Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23158 |
|---|---|
| ensemblid | ENSG00000109436.8 |
| hgncid | 21710 |
| symbol | TBC1D9 |
| name | TBC1 domain family member 9 |
| refseq_nuc | NM_015130.3 |
| refseq_prot | NP_055945.2 |
| ensembl_nuc | ENST00000442267.3 |
| ensembl_prot | ENSP00000411197.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 140620782 |
| end | 140756385 |
| strand | - |
| ver | v1.2 |
| region | chr4:140620782-140756385 |
| region5000 | chr4:140615782-140761385 |
| regionname0 | TBC1D9_chr4_140620782_140756385 |
| regionname5000 | TBC1D9_chr4_140615782_140761385 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1266 | 291 | 86 | 63 | 104 | 10 | 26 | 80 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0002 | 0/0 | 1266 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0003 | 0/0 | 1266 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3801 | 125 | 37 | 26 | 38 | 6 | 17 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0002 | 0/0 | 3801 | 59 | 14 | 21 | 17 | 3 | 4 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0003 | 0/0 | 3801 | 27 | 2 | 3 | 20 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0004 | 0/0 | 3801 | 24 | 7 | 6 | 9 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0005 | 0/0 | 3801 | 15 | 11 | 2 | 0 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0006 | 1/0 | 3801 | 12 | 1 | 1 | 9 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0007 | 0/0 | 3801 | 8 | 0 | 0 | 8 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0008 | 0/0 | 3801 | 8 | 7 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0009 | 0/0 | 3801 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0010 | 0/0 | 3801 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0011 | 0/0 | 3801 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0012 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0013 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0014 | 0/0 | 3801 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0015 | 0/0 | 3801 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0016 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0017 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0018 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0019 | 0/0 | 3801 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0020 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| c0021 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1754 | 225 | 63 | 46 | 85 | 9 | 21 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0002 | 0/1 | 1754 | 34 | 9 | 8 | 12 | 1 | 3 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0003 | 0/0 | 1754 | 14 | 3 | 7 | 3 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0004 | 0/0 | 1754 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0005 | 0/0 | 1754 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0006 | 0/0 | 1754 | 3 | 2 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0007 | 0/0 | 1754 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0008 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0009 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0010 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0011 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0012 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0013 | 0/0 | 1754 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0014 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0015 | 0/0 | 1754 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0016 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| t0017 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3801 | 125 | 37 | 26 | 38 | 6 | 17 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002 | 0/0 | 3801 | 59 | 14 | 21 | 17 | 3 | 4 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0003 | 0/0 | 3801 | 27 | 2 | 3 | 20 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0004 | 0/0 | 3801 | 24 | 7 | 6 | 9 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0005 | 0/0 | 3801 | 15 | 11 | 2 | 0 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0006 | 1/0 | 3801 | 12 | 1 | 1 | 9 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0007 | 0/0 | 3801 | 8 | 0 | 0 | 8 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0008 | 0/0 | 3801 | 8 | 7 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0010 | 0/0 | 3801 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0011 | 0/0 | 3801 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0012 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0013 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0014 | 0/0 | 3801 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0015 | 0/0 | 3801 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0016 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0017 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0018 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0020 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0021 | 0/0 | 3801 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0002c0009 | 0/0 | 3801 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0003c0019 | 0/0 | 3801 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5554 | 94 | 27 | 21 | 26 | 5 | 15 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0002 | 0/1 | 5554 | 12 | 6 | 1 | 2 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0003 | 0/0 | 5554 | 8 | 0 | 4 | 3 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0004 | 0/0 | 5554 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0005 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0006 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0010 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0014 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0016 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0001t0017 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002t0001 | 0/0 | 5554 | 46 | 11 | 13 | 16 | 3 | 3 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002t0002 | 0/0 | 5554 | 5 | 1 | 3 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002t0003 | 0/0 | 5554 | 4 | 1 | 3 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002t0006 | 0/0 | 5554 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002t0013 | 0/0 | 5554 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0002t0015 | 0/0 | 5554 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0003t0001 | 0/0 | 5554 | 25 | 1 | 3 | 19 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0003t0003 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0003t0007 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0004t0001 | 0/0 | 5554 | 19 | 5 | 5 | 7 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0004t0002 | 0/0 | 5554 | 4 | 1 | 1 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0004t0005 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0005t0001 | 0/0 | 5554 | 10 | 10 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0005t0002 | 0/0 | 5554 | 4 | 0 | 2 | 0 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0005t0009 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0006t0001 | 1/0 | 5554 | 11 | 1 | 1 | 8 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0006t0007 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0007t0001 | 0/0 | 5554 | 7 | 0 | 0 | 7 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0007t0007 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0008t0001 | 0/0 | 5554 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0008t0002 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0008t0003 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0008t0005 | 0/0 | 5554 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0010t0001 | 0/0 | 5554 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0011t0001 | 0/0 | 5554 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0012t0008 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0013t0011 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0014t0001 | 0/0 | 5554 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0015t0002 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0016t0012 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0017t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0018t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0020t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0001c0021t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0002c0009t0002 | 0/0 | 5554 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| a0003c0019t0002 | 0/0 | 5554 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | copy fasta | chr4 | 140615782 | 140761385 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0016g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0001t0017g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0006g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0013g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0002t0015g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0003t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0004t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0005t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0001g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0006t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0007t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0008t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0010t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0010t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0011t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0012t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0013t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0014t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0015t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0016t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0017t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0018t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0020t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0001c0021t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0002c0009t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0002c0009t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0002c0009t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0002c0009t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0002c0009t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0002c0009t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| a0003c0019t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0096 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0188 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00639 | hp1 | a0001 | c0005 | t0002 | g0127 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0164 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00735 | hp2 | a0001 | c0004 | t0002 | g0126 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0135 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0123 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0125 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01074 | hp1 | a0003 | c0019 | t0002 | g0124 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0281 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0275 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01256 | hp1 | a0001 | c0011 | t0001 | g0001 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0172 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01258 | hp2 | a0001 | c0011 | t0001 | g0001 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01261 | hp2 | a0001 | c0008 | t0005 | g0241 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0225 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0283 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01361 | hp2 | a0001 | c0014 | t0001 | g0088 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01884 | hp1 | a0001 | c0002 | t0006 | g0099 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0255 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0136 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0168 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0224 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0114 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02155 | hp2 | a0001 | c0006 | t0007 | g0227 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0216 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02258 | hp1 | a0001 | c0017 | t0001 | g0158 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0297 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02280 | hp2 | a0001 | c0008 | t0001 | g0179 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02300 | hp1 | a0001 | c0005 | t0002 | g0130 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02300 | hp2 | a0001 | c0002 | t0013 | g0252 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02451 | hp2 | a0001 | c0008 | t0001 | g0183 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0091 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0285 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0128 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0132 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02647 | hp2 | a0001 | c0008 | t0002 | g0186 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0284 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02723 | hp2 | a0001 | c0005 | t0009 | g0004 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0110 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02809 | hp1 | a0001 | c0008 | t0005 | g0178 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02886 | hp1 | a0001 | c0013 | t0011 | g0115 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0157 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02896 | hp2 | a0001 | c0004 | t0005 | g0265 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0145 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0171 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03041 | hp2 | a0001 | c0008 | t0003 | g0276 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0193 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0185 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0142 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03225 | hp1 | a0001 | c0012 | t0008 | g0146 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0159 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0228 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03491 | hp1 | a0001 | c0005 | t0002 | g0102 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03492 | hp2 | a0001 | c0005 | t0002 | g0101 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0260 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG04228 | hp1 | a0001 | c0002 | t0015 | g0280 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0129 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18944 | hp2 | a0001 | c0006 | t0001 | g0235 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18963 | hp2 | a0001 | c0007 | t0001 | g0219 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18964 | hp1 | a0001 | c0004 | t0002 | g0017 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18966 | hp1 | a0002 | c0009 | t0002 | g0047 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18966 | hp2 | a0001 | c0006 | t0001 | g0210 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18967 | hp2 | a0001 | c0006 | t0001 | g0257 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18972 | hp2 | a0001 | c0006 | t0001 | g0261 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18973 | hp1 | a0001 | c0007 | t0001 | g0170 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18979 | hp2 | a0001 | c0006 | t0001 | g0263 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18981 | hp1 | a0001 | c0007 | t0007 | g0106 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18982 | hp1 | a0002 | c0009 | t0002 | g0036 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18984 | hp1 | a0001 | c0007 | t0001 | g0238 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18984 | hp2 | a0002 | c0009 | t0002 | g0046 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18988 | hp1 | a0002 | c0009 | t0002 | g0120 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18988 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18989 | hp1 | a0001 | c0003 | t0007 | g0012 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18989 | hp2 | a0001 | c0007 | t0001 | g0218 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18990 | hp1 | a0001 | c0007 | t0001 | g0118 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0055 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18991 | hp2 | a0001 | c0001 | t0016 | g0295 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18993 | hp2 | a0001 | c0007 | t0001 | g0254 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA18995 | hp2 | a0001 | c0015 | t0002 | g0084 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19009 | hp1 | a0001 | c0006 | t0001 | g0205 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19011 | hp1 | a0001 | c0007 | t0001 | g0229 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19043 | hp1 | a0001 | c0008 | t0001 | g0240 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19056 | hp2 | a0001 | c0010 | t0001 | g0259 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19057 | hp2 | a0001 | c0010 | t0001 | g0190 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19063 | hp1 | a0002 | c0009 | t0002 | g0039 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19064 | hp1 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19067 | hp2 | a0001 | c0006 | t0001 | g0258 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19079 | hp2 | a0001 | c0006 | t0001 | g0029 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19083 | hp1 | a0001 | c0001 | t0010 | g0054 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19084 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19088 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19091 | hp2 | a0002 | c0009 | t0002 | g0048 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0152 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0133 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ASW | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20129 | hp2 | a0001 | c0021 | t0001 | g0264 | AFR | ASW | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0221 | EUR | TSI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | GIH | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0113 | SAS | GIH | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG01123 | hp2 | a0001 | c0006 | t0001 | g0018 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0272 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02559 | hp1 | a0001 | c0016 | t0012 | g0271 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0290 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0086 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG06807 | hp1 | a0001 | c0020 | t0001 | g0187 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA20300 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| NA21309 | hp2 | a0001 | c0018 | t0001 | g0174 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0105 | REF | REF | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| homoSapiens_grch38 | hp1 | a0001 | c0006 | t0001 | g0273 | REF | REF | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140622761
|
C | T | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.3235G>A | p.Gly1079Arg | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3575/5554 | 3235/3801 | 1079/1266 | chr4 | 140622761 | ||
| chr4:140622862
|
T | C | 1 | a0002 | 6 | NA18966.hp1 NA18982.hp1 NA18984.hp2 others(3): Show |
missense_variant | MODERATE | c.3134A>G | p.Asn1045Ser | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3474/5554 | 3134/3801 | 1045/1266 | chr4 | 140622862 | ||
| chr4:140662084
|
G | A | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1612C>T | p.His538Tyr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/21 | 1952/5554 | 1612/3801 | 538/1266 | chr4 | 140662084 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140622435
|
C | T | 1 | a0001c0016 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.3561G>A | p.Thr1187Thr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3901/5554 | 3561/3801 | 1187/1266 | chr4 | 140622435 | ||
| chr4:140622741
|
C | T | 2 | a0001c0013a0001c0017 | 2 | HG02258.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.3255G>A | p.Pro1085Pro | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3595/5554 | 3255/3801 | 1085/1266 | chr4 | 140622741 | ||
| chr4:140622810
|
C | T | 1 | a0001c0012 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.3186G>A | p.Glu1062Glu | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3526/5554 | 3186/3801 | 1062/1266 | chr4 | 140622810 | ||
| chr4:140622843
|
G | A | 15 | a0001c0001a0001c0002a0001c0004others(12): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
synonymous_variant | LOW | c.3153C>T | p.His1051His | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3493/5554 | 3153/3801 | 1051/1266 | chr4 | 140622843 | ||
| chr4:140639342
|
C | T | 1 | a0001c0016 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.2424G>A | p.Thr808Thr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 14/21 | 2764/5554 | 2424/3801 | 808/1266 | chr4 | 140639342 | ||
| chr4:140639423
|
G | A | 1 | a0001c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2343C>T | p.Phe781Phe | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 14/21 | 2683/5554 | 2343/3801 | 781/1266 | chr4 | 140639423 | ||
| chr4:140657802
|
C | T | 1 | a0001c0015 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.1932G>A | p.Val644Val | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 12/21 | 2272/5554 | 1932/3801 | 644/1266 | chr4 | 140657802 | ||
| chr4:140662022
|
C | T | 3 | a0001c0005a0001c0008a0001c0014 | 24 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(21): Show |
synonymous_variant | LOW | c.1674G>A | p.Glu558Glu | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/21 | 2014/5554 | 1674/3801 | 558/1266 | chr4 | 140662022 | ||
| chr4:140668981
|
C | T | 1 | a0001c0011 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.1524G>A | p.Thr508Thr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/21 | 1864/5554 | 1524/3801 | 508/1266 | chr4 | 140668981 | ||
| chr4:140676972
|
C | T | 6 | a0001c0004a0001c0007a0001c0012others(3): Show | 41 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(38): Show |
synonymous_variant | LOW | c.981G>A | p.Gln327Gln | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/21 | 1321/5554 | 981/3801 | 327/1266 | chr4 | 140676972 | ||
| chr4:140679166
|
A | G | 15 | a0001c0001a0001c0003a0001c0004others(12): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
synonymous_variant | LOW | c.627T>C | p.Leu209Leu | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/21 | 967/5554 | 627/3801 | 209/1266 | chr4 | 140679166 | ||
