER | c.1498+1717T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872525 | |||||||
| chr12:64872637 | G | C | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1498+1829G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872637 | |||||||
| chr12:64872679 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1498+1871G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872679 | |||||||
| chr12:64872897 | T | C | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1498+2089T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872897 | |||||||
| chr12:64872980 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0002g0097 |
2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1499-2021G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64872980 | |||||||
| chr12:64873110 | G | C | 1 | a0001c0001t0004g0192 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1499-1891G>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873110 | |||||||
| chr12:64873485 | G | A | 14 | a0002c0003t0006g0004 a0002c0003t0006g0037 a0002c0003t0006g0038 others(11): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1499-1516G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873485 | |||||||
| chr12:64873510 | C | G | 1 | a0002c0002t0007g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1499-1491C>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873510 | |||||||
| chr12:64873719 | A | C | 8 | a0001c0012t0026g0223 a0002c0002t0006g0089 a0002c0002t0008g0006 others(5): Show |
11 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1499-1282A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873719 | |||||||
| chr12:64873787 | G | T | 1 | a0001c0001t0003g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1499-1214G>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873787 | |||||||
| chr12:64873822 | T | A | 8 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(5): Show |
9 | HG01884.hp2 HG02622.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1499-1179T>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873822 | |||||||
| chr12:64873823 | C | A | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1499-1178C>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873823 | |||||||
| chr12:64873931 | C | T | 1 | a0002c0002t0005g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1499-1070C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64873931 | |||||||
| chr12:64874115 | G | A | 1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1499-886G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874115 | |||||||
| chr12:64874153 | A | G | 8 | a0002c0002t0001g0039 a0002c0002t0001g0217 a0002c0002t0007g0002 others(5): Show |
12 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1499-848A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874153 | |||||||
| chr12:64874430 | C | T | 3 | a0002c0006t0002g0234 a0002c0006t0002g0235 a0002c0006t0002g0237 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1499-571C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874430 | |||||||
| chr12:64874450 | G | A | 1 | a0002c0006t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1499-551G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874450 | |||||||
| chr12:64874469 | A | C | 3 | a0002c0005t0006g0238 a0002c0005t0006g0239 a0002c0010t0006g0236 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1499-532A>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874469 | |||||||
| chr12:64874613 | C | T | 4 | a0002c0002t0010g0013 a0002c0002t0010g0057 a0002c0002t0010g0058 others(1): Show |
5 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-388C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874613 | |||||||
| chr12:64874614 | A | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0115 others(8): Show |
12 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1499-387A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874614 | |||||||
| chr12:64874660 | A | G | 1 | a0002c0002t0012g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1499-341A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874660 | |||||||
| chr12:64874807 | C | T | 1 | a0005c0009t0029g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1499-194C>T | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874807 | |||||||
| chr12:64874856 | A | G | 1 | a0002c0002t0002g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1499-145A>G | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874856 | |||||||
| chr12:64874882 | G | A | 2 | a0002c0005t0012g0032 a0002c0005t0012g0240 |
3 | HG02630.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1499-119G>A | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874882 | |||||||
| chr12:64874957 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1499-44T>C | TBC1D30 | ENSG00000111490.15 | transcript | ENST00000539867.6 | protein_coding | 11/11 | chr12 | 64874957 |