| chr4:140679760
|
A | G | 1 | a0001c0010 | 2 | NA19056.hp2 NA19057.hp2 |
synonymous_variant | LOW | c.444T>C | p.Phe148Phe | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/21 | 784/5554 | 444/3801 | 148/1266 | chr4 | 140679760 | ||
| chr4:140701511
|
G | A | 2 | a0001c0020a0001c0021 | 2 | HG06807.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.234C>T | p.Ile78Ile | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/21 | 574/5554 | 234/3801 | 78/1266 | chr4 | 140701511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140621012
|
C | T | 1 | a0001c0013t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 1183 | chr4 | 140621012 | |||||
| chr4:140621116
|
G | C | 2 | a0001c0001t0006a0001c0002t0006 | 3 | HG00735.hp1 HG01884.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1079C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 1079 | chr4 | 140621116 | |||||
| chr4:140621218
|
T | G | 1 | a0001c0016t0012 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 977 | chr4 | 140621218 | |||||
| chr4:140621336
|
C | G | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0015others(6): Show | 35 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*859G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 859 | chr4 | 140621336 | |||||
| chr4:140621604
|
C | T | 4 | a0001c0001t0005a0001c0001t0014a0001c0004t0005others(1): Show | 5 | HG01261.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*591G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 591 | chr4 | 140621604 | |||||
| chr4:140621731
|
C | T | 1 | a0001c0001t0010 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*464G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 464 | chr4 | 140621731 | |||||
| chr4:140621900
|
A | C | 1 | a0001c0005t0009 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 295 | chr4 | 140621900 | |||||
| chr4:140621908
|
A | G | 1 | a0001c0012t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 287 | chr4 | 140621908 | |||||
| chr4:140621985
|
T | A | 3 | a0001c0003t0007a0001c0006t0007a0001c0007t0007 | 3 | HG02155.hp2 NA18981.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*210A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 210 | chr4 | 140621985 | |||||
| chr4:140622046
|
T | C | 1 | a0001c0002t0013 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 149 | chr4 | 140622046 | |||||
| chr4:140622082
|
C | T | 1 | a0001c0001t0016 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 113 | chr4 | 140622082 | |||||
| chr4:140756096
|
G | A | 2 | a0001c0001t0004a0001c0001t0016 | 6 | NA18963.hp1 NA18991.hp2 NA19067.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/21 | 51 | chr4 | 140756096 | |||||
| chr4:140756171
|
G | A | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0014others(5): Show | 22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-126C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/21 | 126 | chr4 | 140756171 | |||||
| chr4:140756194
|
G | A | 1 | a0001c0001t0017 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/21 | 149 | chr4 | 140756194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140623034
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3079-117G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623034 | ||||||
| chr4:140623124
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0177 | 3 | HG01106.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3079-207C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623124 | ||||||
| chr4:140623230
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0177 | 2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3079-313A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623230 | ||||||
| chr4:140623259
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3079-342C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623259 | ||||||
| chr4:140623265
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3079-348G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623265 | ||||||
| chr4:140623350
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3079-433C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623350 | ||||||
| chr4:140623362
|
C | T | 57 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(54): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.3079-445G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623362 | ||||||
| chr4:140623453
|
C | T | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3079-536G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623453 | ||||||
| chr4:140623455
|
A | G | 2 | a0001c0001t0002g0156a0001c0001t0002g0250 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3079-538T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623455 | ||||||
| chr4:140623619
|
C | T | 2 | a0001c0005t0002g0101a0001c0005t0002g0102 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3078+497G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623619 | ||||||
| chr4:140623837
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0059 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3078+279C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623837 | ||||||
| chr4:140623937
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0266 | 2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3078+179G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623937 | ||||||
| chr4:140624007
|
C | CAA | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.3078+108_3078+109i others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140624007 | ||||||
| chr4:140624089
|
C | G | 1 | a0001c0006t0007g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3078+27G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140624089 | ||||||
| chr4:140624222
|
A | G | 3 | a0001c0005t0001g0131a0001c0005t0001g0145a0001c0005t0001g0157 | 3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.2975-3T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 19/20 | chr4 | 140624222 | ||||||
| chr4:140624243
|
A | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.2975-24T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 19/20 | chr4 | 140624243 | ||||||
| chr4:140624410
|
G | GA | 35 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0034others(32): Show | 35 | HG00733.hp2 HG00741.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.2900-23dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624410 | ||||||
| chr4:140624445
|
AT | A | 22 | a0001c0001t0002g0013a0001c0001t0002g0043a0001c0001t0002g0066others(19): Show | 22 | HG00639.hp2 HG01074.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2900-58delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624445 | ||||||
| chr4:140624499
|
GCAAA | G | 17 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2900-115_2900-112d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624499 | ||||||
| chr4:140624512
|
CA | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.2900-125delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624512 | ||||||
| chr4:140624717
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0266a0001c0004t0001g0272 | 3 | HG02451.hp1 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2900-329C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624717 | ||||||
| chr4:140624876
|
A | T | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2900-488T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624876 | ||||||
| chr4:140625052
|
CA | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2900-665delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625052 | ||||||
| chr4:140625267
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2900-879T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625267 | ||||||
| chr4:140625391
|
C | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2900-1003G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625391 | ||||||
| chr4:140625430
|
G | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0051others(4): Show | 7 | NA18948.hp2 NA18963.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.2900-1042C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625430 | ||||||
| chr4:140625491
|
C | T | 1 | a0001c0004t0005g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2900-1103G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625491 | ||||||
| chr4:140625502
|
C | T | 2 | a0001c0002t0001g0188a0001c0002t0001g0199 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.2900-1114G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625502 | ||||||
| chr4:140625937
|
G | A | 2 | a0001c0003t0001g0193a0001c0021t0001g0264 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2899+1504C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625937 | ||||||
| chr4:140626150
|
G | A | 34 | a0001c0001t0002g0013a0001c0001t0002g0038a0001c0001t0002g0043others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.2899+1291C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626150 | ||||||
| chr4:140626276
|
A | G | 4 | a0001c0001t0002g0274a0001c0005t0002g0127a0001c0005t0002g0130others(1): Show | 4 | HG00639.hp1 HG02300.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2899+1165T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626276 | ||||||
| chr4:140626282
|
GC | G | 8 | a0001c0003t0001g0041a0001c0003t0001g0055a0001c0003t0001g0078others(5): Show | 8 | HG00621.hp1 NA18943.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.2899+1158delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626282 | ||||||
| chr4:140626293
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2899+1148G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626293 | ||||||
| chr4:140626775
|
C | T | 1 | a0001c0013t0011g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2899+666G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626775 | ||||||
| chr4:140626843
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2899+598C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626843 | ||||||
| chr4:140626927
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0177 | 3 | HG01106.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2899+514T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626927 | ||||||
| chr4:140626958
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2899+483A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626958 | ||||||
| chr4:140627059
|
T | G | 3 | a0001c0001t0014g0284a0001c0008t0005g0178a0001c0008t0005g0241 | 3 | HG01261.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2899+382A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140627059 | ||||||
| chr4:140627415
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2899+26A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140627415 | ||||||
| chr4:140627769
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.2813-242T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140627769 | ||||||
| chr4:140627838
|
G | T | 1 | a0001c0002t0001g0234 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2813-311C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140627838 | ||||||
| chr4:140627875
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2813-348G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140627875 | ||||||
| chr4:140628016
|
C | G | 4 | a0001c0001t0001g0237a0001c0002t0001g0267a0001c0002t0001g0268others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2812+284G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628016 | ||||||
| chr4:140628199
|
G | A | 1 | a0001c0004t0001g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2812+101C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628199 | ||||||
| chr4:140628239
|
C | A | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2812+61G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628239 | ||||||
| chr4:140628274
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2812+26T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628274 | ||||||
| chr4:140628660
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2747-295G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140628660 | ||||||
| chr4:140628661
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2747-296C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140628661 | ||||||
| chr4:140628843
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2747-478T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140628843 | ||||||
| chr4:140629021
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2747-656T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629021 | ||||||
| chr4:140629280
|
G | A | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(11): Show | 14 | HG01069.hp2 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2747-915C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629280 | ||||||
| chr4:140629303
|
G | A | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2747-938C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629303 | ||||||
| chr4:140629378
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2747-1013A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629378 | ||||||
| chr4:140629853
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2747-1488T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629853 | ||||||
| chr4:140629925
|
A | G | 5 | a0001c0003t0001g0030a0001c0003t0001g0071a0001c0003t0001g0073others(2): Show | 5 | HG00558.hp1 HG00673.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2747-1560T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629925 | ||||||
| chr4:140629977
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2747-1612A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629977 | ||||||
| chr4:140630454
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2747-2089T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630454 | ||||||
| chr4:140630496
|
G | T | 57 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(54): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2747-2131C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630496 | ||||||
| chr4:140630533
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2747-2168T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630533 | ||||||
| chr4:140630570
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2747-2205C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630570 | ||||||
| chr4:140630645
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2747-2280C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630645 | ||||||
| chr4:140630650
|
G | A | 3 | a0001c0005t0001g0131a0001c0005t0001g0145a0001c0005t0001g0157 | 3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2747-2285C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630650 | ||||||
| chr4:140630779
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0177 | 2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2747-2414T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630779 | ||||||
| chr4:140630866
|
T | C | 4 | a0001c0001t0001g0248a0001c0002t0001g0064a0001c0002t0001g0094others(1): Show | 4 | NA18971.hp2 NA18975.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2747-2501A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630866 | ||||||
| chr4:140631060
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2747-2695T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631060 | ||||||
| chr4:140631335
|
G | C | 4 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0171others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2746+2613C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631335 | ||||||
| chr4:140631367
|
C | A | 1 | a0001c0006t0001g0257 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2746+2581G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631367 | ||||||
| chr4:140631383
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2746+2565G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631383 | ||||||
| chr4:140631423
|
G | A | 1 | a0001c0005t0001g0128 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2746+2525C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631423 | ||||||
| chr4:140631434
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2746+2514C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631434 | ||||||
| chr4:140631448
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0034others(26): Show | 29 | HG00733.hp2 HG00741.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2746+2500G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631448 | ||||||
| chr4:140631601
|
CT | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2746+2346delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631601 | ||||||
| chr4:140631667
|
G | A | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2746+2281C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631667 | ||||||
| chr4:140631823
|
C | T | 57 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(54): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2746+2125G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631823 | ||||||
| chr4:140631950
|
C | T | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2746+1998G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631950 | ||||||
| chr4:140631998
|
A | G | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2746+1950T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631998 | ||||||
| chr4:140632087
|
C | T | 3 | a0001c0005t0001g0131a0001c0005t0001g0145a0001c0005t0001g0157 | 3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2746+1861G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632087 | ||||||
| chr4:140632217
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0051others(3): Show | 6 | NA18948.hp2 NA18963.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.2746+1731T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632217 | ||||||
| chr4:140632262
|
G | GT | 164 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2746+1685dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632262 | ||||||
| chr4:140632262
|
G | GTT | 59 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(56): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2746+1684_2746+168 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632262 | ||||||
| chr4:140632262
|
G | GTTTT | 25 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0065others(22): Show | 25 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.2746+1682_2746+168 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632262 | ||||||
| chr4:140632266
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2746+1682A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632266 | ||||||
| chr4:140632302
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2746+1646A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632302 | ||||||
| chr4:140632346
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2746+1602C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632346 | ||||||
| chr4:140632637
|
G | A | 25 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0065others(22): Show | 25 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.2746+1311C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632637 | ||||||
| chr4:140632710
|
G | A | 1 | a0001c0005t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2746+1238C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632710 | ||||||
| chr4:140632861
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2746+1087G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632861 | ||||||
| chr4:140632882
|
G | A | 1 | a0001c0003t0001g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2746+1066C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632882 | ||||||
| chr4:140632991
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.2746+957T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632991 | ||||||
| chr4:140633115
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2746+833G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633115 | ||||||
| chr4:140633265
|
C | T | 1 | a0001c0005t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2746+683G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633265 | ||||||
| chr4:140633418
|
G | A | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2746+530C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633418 | ||||||
| chr4:140633463
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0072others(2): Show | 5 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.2746+485G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633463 | ||||||
| chr4:140633612
|
A | G | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2746+336T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633612 | ||||||
| chr4:140633795
|
G | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2746+153C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633795 | ||||||
| chr4:140633908
|
G | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2746+40C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633908 | ||||||
| chr4:140634301
|
G | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0153a0001c0002t0001g0195others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2506-113C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634301 | ||||||
| chr4:140634361
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2506-173T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634361 | ||||||
| chr4:140634496
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2506-308G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634496 | ||||||
| chr4:140634497
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.2506-309T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634497 | ||||||
| chr4:140634571
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2506-383A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634571 | ||||||
| chr4:140634592
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0177 | 2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2506-404G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634592 | ||||||
| chr4:140634749
|
A | G | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2506-561T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634749 | ||||||
| chr4:140634785
|
A | G | 1 | a0001c0002t0001g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2506-597T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634785 | ||||||
| chr4:140634973
|
T | C | 2 | a0001c0003t0001g0193a0001c0021t0001g0264 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2506-785A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634973 | ||||||
| chr4:140635179
|
G | GA | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0002g0043others(5): Show | 8 | HG00741.hp1 HG01256.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2506-992dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635179 | ||||||
| chr4:140635180
|
A | G | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2506-992T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635180 | ||||||
| chr4:140635248
|
C | T | 23 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(20): Show | 23 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2506-1060G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635248 | ||||||
| chr4:140635258
|
G | A | 57 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(54): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2506-1070C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635258 | ||||||
| chr4:140635315
|
GA | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.2506-1128delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635315 | ||||||
| chr4:140635384
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2506-1196T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635384 | ||||||
| chr4:140635393
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0143a0001c0001t0001g0144others(57): Show | 60 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2506-1205C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635393 | ||||||
| chr4:140635636
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2506-1448A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635636 | ||||||
| chr4:140635721
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2506-1533C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635721 | ||||||
| chr4:140636338
|
A | G | 6 | a0001c0001t0001g0093a0001c0001t0001g0140a0001c0001t0001g0153others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2506-2150T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636338 | ||||||
| chr4:140636534
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2506-2346A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636534 | ||||||
| chr4:140636606
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2506-2418T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636606 | ||||||
| chr4:140636787
|
T | C | 8 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0002t0001g0100others(5): Show | 8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2505+2299A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636787 | ||||||
| chr4:140636880
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2505+2206G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636880 | ||||||
| chr4:140636956
|
G | C | 1 | a0001c0003t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2505+2130C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636956 | ||||||
| chr4:140636969
|
C | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(85): Show | 88 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.2505+2117G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636969 | ||||||
| chr4:140637022
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0177 | 2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2505+2064C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637022 | ||||||
| chr4:140637070
|
A | G | 1 | a0001c0012t0008g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2505+2016T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637070 | ||||||
| chr4:140637121
|
G | A | 1 | a0001c0004t0001g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2505+1965C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637121 | ||||||
| chr4:140637136
|
G | A | 15 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(12): Show | 15 | HG01069.hp2 HG01192.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2505+1950C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637136 | ||||||
| chr4:140637148
|
G | A | 3 | a0001c0005t0001g0131a0001c0005t0001g0145a0001c0005t0001g0157 | 3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2505+1938C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637148 | ||||||
| chr4:140637148
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2505+1938C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637148 | ||||||
| chr4:140637187
|
T | C | 1 | a0001c0004t0001g0272 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2505+1899A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637187 | ||||||
| chr4:140637200
|
A | G | 23 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(20): Show | 23 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2505+1886T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637200 | ||||||
| chr4:140637265
|
G | A | 2 | a0001c0002t0001g0200a0001c0004t0001g0142 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2505+1821C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637265 | ||||||
| chr4:140637357
|
G | GA | 75 | a0001c0001t0001g0007a0001c0001t0001g0143a0001c0001t0001g0144others(72): Show | 75 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.2505+1728dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637357 | ||||||
| chr4:140637420
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.2505+1666A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637420 | ||||||
| chr4:140637463
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2505+1623G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637463 | ||||||
| chr4:140637540
|
C | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(24): Show | 27 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.2505+1546G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637540 | ||||||
| chr4:140637708
|
T | A | 3 | a0001c0005t0001g0131a0001c0005t0001g0145a0001c0005t0001g0157 | 3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2505+1378A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637708 | ||||||
| chr4:140637872
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(20): Show | 23 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.2505+1214C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637872 | ||||||
| chr4:140637997
|
A | G | 2 | a0001c0001t0001g0069a0001c0004t0001g0113 | 2 | NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2505+1089T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637997 | ||||||
| chr4:140638022
|
A | G | 1 | a0001c0003t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2505+1064T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638022 | ||||||
| chr4:140638439
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2505+647G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638439 | ||||||
| chr4:140638459
|
C | G | 1 | a0001c0004t0001g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2505+627G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638459 | ||||||
| chr4:140638535
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0082 | 2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.2505+551T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638535 | ||||||
| chr4:140638612
|
G | A | 1 | a0001c0002t0001g0230 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2505+474C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638612 | ||||||
| chr4:140639446
|
T | C | 1 | a0001c0001t0004g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2338-18A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639446 | ||||||
| chr4:140639583
|
C | CCA | 35 | a0001c0001t0002g0013a0001c0001t0002g0038a0001c0001t0002g0043others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2338-157_2338-156d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639583 | ||||||
| chr4:140639634
|
C | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2338-206G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639634 | ||||||
| chr4:140639704
|
C | T | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2338-276G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639704 | ||||||
| chr4:140639815
|
T | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.2338-387A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639815 | ||||||
| chr4:140639875
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0177 | 3 | HG01106.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2338-447G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639875 | ||||||
| chr4:140639899
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0250 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2338-471G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639899 | ||||||
| chr4:140639996
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0003g0278a0001c0001t0003g0279others(1): Show | 4 | HG01081.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2338-568A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639996 | ||||||
| chr4:140640086
|
A | G | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2338-658T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640086 | ||||||
| chr4:140640199
|
G | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.2338-771C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640199 | ||||||
| chr4:140640300
|
A | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2338-872T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640300 | ||||||
| chr4:140640403
|
G | A | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2338-975C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640403 | ||||||
| chr4:140640447
|
TG | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2338-1020delC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640447 | ||||||
| chr4:140640450
|
G | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0002t0001g0195others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-1022C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640450 | ||||||
| chr4:140640560
|
G | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(22): Show | 25 | HG00408.hp2 HG01106.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.2338-1132C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640560 | ||||||
| chr4:140640684
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2338-1256G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640684 | ||||||
| chr4:140640743
|
A | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(91): Show | 94 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.2338-1315T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640743 | ||||||
| chr4:140640743
|
A | T | 5 | a0001c0001t0005g0095a0001c0001t0014g0284a0001c0004t0005g0265others(2): Show | 5 | HG01261.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-1315T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640743 | ||||||
| chr4:140640785
|
T | C | 2 | a0001c0001t0002g0156a0001c0001t0002g0250 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2338-1357A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640785 | ||||||
| chr4:140640795
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(21): Show | 24 | HG00408.hp2 HG01106.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2338-1367G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640795 | ||||||
| chr4:140640833
|
C | CATTCTTA others(2): Show |
40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(37): Show | 40 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2338-1406_2338-140 others(13): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640833 | ||||||
| chr4:140640868
|
C | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0073 | 2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2338-1440G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640868 | ||||||
| chr4:140640876
|
C | CATATATA others(13): Show |
25 | a0001c0001t0001g0002a0001c0001t0001g0092a0001c0001t0002g0269others(22): Show | 25 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2338-1449_2338-144 others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640876 | ||||||
| chr4:140640876
|
C | CATATATA others(13): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(12): Show | 15 | HG00408.hp2 HG02056.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2338-1449_2338-144 others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640876 | ||||||
| chr4:140640890
|
CTA | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0025others(12): Show | 15 | HG00408.hp2 HG02056.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2338-1464_2338-146 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640890 | ||||||
| chr4:140640921
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(41): Show | 44 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.2338-1493C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640921 | ||||||
| chr4:140641090
|
C | CA | 6 | a0001c0001t0001g0138a0001c0001t0001g0177a0001c0001t0001g0266others(3): Show | 6 | HG01106.hp2 HG01361.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2338-1663dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641090
|
C | CAA | 8 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0006g0141others(5): Show | 8 | HG01069.hp2 HG01192.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2338-1664_2338-166 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641090
|
C | CAAA | 14 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0148others(11): Show | 14 | HG00140.hp1 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2338-1665_2338-166 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641090
|
C | CAAAA | 22 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0035others(19): Show | 22 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-1666_2338-166 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641090
|
C | CAAAAA | 10 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0069others(7): Show | 10 | HG01169.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2338-1667_2338-166 others(9): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641090
|
C | CAAAAAAA others(3): Show |
3 | a0001c0004t0005g0265a0001c0008t0005g0178a0001c0016t0012g0271 | 3 | HG02559.hp1 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2338-1672_2338-166 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641090
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2338-1675_2338-166 others(17): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | ||||||
| chr4:140641096
|
AAAAAAAA others(2): Show |
A | 29 | a0001c0001t0001g0208a0001c0001t0002g0013a0001c0001t0002g0043others(26): Show | 29 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2338-1677_2338-166 others(13): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641096 | ||||||
| chr4:140641097
|
AAAAAAAA others(1): Show |
A | 34 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0065others(31): Show | 34 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2338-1677_2338-167 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641097 | ||||||
| chr4:140641102
|
AAAC | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2338-1677_2338-167 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641102 | ||||||
| chr4:140641103
|
AAC | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0062others(9): Show | 12 | HG00423.hp1 HG01243.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.2338-1677_2338-167 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641103 | ||||||
| chr4:140641104
|
AC | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0031others(40): Show | 43 | HG00544.hp2 HG00621.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.2338-1677delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641104 | ||||||
| chr4:140641105
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0023others(70): Show | 73 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.2338-1677G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641105 | ||||||
| chr4:140641162
|
A | C | 5 | a0001c0001t0005g0095a0001c0001t0014g0284a0001c0004t0005g0265others(2): Show | 5 | HG01261.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-1734T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641162 | ||||||
| chr4:140641282
|
T | G | 1 | a0001c0002t0001g0173 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2338-1854A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641282 | ||||||
| chr4:140641339
|
C | A | 2 | a0001c0001t0002g0269a0001c0017t0001g0158 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2338-1911G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641339 | ||||||
| chr4:140641643
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0002g0182 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2338-2215C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641643 | ||||||
| chr4:140641644
|
G | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2338-2216C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641644 | ||||||
| chr4:140641656
|
G | A | 16 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0270others(13): Show | 16 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2338-2228C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641656 | ||||||
| chr4:140641739
|
A | G | 2 | a0001c0002t0001g0180a0001c0005t0009g0004 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2338-2311T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641739 | ||||||
| chr4:140641831
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2338-2403G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641831 | ||||||
| chr4:140641858
|
C | A | 55 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0019others(52): Show | 55 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2338-2430G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641858 | ||||||
| chr4:140641858
|
C | G | 1 | a0001c0002t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2338-2430G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641858 | ||||||
| chr4:140641950
|
T | C | 1 | a0001c0004t0002g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2338-2522A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641950 | ||||||
| chr4:140641977
|
G | T | 1 | a0001c0006t0001g0205 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2338-2549C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641977 | ||||||
| chr4:140641984
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0002g0182others(3): Show | 6 | HG01255.hp2 HG02300.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2338-2556G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641984 | ||||||
| chr4:140642027
|
A | G | 1 | a0001c0007t0001g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2338-2599T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642027 | ||||||
| chr4:140642454
|
T | C | 1 | a0001c0003t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2338-3026A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642454 | ||||||
| chr4:140642484
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2338-3056A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642484 | ||||||
| chr4:140642490
|
C | G | 3 | a0001c0005t0002g0127a0001c0005t0002g0130a0001c0008t0002g0186 | 3 | HG00639.hp1 HG02300.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2338-3062G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642490 | ||||||
| chr4:140642593
|
A | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 43 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2338-3165T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642593 | ||||||
| chr4:140642691
|
A | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-3263T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642691 | ||||||
| chr4:140642806
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2338-3378A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642806 | ||||||
| chr4:140642838
|
T | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2338-3410A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642838 | ||||||
| chr4:140642842
|
G | A | 2 | a0001c0005t0001g0131a0001c0005t0001g0132 | 2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2338-3414C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642842 | ||||||
| chr4:140642846
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2338-3418C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642846 | ||||||
| chr4:140642861
|
C | A | 1 | a0001c0004t0001g0172 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2338-3433G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642861 | ||||||
| chr4:140643072
|
A | G | 3 | a0001c0005t0002g0127a0001c0005t0002g0130a0001c0008t0002g0186 | 3 | HG00639.hp1 HG02300.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2338-3644T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643072 | ||||||
| chr4:140643388
|
C | T | 12 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0002t0001g0100others(9): Show | 12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2338-3960G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643388 | ||||||
| chr4:140643402
|
C | CCAGGGTG others(2): Show |
252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2338-3975_2338-397 others(13): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643402 | ||||||
| chr4:140643431
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0176others(4): Show | 7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2338-4003C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643431 | ||||||
| chr4:140643556
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4128A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643556 | ||||||
| chr4:140643578
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2338-4150T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643578 | ||||||
| chr4:140643636
|
G | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-4208C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643636 | ||||||
| chr4:140643742
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0181 | 3 | HG03704.hp1 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2338-4314C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643742 | ||||||
| chr4:140643771
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4343C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643771 | ||||||
| chr4:140644122
|
C | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2338-4694G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644122 | ||||||
| chr4:140644194
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4766C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644194 | ||||||
| chr4:140644338
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4910C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644338 | ||||||
| chr4:140644420
|
G | T | 46 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0072others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2338-4992C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644420 | ||||||
| chr4:140644437
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-5009G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644437 | ||||||
| chr4:140644440
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-5012C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644440 | ||||||
| chr4:140644556
|
C | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2338-5128G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644556 | ||||||
| chr4:140644612
|
G | A | 20 | a0001c0001t0001g0161a0001c0001t0001g0266a0001c0001t0002g0089others(17): Show | 20 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2338-5184C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644612 | ||||||
| chr4:140644712
|
C | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0035others(64): Show | 67 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2338-5284G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644712 | ||||||
| chr4:140644716
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0176others(4): Show | 7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2338-5288C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644716 | ||||||
| chr4:140644801
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-5373C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644801 | ||||||
| chr4:140644815
|
G | A | 3 | a0001c0001t0001g0266a0001c0001t0014g0284a0001c0004t0005g0265 | 3 | HG02451.hp1 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2338-5387C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644815 | ||||||
| chr4:140644859
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2338-5431G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644859 | ||||||
| chr4:140644951
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0176others(7): Show | 10 | HG01106.hp2 HG02055.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2338-5523T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644951 | ||||||
| chr4:140644964
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.2338-5536G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644964 | ||||||
| chr4:140644975
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2338-5547C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644975 | ||||||
| chr4:140645017
|
G | T | 1 | a0001c0004t0001g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2338-5589C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645017 | ||||||
| chr4:140645021
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2338-5593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645021 | ||||||
| chr4:140645037
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-5609G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645037 | ||||||
| chr4:140645058
|
C | G | 1 | a0001c0004t0001g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2338-5630G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645058 | ||||||
| chr4:140645235
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02280.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2338-5807C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645235 | ||||||
| chr4:140645458
|
C | T | 1 | a0001c0003t0001g0083 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2338-6030G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645458 | ||||||
| chr4:140645459
|
G | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2338-6031C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645459 | ||||||
| chr4:140645544
|
G | A | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2338-6116C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645544 | ||||||
| chr4:140645701
|
C | G | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2338-6273G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645701 | ||||||
| chr4:140645730
|
C | T | 87 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(84): Show | 87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2338-6302G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645730 | ||||||
| chr4:140645926
|
C | T | 1 | a0001c0003t0007g0012 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2338-6498G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645926 | ||||||
| chr4:140646130
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0270others(5): Show | 8 | HG01261.hp2 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2338-6702C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646130 | ||||||
| chr4:140646201
|
G | T | 1 | a0001c0002t0002g0231 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2338-6773C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646201 | ||||||
| chr4:140646318
|
C | T | 1 | a0001c0004t0001g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2338-6890G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646318 | ||||||
| chr4:140646373
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2338-6945G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646373 | ||||||
| chr4:140646478
|
A | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-7050T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646478 | ||||||
| chr4:140646514
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2338-7086A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646514 | ||||||
| chr4:140646527
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2338-7099A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646527 | ||||||
| chr4:140646847
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | HG03704.hp1 HG03710.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2338-7419C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646847 | ||||||
| chr4:140646851
|
C | T | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2338-7423G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646851 | ||||||
| chr4:140647067
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2338-7639T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647067 | ||||||
| chr4:140647193
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2338-7765G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647193 | ||||||
| chr4:140647466
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2338-8038T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647466 | ||||||
| chr4:140647505
|
C | A | 1 | a0003c0019t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2338-8077G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647505 | ||||||
| chr4:140647658
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(105): Show | 108 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.2338-8230G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647658 | ||||||
| chr4:140647666
|
G | A | 2 | a0001c0002t0001g0196a0001c0002t0001g0197 | 2 | HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2338-8238C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647666 | ||||||
| chr4:140647791
|
T | C | 1 | a0001c0002t0001g0195 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2338-8363A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647791 | ||||||
| chr4:140647824
|
C | T | 1 | a0001c0013t0011g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2338-8396G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647824 | ||||||
| chr4:140647856
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0151 | 3 | HG01884.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2338-8428C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647856 | ||||||
| chr4:140647894
|
TGGGGGTC others(21): Show |
T | 5 | a0001c0001t0001g0072a0001c0003t0001g0071a0001c0003t0001g0073others(2): Show | 5 | HG00408.hp1 HG00673.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-8494_2338-846 others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647894 | ||||||
| chr4:140648231
|
T | C | 11 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0270others(8): Show | 11 | HG01261.hp2 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2338-8803A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648231 | ||||||
| chr4:140648236
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2338-8808C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648236 | ||||||
| chr4:140648385
|
G | GT | 12 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0251others(9): Show | 12 | HG00642.hp2 HG00741.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2337+8711dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648385 | ||||||
| chr4:140648385
|
G | GTT | 13 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0002t0001g0100others(10): Show | 13 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2337+8710_2337+871 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648385 | ||||||
| chr4:140648385
|
G | T | 1 | a0001c0001t0002g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2337+8712C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648385 | ||||||
| chr4:140648387
|
T | TG | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+8709_2337+871 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648387 | ||||||
| chr4:140648388
|
T | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2337+8709A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648388 | ||||||
| chr4:140648542
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+8555G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648542 | ||||||
| chr4:140648567
|
G | A | 7 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0270others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2337+8530C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648567 | ||||||
| chr4:140648630
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0122others(3): Show | 6 | HG01496.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2337+8467G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648630 | ||||||
| chr4:140648693
|
C | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(49): Show | 52 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2337+8404G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648693 | ||||||
| chr4:140648909
|
GC | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0035others(65): Show | 68 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2337+8187delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648909 | ||||||
| chr4:140648977
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0176others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+8120A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648977 | ||||||
| chr4:140649165
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(86): Show | 89 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.2337+7932G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649165 | ||||||
| chr4:140649167
|
G | A | 11 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0270others(8): Show | 11 | HG01261.hp2 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2337+7930C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649167 | ||||||
| chr4:140649276
|
T | C | 1 | a0001c0010t0001g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2337+7821A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649276 | ||||||
| chr4:140649368
|
G | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0176others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+7729C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649368 | ||||||
| chr4:140649518
|
A | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2337+7579T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649518 | ||||||
| chr4:140649540
|
C | A | 2 | a0001c0001t0004g0293a0001c0001t0016g0295 | 2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2337+7557G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649540 | ||||||
| chr4:140649549
|
T | C | 3 | a0001c0001t0001g0201a0001c0001t0001g0217a0001c0002t0001g0064 | 3 | HG02523.hp2 NA18941.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2337+7548A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649549 | ||||||
| chr4:140649552
|
A | T | 22 | a0001c0001t0001g0161a0001c0001t0001g0266a0001c0001t0002g0089others(19): Show | 22 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2337+7545T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649552 | ||||||
| chr4:140649563
|
A | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(46): Show | 49 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.2337+7534T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649563 | ||||||
| chr4:140649630
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2337+7467G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649630 | ||||||
| chr4:140649659
|
G | A | 33 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0002g0038others(30): Show | 33 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2337+7438C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649659 | ||||||
| chr4:140649743
|
C | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.2337+7354G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649743 | ||||||
| chr4:140649823
|
A | G | 1 | a0001c0005t0001g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2337+7274T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649823 | ||||||
| chr4:140649868
|
C | T | 7 | a0001c0001t0001g0167a0001c0002t0001g0050a0001c0002t0001g0188others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2337+7229G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649868 | ||||||
| chr4:140650042
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2337+7055T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650042 | ||||||
| chr4:140650060
|
T | C | 1 | a0001c0002t0001g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2337+7037A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650060 | ||||||
| chr4:140650603
|
G | C | 1 | a0001c0001t0001g0007 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2337+6494C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650603 | ||||||
| chr4:140650746
|
G | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0072others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2337+6351C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650746 | ||||||
| chr4:140650911
|
T | C | 1 | a0001c0004t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2337+6186A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650911 | ||||||
| chr4:140651522
|
G | A | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0002t0001g0100others(3): Show | 6 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2337+5575C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651522 | ||||||
| chr4:140651522
|
GGGTGA | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0023others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2337+5570_2337+557 others(9): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651522 | ||||||
| chr4:140651600
|
G | A | 1 | a0001c0003t0001g0021 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2337+5497C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651600 | ||||||
| chr4:140651628
|
G | A | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+5469C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651628 | ||||||
| chr4:140651639
|
T | C | 5 | a0001c0001t0001g0011a0001c0002t0001g0223a0001c0006t0001g0029others(2): Show | 5 | HG00423.hp1 NA18948.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+5458A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651639 | ||||||
| chr4:140651860
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2337+5237C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651860 | ||||||
| chr4:140651976
|
A | T | 254 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2337+5121T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651976 | ||||||
| chr4:140652159
|
T | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0001t0001g0140others(16): Show | 19 | HG01106.hp2 HG01261.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2337+4938A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652159 | ||||||
| chr4:140652195
|
C | T | 5 | a0001c0001t0001g0011a0001c0002t0001g0223a0001c0006t0001g0029others(2): Show | 5 | HG00423.hp1 NA18948.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+4902G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652195 | ||||||
| chr4:140652244
|
T | TA | 8 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0163others(5): Show | 8 | HG01106.hp2 HG01192.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+4852dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652244 | ||||||
| chr4:140652244
|
TA | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0090others(11): Show | 14 | HG01169.hp1 HG01257.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2337+4852delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652244 | ||||||
| chr4:140652412
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0002g0182 | 3 | HG02717.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2337+4685T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652412 | ||||||
| chr4:140652586
|
G | T | 12 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0002t0001g0100others(9): Show | 12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2337+4511C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652586 | ||||||
| chr4:140652588
|
A | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2337+4509T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652588 | ||||||
| chr4:140652919
|
C | T | 1 | a0001c0001t0004g0294 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2337+4178G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652919 | ||||||
| chr4:140652951
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2337+4146G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652951 | ||||||
| chr4:140653004
|
G | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2337+4093C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653004 | ||||||
| chr4:140653069
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2337+4028G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653069 | ||||||
| chr4:140653086
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 43 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2337+4011C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653086 | ||||||
| chr4:140653160
|
ATGAG | A | 11 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0270others(8): Show | 11 | HG01261.hp2 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2337+3933_2337+393 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653160 | ||||||
| chr4:140653229
|
C | T | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2337+3868G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653229 | ||||||
| chr4:140653265
|
T | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0166a0001c0001t0001g0198others(10): Show | 13 | HG01074.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.2337+3832A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653265 | ||||||
| chr4:140653269
|
T | C | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2337+3828A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653269 | ||||||
| chr4:140653389
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2337+3708G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653389 | ||||||
| chr4:140653459
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2337+3638C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653459 | ||||||
| chr4:140653514
|
T | C | 14 | a0001c0001t0001g0161a0001c0001t0002g0269a0001c0001t0003g0287others(11): Show | 14 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2337+3583A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653514 | ||||||
| chr4:140653660
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2337+3437C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653660 | ||||||
| chr4:140653895
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2337+3202G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653895 | ||||||
| chr4:140654168
|
G | A | 1 | a0001c0003t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2337+2929C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654168 | ||||||
| chr4:140654192
|
T | C | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+2905A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654192 | ||||||
| chr4:140654241
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG01243.hp2 HG01358.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2337+2856G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654241 | ||||||
| chr4:140654397
|
T | C | 3 | a0001c0002t0001g0267a0001c0002t0001g0268a0001c0004t0001g0086 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2337+2700A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654397 | ||||||
| chr4:140654441
|
A | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2337+2656T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654441 | ||||||
| chr4:140654448
|
A | G | 3 | a0001c0002t0001g0267a0001c0002t0001g0268a0001c0004t0001g0086 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2337+2649T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654448 | ||||||
| chr4:140654474
|
T | TG | 86 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(83): Show | 86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2337+2622dupC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654474 | ||||||
| chr4:140654474
|
TG | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(52): Show | 55 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2337+2622delC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654474 | ||||||
| chr4:140654487
|
T | C | 47 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(44): Show | 47 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2337+2610A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654487 | ||||||
| chr4:140654718
|
C | T | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2337+2379G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654718 | ||||||
| chr4:140654836
|
A | T | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+2261T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654836 | ||||||
| chr4:140654900
|
C | T | 7 | a0001c0001t0001g0140a0001c0001t0017g0297a0001c0002t0001g0244others(4): Show | 7 | HG01261.hp2 HG02258.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2337+2197G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654900 | ||||||
| chr4:140654941
|
A | G | 1 | a0001c0001t0003g0289 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2337+2156T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654941 | ||||||
| chr4:140654996
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2337+2101A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654996 | ||||||
| chr4:140655368
|
AT | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(30): Show | 33 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2337+1728delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655368 | ||||||
| chr4:140655425
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2337+1672T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655425 | ||||||
| chr4:140655519
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(88): Show | 91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2337+1578C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655519 | ||||||
| chr4:140655521
|
T | G | 2 | a0001c0002t0001g0211a0001c0002t0001g0222 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2337+1576A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655521 | ||||||
| chr4:140655530
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2337+1567A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655530 | ||||||
| chr4:140655605
|
T | C | 2 | a0001c0001t0001g0163a0001c0004t0001g0272 | 2 | HG01192.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2337+1492A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655605 | ||||||
| chr4:140655675
|
C | T | 2 | a0001c0005t0001g0159a0001c0005t0009g0004 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2337+1422G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655675 | ||||||
| chr4:140655750
|
A | G | 20 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(17): Show | 20 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.2337+1347T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655750 | ||||||
| chr4:140655955
|
A | T | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2337+1142T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655955 | ||||||
| chr4:140656081
|
A | G | 1 | a0001c0003t0007g0012 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2337+1016T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656081 | ||||||
| chr4:140656181
|
T | G | 1 | a0001c0008t0001g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2337+916A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656181 | ||||||
| chr4:140656209
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2337+888G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656209 | ||||||
| chr4:140656371
|
T | C | 1 | a0001c0003t0001g0021 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2337+726A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656371 | ||||||
| chr4:140656529
|
A | G | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2337+568T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656529 | ||||||
| chr4:140656622
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2337+475A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656622 | ||||||
| chr4:140656781
|
A | G | 2 | a0001c0004t0005g0265a0001c0013t0011g0115 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2337+316T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656781 | ||||||
| chr4:140656812
|
C | T | 2 | a0001c0001t0001g0166a0001c0002t0003g0283 | 2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2337+285G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656812 | ||||||
| chr4:140656817
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2337+280T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656817 | ||||||
| chr4:140656881
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2337+216C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656881 | ||||||
| chr4:140656933
|
A | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2337+164T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656933 | ||||||
| chr4:140656958
|
G | A | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(28): Show | 31 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2337+139C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656958 | ||||||
| chr4:140657001
|
C | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2337+96G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140657001 | ||||||
| chr4:140657492
|
G | A | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2207+35C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 12/20 | chr4 | 140657492 | ||||||
| chr4:140657957
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1922-145C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140657957 | ||||||
| chr4:140657993
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1922-181G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140657993 | ||||||
| chr4:140658035
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1922-223T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658035 | ||||||
| chr4:140658054
|
A | G | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1922-242T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658054 | ||||||
| chr4:140658097
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1922-285C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658097 | ||||||
| chr4:140658220
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1922-408C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658220 | ||||||
| chr4:140658247
|
A | C | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1922-435T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658247 | ||||||
| chr4:140658288
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1922-476T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658288 | ||||||
| chr4:140658300
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1922-488G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658300 | ||||||
| chr4:140658503
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1922-691G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658503 | ||||||
| chr4:140658541
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1922-729T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658541 | ||||||
| chr4:140658547
|
T | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0015others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1922-735A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658547 | ||||||
| chr4:140658571
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1922-759T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658571 | ||||||
| chr4:140658584
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0032others(32): Show | 35 | HG00099.hp1 HG00544.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1922-772G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658584 | ||||||
| chr4:140658681
|
G | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1922-869C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658681 | ||||||
| chr4:140658743
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1921+845C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658743 | ||||||
| chr4:140658767
|
C | G | 2 | a0001c0004t0001g0110a0001c0005t0001g0128 | 2 | HG02622.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1921+821G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658767 | ||||||
| chr4:140658808
|
TA | T | 9 | a0001c0001t0001g0079a0001c0003t0001g0041a0001c0003t0001g0042others(6): Show | 9 | HG00621.hp1 HG02723.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1921+779delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658808 | ||||||
| chr4:140659166
|
A | C | 1 | a0001c0001t0003g0289 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1921+422T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659166 | ||||||
| chr4:140659318
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1921+270G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659318 | ||||||
| chr4:140659407
|
C | T | 44 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0015others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1921+181G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659407 | ||||||
| chr4:140659549
|
C | T | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1921+39G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659549 | ||||||
| chr4:140659776
|
T | G | 1 | a0001c0003t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1804-71A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140659776 | ||||||
| chr4:140659880
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1804-175G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140659880 | ||||||
| chr4:140660052
|
C | T | 14 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1804-347G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660052 | ||||||
| chr4:140660227
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1804-522C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660227 | ||||||
| chr4:140660327
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1804-622G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660327 | ||||||
| chr4:140660424
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1804-719C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660424 | ||||||
| chr4:140660451
|
T | A | 1 | a0001c0010t0001g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1804-746A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660451 | ||||||
| chr4:140660573
|
G | C | 2 | a0001c0001t0001g0003a0001c0016t0012g0271 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1804-868C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660573 | ||||||
| chr4:140660607
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1804-902G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660607 | ||||||
| chr4:140660617
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1804-912A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660617 | ||||||
| chr4:140660671
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0003g0287others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1804-966C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660671 | ||||||
| chr4:140660676
|
G | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 183 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1804-971C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660676 | ||||||
| chr4:140660685
|
T | C | 2 | a0001c0004t0001g0142a0001c0021t0001g0264 | 2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1804-980A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660685 | ||||||
| chr4:140660822
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1803+1071G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660822 | ||||||
| chr4:140660833
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1803+1060C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660833 | ||||||
| chr4:140660886
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1803+1007C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660886 | ||||||
| chr4:140660917
|
C | CT | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1803+975dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660917 | ||||||
| chr4:140660917
|
C | CTT | 34 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0051others(31): Show | 34 | HG00639.hp1 HG01257.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1803+974_1803+975d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660917 | ||||||
| chr4:140660954
|
G | A | 4 | a0001c0005t0001g0129a0001c0005t0001g0171a0001c0005t0002g0127others(1): Show | 4 | HG00639.hp1 HG02300.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803+939C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660954 | ||||||
| chr4:140660960
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1803+933C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660960 | ||||||
| chr4:140660987
|
T | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1803+906A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660987 | ||||||
| chr4:140661035
|
C | T | 1 | a0001c0004t0002g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1803+858G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661035 | ||||||
| chr4:140661039
|
C | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1803+854G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661039 | ||||||
| chr4:140661063
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1803+830A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661063 | ||||||
| chr4:140661072
|
G | A | 1 | a0001c0003t0001g0068 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1803+821C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661072 | ||||||
| chr4:140661107
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1803+786A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661107 | ||||||
| chr4:140661108
|
G | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1803+785C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661108 | ||||||
| chr4:140661131
|
G | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0266a0001c0001t0001g0270others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803+762C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661131 | ||||||
| chr4:140661150
|
G | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803+743C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661150 | ||||||
| chr4:140661165
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1803+728A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661165 | ||||||
| chr4:140661214
|
G | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1803+679C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661214 | ||||||
| chr4:140661236
|
T | A | 8 | a0001c0005t0001g0145a0001c0005t0001g0157a0001c0008t0001g0179others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1803+657A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661236 | ||||||
| chr4:140661286
|
G | C | 35 | a0001c0001t0001g0063a0001c0001t0002g0243a0001c0003t0001g0008others(32): Show | 35 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1803+607C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661286 | ||||||
| chr4:140661346
|
T | C | 6 | a0001c0004t0001g0142a0001c0004t0005g0265a0001c0013t0011g0115others(3): Show | 6 | HG02559.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+547A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661346 | ||||||
| chr4:140661431
|
C | T | 6 | a0001c0001t0001g0011a0001c0002t0001g0223a0001c0003t0001g0253others(3): Show | 6 | HG00423.hp1 NA18948.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+462G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661431 | ||||||
| chr4:140661593
|
C | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1803+300G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661593 | ||||||
| chr4:140661690
|
G | T | 19 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(16): Show | 19 | HG00639.hp1 HG01361.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1803+203C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661690 | ||||||
| chr4:140661755
|
G | A | 1 | a0001c0001t0004g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1803+138C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661755 | ||||||
| chr4:140662385
|
C | T | 2 | a0001c0004t0001g0152a0001c0012t0008g0146 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1589-278G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662385 | ||||||
| chr4:140662673
|
T | C | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1589-566A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662673 | ||||||
| chr4:140662738
|
T | A | 37 | a0001c0001t0001g0063a0001c0003t0001g0008a0001c0004t0001g0045others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1589-631A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662738 | ||||||
| chr4:140662800
|
T | A | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1589-693A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662800 | ||||||
| chr4:140662801
|
A | G | 24 | a0001c0005t0001g0114a0001c0005t0001g0128a0001c0005t0001g0129others(21): Show | 24 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1589-694T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662801 | ||||||
| chr4:140662811
|
C | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1589-704G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662811 | ||||||
| chr4:140663028
|
C | T | 23 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-921G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663028 | ||||||
| chr4:140663484
|
G | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0002t0001g0094others(23): Show | 26 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1589-1377C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663484 | ||||||
| chr4:140663510
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1589-1403G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663510 | ||||||
| chr4:140663514
|
T | A | 17 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0140others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1589-1407A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663514 | ||||||
| chr4:140663603
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1589-1496C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663603 | ||||||
| chr4:140663882
|
T | C | 2 | a0001c0004t0001g0142a0001c0021t0001g0264 | 2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1589-1775A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663882 | ||||||
| chr4:140663912
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0139others(33): Show | 36 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1589-1805A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663912 | ||||||
| chr4:140663977
|
T | C | 23 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-1870A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663977 | ||||||
| chr4:140664039
|
C | CA | 5 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0165others(2): Show | 5 | HG02738.hp2 NA18981.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589-1933_1589-193 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664039 | ||||||
| chr4:140664040
|
C | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1589-1933G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664040 | ||||||
| chr4:140664040
|
C | CA | 24 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1589-1934dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664040 | ||||||
| chr4:140664209
|
C | T | 1 | a0001c0002t0015g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1589-2102G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664209 | ||||||
| chr4:140664215
|
C | A | 1 | a0001c0006t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1589-2108G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664215 | ||||||
| chr4:140664283
|
AC | A | 23 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-2177delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664283 | ||||||
| chr4:140664705
|
CA | C | 7 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1589-2599delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664705 | ||||||
| chr4:140664768
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0140others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1589-2661G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664768 | ||||||
| chr4:140664831
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1589-2724C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664831 | ||||||
| chr4:140664973
|
G | T | 23 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(20): Show | 23 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1589-2866C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664973 | ||||||
| chr4:140664989
|
C | A | 2 | a0001c0001t0001g0270a0001c0001t0002g0269 | 2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1589-2882G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664989 | ||||||
| chr4:140665022
|
G | T | 23 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(20): Show | 23 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1589-2915C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665022 | ||||||
| chr4:140665051
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1589-2944C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665051 | ||||||
| chr4:140665071
|
C | T | 47 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(44): Show | 47 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.1589-2964G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665071 | ||||||
| chr4:140665109
|
G | GA | 8 | a0001c0001t0004g0292a0001c0001t0010g0054a0001c0003t0001g0083others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1589-3003dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665109 | ||||||
| chr4:140665277
|
C | T | 1 | a0001c0006t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1589-3170G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665277 | ||||||
| chr4:140665368
|
G | A | 1 | a0001c0002t0002g0220 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1589-3261C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665368 | ||||||
| chr4:140665495
|
T | C | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1589-3388A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665495 | ||||||
| chr4:140665693
|
C | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1588+3224G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665693 | ||||||
| chr4:140665752
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1588+3165A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665752 | ||||||
| chr4:140665823
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1588+3094G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665823 | ||||||
| chr4:140666086
|
G | A | 37 | a0001c0001t0001g0063a0001c0003t0001g0008a0001c0004t0001g0045others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1588+2831C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666086 | ||||||
| chr4:140666088
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1588+2829T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666088 | ||||||
| chr4:140666095
|
G | A | 5 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1588+2822C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666095 | ||||||
| chr4:140666110
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1588+2807A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666110 | ||||||
| chr4:140666139
|
G | C | 47 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(44): Show | 47 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.1588+2778C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666139 | ||||||
| chr4:140666374
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0140others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1588+2543G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666374 | ||||||
| chr4:140666460
|
C | T | 1 | a0001c0004t0001g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1588+2457G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666460 | ||||||
| chr4:140666480
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0163 | 2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1588+2437G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666480 | ||||||
| chr4:140666523
|
A | T | 1 | a0002c0009t0002g0120 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1588+2394T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666523 | ||||||
| chr4:140666627
|
C | A | 23 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(20): Show | 23 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1588+2290G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666627 | ||||||
| chr4:140666629
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1588+2288G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666629 | ||||||
| chr4:140666734
|
T | TA | 36 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0002g0274others(33): Show | 36 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.1588+2182dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666734 | ||||||
| chr4:140666734
|
T | TAA | 37 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(34): Show | 37 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1588+2181_1588+218 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666734 | ||||||
| chr4:140666734
|
T | TAAAA | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1588+2179_1588+218 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666734 | ||||||
| chr4:140666743
|
A | G | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1588+2174T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666743 | ||||||
| chr4:140666821
|
G | GAT | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1588+2094_1588+209 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666821 | ||||||
| chr4:140666884
|
C | A | 23 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1588+2033G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666884 | ||||||
| chr4:140667160
|
G | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1588+1757C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667160 | ||||||
| chr4:140667287
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0251 | 2 | HG02738.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1588+1630C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667287 | ||||||
| chr4:140667315
|
T | A | 2 | a0001c0004t0005g0265a0001c0013t0011g0115 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1588+1602A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667315 | ||||||
| chr4:140667324
|
G | A | 1 | a0001c0004t0001g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1588+1593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667324 | ||||||
| chr4:140667349
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1588+1568G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667349 | ||||||
| chr4:140667461
|
C | G | 1 | a0001c0005t0001g0129 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1588+1456G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667461 | ||||||
| chr4:140667557
|
G | A | 3 | a0001c0004t0005g0265a0001c0013t0011g0115a0001c0020t0001g0187 | 3 | HG02886.hp1 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1588+1360C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667557 | ||||||
| chr4:140667653
|
C | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(17): Show | 20 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+1264G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667653 | ||||||
| chr4:140667939
|
C | T | 25 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(22): Show | 25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1588+978G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667939 | ||||||
| chr4:140667959
|
T | C | 26 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(23): Show | 26 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1588+958A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667959 | ||||||
| chr4:140667990
|
A | G | 1 | a0001c0014t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1588+927T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667990 | ||||||
| chr4:140668110
|
G | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(17): Show | 20 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+807C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668110 | ||||||
| chr4:140668147
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(185): Show | 188 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1588+770C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668147 | ||||||
| chr4:140668168
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(17): Show | 20 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+749C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668168 | ||||||
| chr4:140668225
|
T | C | 22 | a0001c0004t0001g0142a0001c0005t0001g0114a0001c0005t0001g0128others(19): Show | 22 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1588+692A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668225 | ||||||
| chr4:140668509
|
A | G | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1588+408T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668509 | ||||||
| chr4:140668527
|
T | C | 1 | a0001c0005t0001g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1588+390A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668527 | ||||||
| chr4:140668532
|
T | G | 3 | a0001c0004t0005g0265a0001c0013t0011g0115a0001c0020t0001g0187 | 3 | HG02886.hp1 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1588+385A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668532 | ||||||
| chr4:140668552
|
A | T | 1 | a0001c0002t0001g0094 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1588+365T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668552 | ||||||
| chr4:140668888
|
C | T | 2 | a0001c0001t0001g0058a0001c0007t0001g0229 | 2 | HG03710.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1588+29G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668888 | ||||||
| chr4:140668889
|
G | A | 11 | a0001c0002t0001g0050a0001c0002t0001g0188a0001c0002t0001g0196others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588+28C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668889 | ||||||
| chr4:140669087
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1438-20T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 8/20 | chr4 | 140669087 | ||||||
| chr4:140669160
|
C | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438-93G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 8/20 | chr4 | 140669160 | ||||||
| chr4:140669332
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1438-265G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 8/20 | chr4 | 140669332 | ||||||
| chr4:140669937
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1267-133G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140669937 | ||||||
| chr4:140670322
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1266+398T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670322 | ||||||
| chr4:140670557
|
C | T | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1266+163G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670557 | ||||||
| chr4:140670615
|
G | A | 12 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(9): Show | 12 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.1266+105C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670615 | ||||||
| chr4:140670704
|
G | T | 1 | a0001c0004t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1266+16C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670704 | ||||||
| chr4:140670972
|
C | G | 2 | a0001c0001t0014g0284a0001c0003t0003g0285 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-46G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140670972 | ||||||
| chr4:140671052
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1060-126T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671052 | ||||||
| chr4:140671071
|
G | C | 2 | a0001c0003t0001g0083a0001c0015t0002g0084 | 2 | NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1060-145C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671071 | ||||||
| chr4:140671139
|
G | A | 2 | a0001c0004t0005g0265a0001c0013t0011g0115 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1060-213C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671139 | ||||||
| chr4:140671219
|
T | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1060-293A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671219 | ||||||
| chr4:140671416
|
A | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1060-490T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671416 | ||||||
| chr4:140671550
|
T | C | 2 | a0001c0005t0001g0159a0001c0005t0009g0004 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1060-624A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671550 | ||||||
| chr4:140671669
|
C | T | 1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060-743G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671669 | ||||||
| chr4:140671674
|
C | CTG | 42 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0032others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1060-750_1060-749d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTG | 16 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0049others(13): Show | 16 | HG01175.hp2 HG01255.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-752_1060-749d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTG | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0002g0274others(2): Show | 5 | HG02965.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-754_1060-749d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0035a0001c0001t0001g0237a0001c0001t0002g0156others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-756_1060-749d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(3): Show |
1 | a0001c0008t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1060-758_1060-749d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(5): Show |
11 | a0001c0001t0001g0138a0001c0002t0001g0267a0001c0002t0001g0268others(8): Show | 11 | HG02451.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1060-760_1060-749d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(7): Show |
4 | a0001c0001t0001g0090a0001c0001t0001g0147a0001c0001t0001g0149others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-762_1060-749d others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(9): Show |
7 | a0001c0001t0001g0093a0001c0001t0001g0148a0001c0001t0001g0153others(4): Show | 7 | HG01192.hp1 HG02717.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-764_1060-749d others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(11): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0092a0001c0001t0001g0144others(3): Show | 6 | HG02280.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-766_1060-749d others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-768_1060-749d others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
CTG | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1060-750_1060-749d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
CTGTG | C | 4 | a0001c0004t0001g0142a0001c0004t0001g0168a0001c0005t0001g0114others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-752_1060-749d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
CTGTGTG | C | 4 | a0001c0004t0005g0265a0001c0007t0007g0106a0001c0013t0011g0115others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-754_1060-749d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
CTGTGTGT others(1): Show |
C | 44 | a0001c0004t0001g0045a0001c0004t0001g0103a0001c0004t0001g0107others(41): Show | 44 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1060-756_1060-749d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671674
|
CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0001g0002a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG03209.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-758_1060-749d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | ||||||
| chr4:140671712
|
G | GTGTA | 3 | a0001c0001t0001g0176a0001c0001t0001g0266a0001c0001t0006g0141 | 3 | HG02055.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671712
|
G | GTGTGTGT others(1): Show |
4 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0002t0001g0244others(1): Show | 4 | HG01106.hp2 HG02258.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-787_1060-786i others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671712
|
G | GTGTGTGT others(3): Show |
1 | a0001c0003t0003g0285 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1060-787_1060-786i others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671712
|
G | GTGTGTGT others(5): Show |
3 | a0001c0001t0014g0284a0001c0004t0001g0228a0001c0004t0002g0260 | 3 | HG02723.hp1 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671712
|
G | GTGTGTGT others(7): Show |
3 | a0001c0001t0001g0270a0001c0001t0002g0269a0001c0001t0017g0297 | 3 | HG02258.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671712
|
G | GTGTGTGT others(9): Show |
3 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0016t0012g0271 | 3 | HG01070.hp2 HG01071.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671712
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0161 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1060-787_1060-786i others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | ||||||
| chr4:140671902
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1060-976A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671902 | ||||||
| chr4:140671987
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-1061A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671987 | ||||||
| chr4:140672078
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1060-1152A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672078 | ||||||
| chr4:140672159
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1060-1233C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672159 | ||||||
| chr4:140672198
|
A | G | 15 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(12): Show | 15 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-1272T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672198 | ||||||
| chr4:140672349
|
T | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 187 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1060-1423A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672349 | ||||||
| chr4:140672468
|
T | G | 2 | a0001c0005t0001g0159a0001c0005t0009g0004 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1060-1542A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672468 | ||||||
| chr4:140672483
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1060-1557C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672483 | ||||||
| chr4:140672561
|
T | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1060-1635A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672561 | ||||||
| chr4:140672709
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1060-1783T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672709 | ||||||
| chr4:140672721
|
C | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(16): Show | 19 | HG00544.hp1 HG00558.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1060-1795G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672721 | ||||||
| chr4:140672862
|
T | A | 1 | a0001c0001t0002g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1060-1936A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672862 | ||||||
| chr4:140672869
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1060-1943A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672869 | ||||||
| chr4:140672890
|
T | C | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1060-1964A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672890 | ||||||
| chr4:140672926
|
T | A | 20 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0160others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-2000A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672926 | ||||||
| chr4:140673167
|
C | CA | 7 | a0001c0001t0001g0161a0001c0001t0001g0270a0001c0001t0002g0269others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-2242dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673167 | ||||||
| chr4:140673167
|
CA | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1060-2242delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673167 | ||||||
| chr4:140673185
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-2259A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673185 | ||||||
| chr4:140673265
|
G | C | 1 | a0001c0008t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1060-2339C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673265 | ||||||
| chr4:140673304
|
C | A | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-2378G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673304 | ||||||
| chr4:140673486
|
A | C | 1 | a0001c0002t0001g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1060-2560T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673486 | ||||||
| chr4:140673499
|
G | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 272 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.1060-2573C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673499 | ||||||
| chr4:140673598
|
A | G | 3 | a0001c0004t0001g0086a0001c0004t0005g0265a0001c0013t0011g0115 | 3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1060-2672T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673598 | ||||||
| chr4:140673751
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1060-2825T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673751 | ||||||
| chr4:140673949
|
T | C | 39 | a0001c0004t0001g0045a0001c0004t0001g0086a0001c0004t0001g0103others(36): Show | 39 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1059+2945A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673949 | ||||||
| chr4:140674170
|
G | C | 3 | a0001c0002t0001g0206a0001c0002t0001g0214a0001c0002t0001g0234 | 3 | HG00609.hp2 HG00673.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1059+2724C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674170 | ||||||
| chr4:140674279
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1059+2615A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674279 | ||||||
| chr4:140674333
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1059+2561A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674333 | ||||||
| chr4:140674353
|
C | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+2541G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674353 | ||||||
| chr4:140674529
|
T | G | 3 | a0001c0001t0001g0081a0001c0003t0001g0083a0001c0015t0002g0084 | 3 | NA18941.hp1 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1059+2365A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674529 | ||||||
| chr4:140674597
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+2297A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674597 | ||||||
| chr4:140674676
|
A | AAT | 39 | a0001c0001t0001g0002a0001c0004t0001g0045a0001c0004t0001g0086others(36): Show | 39 | HG00408.hp2 HG00558.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059+2216_1059+221 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674676 | ||||||
| chr4:140674676
|
A | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+2218T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674676 | ||||||
| chr4:140674687
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1059+2207T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674687 | ||||||
| chr4:140674691
|
A | AT | 9 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(6): Show | 9 | HG01361.hp2 HG02300.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+2202dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674691 | ||||||
| chr4:140674691
|
A | T | 15 | a0001c0001t0001g0011a0001c0002t0001g0097a0001c0002t0001g0098others(12): Show | 15 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+2203T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674691 | ||||||
| chr4:140674692
|
T | TA | 18 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(15): Show | 18 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1059+2201_1059+220 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674692 | ||||||
| chr4:140674693
|
T | A | 42 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0049others(39): Show | 42 | HG00639.hp2 HG01074.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1059+2201A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674693 | ||||||
| chr4:140674694
|
T | A | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1059+2200A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674694 | ||||||
| chr4:140674704
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(67): Show | 70 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1059+2190A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674704 | ||||||
| chr4:140674791
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+2103A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674791 | ||||||
| chr4:140674836
|
C | T | 31 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(28): Show | 31 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059+2058G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674836 | ||||||
| chr4:140674862
|
C | T | 3 | a0001c0004t0001g0086a0001c0004t0005g0265a0001c0013t0011g0115 | 3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1059+2032G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674862 | ||||||
| chr4:140674868
|
T | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1059+2026A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674868 | ||||||
| chr4:140674960
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+1934G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674960 | ||||||
| chr4:140674994
|
C | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1059+1900G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674994 | ||||||
| chr4:140675008
|
C | A | 2 | a0001c0005t0001g0159a0001c0005t0009g0004 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1059+1886G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675008 | ||||||
| chr4:140675210
|
G | A | 2 | a0001c0008t0001g0240a0001c0008t0005g0241 | 2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1059+1684C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675210 | ||||||
| chr4:140675234
|
A | AC | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(221): Show | 224 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1059+1659_1059+166 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675234 | ||||||
| chr4:140675498
|
C | A | 5 | a0001c0002t0001g0100a0001c0002t0001g0104a0001c0002t0006g0099others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+1396G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675498 | ||||||
| chr4:140675537
|
G | C | 1 | a0001c0002t0001g0207 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1059+1357C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675537 | ||||||
| chr4:140675563
|
T | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0072a0001c0001t0001g0191others(4): Show | 7 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+1331A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675563 | ||||||
| chr4:140675616
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1059+1278A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675616 | ||||||
| chr4:140675631
|
T | G | 25 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1059+1263A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675631 | ||||||
| chr4:140675836
|
C | A | 33 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(30): Show | 33 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1059+1058G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675836 | ||||||
| chr4:140676241
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1059+653C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676241 | ||||||
| chr4:140676259
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1059+635G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676259 | ||||||
| chr4:140676267
|
G | A | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+627C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676267 | ||||||
| chr4:140676626
|
G | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1059+268C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676626 | ||||||
| chr4:140676733
|
T | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0237a0001c0001t0002g0156others(1): Show | 4 | HG02055.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+161A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676733 | ||||||
| chr4:140676759
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1059+135T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676759 | ||||||
| chr4:140677136
|
A | G | 41 | a0001c0004t0001g0045a0001c0004t0001g0086a0001c0004t0001g0103others(38): Show | 41 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.852-35T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677136 | ||||||
| chr4:140677168
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(23): Show | 26 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.852-67C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677168 | ||||||
| chr4:140677407
|
A | G | 41 | a0001c0004t0001g0045a0001c0004t0001g0086a0001c0004t0001g0103others(38): Show | 41 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.852-306T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677407 | ||||||
| chr4:140677645
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.852-544A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677645 | ||||||
| chr4:140677693
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.852-592G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677693 | ||||||
| chr4:140677707
|
C | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0222 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.852-606G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677707 | ||||||
| chr4:140677771
|
C | T | 2 | a0001c0002t0001g0244a0001c0021t0001g0264 | 2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.852-670G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677771 | ||||||
| chr4:140677874
|
T | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-773A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677874 | ||||||
| chr4:140677882
|
C | T | 2 | a0001c0005t0001g0159a0001c0005t0009g0004 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.852-781G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677882 | ||||||
| chr4:140678018
|
T | TA | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.852-918dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678018 | ||||||
| chr4:140678206
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.851+736A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678206 | ||||||
| chr4:140678285
|
T | C | 34 | a0001c0004t0001g0045a0001c0004t0001g0103a0001c0004t0001g0107others(31): Show | 34 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.851+657A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678285 | ||||||
| chr4:140678324
|
C | T | 15 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 15 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.851+618G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678324 | ||||||
| chr4:140678533
|
G | T | 1 | a0001c0008t0005g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.851+409C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678533 | ||||||
| chr4:140678544
|
C | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.851+398G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678544 | ||||||
| chr4:140678687
|
T | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.851+255A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678687 | ||||||
| chr4:140678859
|
G | A | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.851+83C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678859 | ||||||
| chr4:140679218
|
C | T | 2 | a0001c0001t0003g0287a0001c0001t0003g0288 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.590-15G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/20 | chr4 | 140679218 | ||||||
| chr4:140679390
|
T | C | 31 | a0001c0004t0001g0045a0001c0004t0001g0103a0001c0004t0001g0107others(28): Show | 31 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.590-187A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/20 | chr4 | 140679390 | ||||||
| chr4:140679486
|
T | TA | 26 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(23): Show | 26 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.589+128dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/20 | chr4 | 140679486 | ||||||
| chr4:140679935
|
T | TA | 122 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.361-93dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140679935 | ||||||
| chr4:140680035
|
A | G | 1 | a0001c0004t0001g0272 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.361-192T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680035 | ||||||
| chr4:140680266
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.361-423G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680266 | ||||||
| chr4:140680440
|
G | A | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-597C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680440 | ||||||
| chr4:140680530
|
G | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-687C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680530 | ||||||
| chr4:140680538
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-695T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680538 | ||||||
| chr4:140680603
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0191 | 2 | HG00544.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.361-760G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680603 | ||||||
| chr4:140680768
|
T | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.361-925A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680768 | ||||||
| chr4:140680859
|
G | A | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.361-1016C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680859 | ||||||
| chr4:140680900
|
T | C | 1 | a0001c0002t0001g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.361-1057A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680900 | ||||||
| chr4:140681342
|
A | G | 1 | a0001c0002t0002g0091 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.361-1499T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681342 | ||||||
| chr4:140681520
|
A | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-1677T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681520 | ||||||
| chr4:140681529
|
A | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(43): Show | 46 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.361-1686T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681529 | ||||||
| chr4:140681575
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.361-1732G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681575 | ||||||
| chr4:140681904
|
A | G | 25 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(22): Show | 25 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.361-2061T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681904 | ||||||
| chr4:140681920
|
C | G | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.361-2077G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681920 | ||||||
| chr4:140682165
|
A | G | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-2322T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682165 | ||||||
| chr4:140682203
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.361-2360A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682203 | ||||||
| chr4:140682315
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 272 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.361-2472A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682315 | ||||||
| chr4:140682342
|
G | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.361-2499C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682342 | ||||||
| chr4:140682515
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.361-2672C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682515 | ||||||
| chr4:140682823
|
A | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.361-2980T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682823 | ||||||
| chr4:140682949
|
C | T | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-3106G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682949 | ||||||
| chr4:140683044
|
G | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.361-3201C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683044 | ||||||
| chr4:140683167
|
C | T | 1 | a0001c0004t0005g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.360+3177G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683167 | ||||||
| chr4:140683404
|
T | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+2940A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683404 | ||||||
| chr4:140683418
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.360+2926G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683418 | ||||||
| chr4:140683431
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+2913A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683431 | ||||||
| chr4:140683492
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.360+2852C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683492 | ||||||
| chr4:140683725
|
T | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.360+2619A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683725 | ||||||
| chr4:140683798
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.360+2546A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683798 | ||||||
| chr4:140683802
|
G | A | 6 | a0001c0001t0001g0161a0001c0001t0001g0270a0001c0001t0002g0269others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+2542C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683802 | ||||||
| chr4:140684240
|
TA | T | 64 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(61): Show | 64 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.360+2103delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684240 | ||||||
| chr4:140684323
|
A | G | 25 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(22): Show | 25 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.360+2021T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684323 | ||||||
| chr4:140684554
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.360+1790A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684554 | ||||||
| chr4:140684570
|
T | C | 2 | a0001c0005t0002g0101a0001c0005t0002g0102 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.360+1774A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684570 | ||||||
| chr4:140684712
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.360+1632T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684712 | ||||||
| chr4:140684733
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.360+1611C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684733 | ||||||
| chr4:140684872
|
AG | A | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.360+1471delC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684872 | ||||||
| chr4:140685130
|
C | G | 1 | a0003c0019t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.360+1214G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685130 | ||||||
| chr4:140685149
|
A | G | 1 | a0001c0004t0001g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.360+1195T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685149 | ||||||
| chr4:140685175
|
C | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.360+1169G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685175 | ||||||
| chr4:140685218
|
T | C | 2 | a0001c0008t0001g0240a0001c0008t0005g0241 | 2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.360+1126A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685218 | ||||||
| chr4:140685431
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+913G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685431 | ||||||
| chr4:140685432
|
G | A | 36 | a0001c0004t0001g0045a0001c0004t0001g0103a0001c0004t0001g0107others(33): Show | 36 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.360+912C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685432 | ||||||
| chr4:140685530
|
C | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.360+814G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685530 | ||||||
| chr4:140685805
|
T | A | 4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0180others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+539A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685805 | ||||||
| chr4:140685914
|
C | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+430G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685914 | ||||||
| chr4:140685938
|
TAAC | T | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.360+403_360+405del others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685938 | ||||||
| chr4:140686098
|
A | G | 1 | a0001c0002t0001g0202 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.360+246T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140686098 | ||||||
| chr4:140686256
|
G | C | 5 | a0001c0004t0001g0086a0001c0004t0001g0228a0001c0004t0002g0260others(2): Show | 5 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+88C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140686256 | ||||||
| chr4:140686525
|
C | T | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.242-63G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686525 | ||||||
| chr4:140686603
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-141G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686603 | ||||||
| chr4:140686628
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-166A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686628 | ||||||
| chr4:140686644
|
C | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0073 | 2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.242-182G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686644 | ||||||
| chr4:140686645
|
G | A | 2 | a0001c0008t0001g0240a0001c0008t0005g0241 | 2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.242-183C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686645 | ||||||
| chr4:140686822
|
G | C | 1 | a0001c0008t0005g0241 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.242-360C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686822 | ||||||
| chr4:140687153
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.242-691T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687153 | ||||||
| chr4:140687242
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-780T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687242 | ||||||
| chr4:140687321
|
A | ATATG | 5 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0167others(2): Show | 5 | HG00423.hp2 HG00544.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-860_242-859ins others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | ||||||
| chr4:140687321
|
A | ATATGTG | 74 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.242-860_242-859ins others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | ||||||
| chr4:140687321
|
A | ATGTGTG | 3 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0003g0278 | 3 | HG01975.hp1 HG01978.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.242-865_242-860dup others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | ||||||
| chr4:140687321
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.242-859T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | ||||||
| chr4:140687323
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0033others(16): Show | 19 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.242-861C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687323 | ||||||
| chr4:140687338
|
TGTGTCAT others(31): Show |
T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-914_242-877del others(38): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687338 | ||||||
| chr4:140687341
|
GTCA | G | 25 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0090others(22): Show | 25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.242-882_242-880del others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | ||||||
| chr4:140687341
|
GTCATA | G | 9 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0002g0066others(6): Show | 9 | HG02738.hp2 HG04199.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-884_242-880del others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | ||||||
| chr4:140687341
|
GTCATATA | G | 37 | a0001c0001t0001g0140a0001c0001t0001g0163a0001c0001t0002g0089others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.242-886_242-880del others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | ||||||
| chr4:140687341
|
GTCATATA others(18): Show |
G | 2 | a0001c0001t0001g0006a0001c0001t0001g0062 | 2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.242-904_242-880del others(25): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | ||||||
| chr4:140687342
|
T | TGTCATAT others(3): Show |
1 | a0001c0001t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.242-881_242-880ins others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(5): Show |
1 | a0001c0001t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(7): Show |
3 | a0001c0001t0001g0208a0001c0001t0003g0279a0001c0001t0004g0296 | 3 | HG03834.hp2 NA18963.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.242-881_242-880ins others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(9): Show |
1 | a0001c0001t0016g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(11): Show |
1 | a0001c0001t0004g0294 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.242-881_242-880ins others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(15): Show |
1 | a0001c0001t0004g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.242-881_242-880ins others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(17): Show |
1 | a0001c0001t0001g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(19): Show |
1 | a0001c0001t0001g0194 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(26): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(25): Show |
2 | a0001c0001t0003g0289a0001c0001t0004g0291 | 2 | NA19012.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.242-881_242-880ins others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTC others(27): Show |
1 | a0001c0003t0001g0071 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(34): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
TC | T | 9 | a0001c0001t0001g0203a0001c0001t0001g0212a0001c0001t0002g0156others(6): Show | 9 | HG00621.hp1 HG00642.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.242-881delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687342
|
TCATATAT others(3): Show |
T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-890_242-881del others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | ||||||
| chr4:140687343
|
C | CAT | 19 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0027others(16): Show | 20 | HG00099.hp2 HG00423.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.242-883_242-882dup others(2): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | CATAT | 21 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0056others(18): Show | 21 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.242-885_242-882dup others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | CATATAT | 18 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0028others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.242-887_242-882dup others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | CATATATA others(1): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0076a0001c0001t0001g0108others(2): Show | 5 | HG00673.hp2 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-889_242-882dup others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | CATATATA others(3): Show |
9 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0217others(6): Show | 9 | HG00140.hp2 HG01496.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-891_242-882dup others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | CATATATA others(7): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0256others(1): Show | 4 | HG01928.hp1 NA18972.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-895_242-882dup others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | CATATATA others(9): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01346.hp1 HG02004.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-897_242-882dup others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0112others(2): Show | 5 | HG00423.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-881G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
C | T | 18 | a0001c0001t0001g0051a0001c0001t0001g0194a0001c0001t0001g0208others(15): Show | 18 | HG01257.hp1 HG01261.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-881G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CAT | C | 11 | a0001c0002t0001g0173a0001c0002t0001g0195a0001c0002t0001g0202others(8): Show | 11 | HG01069.hp2 HG01123.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.242-883_242-882del others(2): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATAT | C | 7 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0002t0001g0242others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.242-885_242-882del others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATAT | C | 8 | a0001c0002t0001g0050a0001c0002t0001g0180a0001c0002t0001g0192others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-887_242-882del others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(1): Show |
C | 11 | a0001c0001t0014g0284a0001c0002t0001g0097a0001c0002t0001g0098others(8): Show | 11 | HG00639.hp2 HG00673.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-889_242-882del others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(3): Show |
C | 6 | a0001c0002t0001g0214a0001c0002t0001g0223a0001c0002t0001g0267others(3): Show | 6 | HG00609.hp2 HG01081.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-891_242-882del others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(5): Show |
C | 4 | a0001c0002t0001g0100a0001c0002t0006g0164a0001c0003t0003g0285others(1): Show | 4 | HG00735.hp1 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-893_242-882del others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(7): Show |
C | 2 | a0001c0002t0001g0104a0001c0002t0006g0099 | 2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.242-895_242-882del others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(9): Show |
C | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0006g0141others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-897_242-882del others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0160a0001c0002t0003g0290a0001c0016t0012g0271 | 3 | HG02559.hp1 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.242-899_242-882del others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(13): Show |
C | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.242-901_242-882del others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(15): Show |
C | 8 | a0001c0001t0001g0161a0001c0001t0001g0270a0001c0001t0002g0269others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-903_242-882del others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687343
|
CATATATA others(17): Show |
C | 8 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0133others(5): Show | 8 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-905_242-882del others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | ||||||
| chr4:140687344
|
A | G | 10 | a0001c0001t0001g0203a0001c0001t0001g0212a0001c0001t0002g0156others(7): Show | 10 | HG00621.hp1 HG00642.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-882T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687344 | ||||||
| chr4:140687344
|
A | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0112others(2): Show | 5 | HG00423.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-882T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687344 | ||||||
| chr4:140687345
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0112others(2): Show | 5 | HG00423.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-883A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687345 | ||||||
| chr4:140687346
|
A | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0090others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.242-884T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687346 | ||||||
| chr4:140687348
|
A | G | 43 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0090others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.242-886T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687348 | ||||||
| chr4:140687349
|
T | G | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.242-887A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687349 | ||||||
| chr4:140687349
|
T | TC | 7 | a0001c0001t0001g0212a0001c0003t0001g0041a0001c0003t0001g0055others(4): Show | 7 | HG00621.hp1 HG00642.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.242-888_242-887ins others(1): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687349 | ||||||
| chr4:140687350
|
A | G | 72 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0090others(69): Show | 72 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.242-888T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687350 | ||||||
| chr4:140687350
|
A | T | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.242-888T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687350 | ||||||
| chr4:140687351
|
T | C | 2 | a0001c0001t0001g0203a0001c0008t0001g0240 | 2 | NA18970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.242-889A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687351 | ||||||
| chr4:140687351
|
TA | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0018t0001g0174 | 3 | HG03710.hp2 NA19011.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.242-890delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687351 | ||||||
| chr4:140687351
|
TATATATA others(38): Show |
T | 1 | a0001c0003t0001g0008 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.242-934_242-890del others(45): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687351 | ||||||
| chr4:140687352
|
A | G | 70 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(67): Show | 70 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.242-890T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687352 | ||||||
| chr4:140687353
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0018t0001g0174 | 3 | HG03710.hp2 NA19011.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.242-891A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687353 | ||||||
| chr4:140687353
|
T | G | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-891A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687353 | ||||||
| chr4:140687353
|
TA | T | 68 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(65): Show | 68 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.242-892delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687353 | ||||||
| chr4:140687354
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.242-892T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687354 | ||||||
| chr4:140687354
|
A | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-892T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687354 | ||||||
| chr4:140687355
|
T | C | 69 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(66): Show | 69 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.242-893A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687355 | ||||||
| chr4:140687356
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.242-894T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687356 | ||||||
| chr4:140687358
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.242-896T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687358 | ||||||
| chr4:140687360
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.242-898T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687360 | ||||||
| chr4:140687361
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.242-899A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687361 | ||||||
| chr4:140687363
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.242-901A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687363 | ||||||
| chr4:140687368
|
A | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0090others(65): Show | 68 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.242-906T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687368 | ||||||
| chr4:140687370
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0062 | 2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.242-908T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687370 | ||||||
| chr4:140687370
|
A | T | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-908T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687370 | ||||||
| chr4:140687372
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0062 | 2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.242-910T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687372 | ||||||
| chr4:140687377
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-915A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687377 | ||||||
| chr4:140687378
|
A | G | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-916T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687378 | ||||||
| chr4:140687380
|
A | T | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-918T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687380 | ||||||
| chr4:140687388
|
A | G | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-926T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687388 | ||||||
| chr4:140687389
|
T | A | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-927A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687389 | ||||||
| chr4:140687390
|
A | C | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-928T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687390 | ||||||
| chr4:140687396
|
A | AT | 3 | a0001c0002t0001g0094a0001c0002t0001g0196a0001c0002t0001g0236 | 3 | HG01169.hp1 HG01169.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.242-935_242-934ins others(1): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687396 | ||||||
| chr4:140687396
|
A | G | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.242-934T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687396 | ||||||
| chr4:140687397
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0184 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.242-935T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687397 | ||||||
| chr4:140687403
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-941A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687403 | ||||||
| chr4:140687491
|
T | A | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-1029A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687491 | ||||||
| chr4:140687631
|
C | T | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-1169G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687631 | ||||||
| chr4:140688138
|
T | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0176others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.242-1676A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688138 | ||||||
| chr4:140688245
|
A | G | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-1783T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688245 | ||||||
| chr4:140688414
|
C | T | 28 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.242-1952G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688414 | ||||||
| chr4:140688496
|
A | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-2034T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688496 | ||||||
| chr4:140688497
|
T | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-2035A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688497 | ||||||
| chr4:140688608
|
G | A | 2 | a0001c0005t0001g0159a0001c0005t0009g0004 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.242-2146C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688608 | ||||||
| chr4:140688624
|
G | C | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-2162C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688624 | ||||||
| chr4:140688630
|
C | T | 2 | a0001c0004t0001g0228a0001c0004t0002g0260 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242-2168G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688630 | ||||||
| chr4:140688660
|
C | T | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.242-2198G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688660 | ||||||
| chr4:140688685
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.242-2223G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688685 | ||||||
| chr4:140689016
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.242-2554G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689016 | ||||||
| chr4:140689019
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.242-2557A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689019 | ||||||
| chr4:140689041
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-2579G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689041 | ||||||
| chr4:140689135
|
G | T | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.242-2673C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689135 | ||||||
| chr4:140689206
|
A | T | 1 | a0001c0007t0001g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.242-2744T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689206 | ||||||
| chr4:140689207
|
T | C | 36 | a0001c0004t0001g0045a0001c0004t0001g0103a0001c0004t0001g0107others(33): Show | 36 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.242-2745A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689207 | ||||||
| chr4:140689240
|
C | G | 1 | a0003c0019t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.242-2778G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689240 | ||||||
| chr4:140689315
|
T | C | 12 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(9): Show | 12 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-2853A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689315 | ||||||
| chr4:140689336
|
A | G | 5 | a0001c0004t0001g0224a0001c0007t0001g0218a0001c0007t0001g0219others(2): Show | 5 | HG02083.hp2 NA18963.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-2874T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689336 | ||||||
| chr4:140689376
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-2914C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689376 | ||||||
| chr4:140689393
|
C | T | 2 | a0001c0004t0001g0152a0001c0004t0001g0272 | 2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.242-2931G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689393 | ||||||
| chr4:140689401
|
CTTCCCTT others(12): Show |
C | 5 | a0001c0004t0001g0086a0001c0004t0001g0228a0001c0004t0002g0260others(2): Show | 5 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-2958_242-2940d others(21): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689401 | ||||||
| chr4:140689455
|
CCCCTT | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(217): Show | 220 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.242-2998_242-2994d others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689455 | ||||||
| chr4:140689460
|
T | TCCCTTCC others(137): Show |
2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.242-2999_242-2998i others(146): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689460 | ||||||
| chr4:140689515
|
CCT | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0160others(50): Show | 53 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.242-3055_242-3054d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689515 | ||||||
| chr4:140689603
|
C | T | 1 | a0001c0001t0004g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.242-3141G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689603 | ||||||
| chr4:140689649
|
CT | C | 33 | a0001c0002t0001g0137a0001c0004t0001g0045a0001c0004t0001g0103others(30): Show | 33 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.242-3188delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689649 | ||||||
| chr4:140689650
|
T | C | 3 | a0001c0004t0001g0119a0001c0004t0001g0272a0002c0009t0002g0047 | 3 | HG00408.hp2 HG02486.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.242-3188A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689650 | ||||||
| chr4:140689674
|
T | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(216): Show | 219 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.242-3212A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689674 | ||||||
| chr4:140689754
|
T | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(18): Show | 21 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.242-3292A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689754 | ||||||
| chr4:140689854
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-3392A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689854 | ||||||
| chr4:140690072
|
T | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.242-3610A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690072 | ||||||
| chr4:140690136
|
G | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0073 | 2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.242-3674C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690136 | ||||||
| chr4:140690171
|
G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.242-3709C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690171 | ||||||
| chr4:140690338
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.242-3876T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690338 | ||||||
| chr4:140690519
|
T | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(217): Show | 220 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.242-4057A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690519 | ||||||
| chr4:140690672
|
A | G | 1 | a0001c0003t0001g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.242-4210T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690672 | ||||||
| chr4:140690789
|
C | T | 3 | a0001c0001t0001g0002a0001c0002t0001g0244a0001c0005t0001g0114 | 3 | HG02145.hp1 HG03209.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.242-4327G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690789 | ||||||
| chr4:140690917
|
C | T | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.242-4455G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690917 | ||||||
| chr4:140691113
|
G | A | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.242-4651C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691113 | ||||||
| chr4:140691131
|
C | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.242-4669G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691131 | ||||||
| chr4:140691154
|
A | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.242-4692T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691154 | ||||||
| chr4:140691253
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.242-4791C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691253 | ||||||
| chr4:140691352
|
T | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0160a0001c0001t0001g0161others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-4890A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691352 | ||||||
| chr4:140691399
|
C | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0075 | 3 | HG00733.hp2 HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.242-4937G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691399 | ||||||
| chr4:140691566
|
C | T | 1 | a0001c0004t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.242-5104G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691566 | ||||||
| chr4:140691623
|
G | A | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.242-5161C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691623 | ||||||
| chr4:140692117
|
G | C | 1 | a0001c0001t0002g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.242-5655C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692117 | ||||||
| chr4:140692178
|
T | C | 3 | a0001c0004t0001g0228a0001c0004t0002g0260a0001c0005t0001g0114 | 3 | HG02145.hp1 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242-5716A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692178 | ||||||
| chr4:140692284
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.242-5822C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692284 | ||||||
| chr4:140692456
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.242-5994C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692456 | ||||||
| chr4:140692563
|
A | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0160a0001c0001t0001g0161others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-6101T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692563 | ||||||
| chr4:140692677
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.242-6215G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692677 | ||||||
| chr4:140692681
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-6219G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692681 | ||||||
| chr4:140692808
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.242-6346G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692808 | ||||||
| chr4:140692843
|
T | A | 136 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(133): Show | 137 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.242-6381A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692843 | ||||||
| chr4:140693030
|
A | T | 4 | a0001c0001t0001g0143a0001c0004t0001g0086a0001c0004t0005g0265others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-6568T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693030 | ||||||
| chr4:140693051
|
C | CA | 4 | a0001c0004t0001g0110a0001c0004t0001g0123a0001c0004t0001g0125others(1): Show | 4 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-6590dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693051 | ||||||
| chr4:140693130
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.242-6668G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693130 | ||||||
| chr4:140693142
|
T | C | 2 | a0001c0002t0001g0204a0001c0002t0001g0232 | 2 | HG02523.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.242-6680A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693142 | ||||||
| chr4:140693182
|
C | T | 18 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(15): Show | 18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-6720G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693182 | ||||||
| chr4:140693258
|
A | T | 1 | a0001c0004t0001g0136 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.242-6796T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693258 | ||||||
| chr4:140693290
|
T | A | 1 | a0001c0007t0001g0238 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.242-6828A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693290 | ||||||
| chr4:140693464
|
C | T | 2 | a0001c0002t0001g0244a0001c0021t0001g0264 | 2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.242-7002G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693464 | ||||||
| chr4:140693946
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.242-7484T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693946 | ||||||
| chr4:140694058
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.241+7446T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694058 | ||||||
| chr4:140694101
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(141): Show | 145 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.241+7403T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694101 | ||||||
| chr4:140694155
|
T | C | 1 | a0001c0002t0001g0232 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.241+7349A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694155 | ||||||
| chr4:140694212
|
C | T | 3 | a0001c0004t0001g0086a0001c0004t0005g0265a0001c0013t0011g0115 | 3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.241+7292G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694212 | ||||||
| chr4:140694463
|
C | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0153others(3): Show | 6 | HG02572.hp1 HG02922.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.241+7041G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694463 | ||||||
| chr4:140694570
|
CA | C | 90 | a0001c0001t0003g0288a0001c0002t0001g0050a0001c0002t0001g0064others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.241+6933delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694570 | ||||||
| chr4:140694717
|
G | A | 2 | a0001c0003t0001g0055a0001c0003t0001g0078 | 2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.241+6787C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694717 | ||||||
| chr4:140694734
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0160a0001c0001t0001g0161others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+6770T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694734 | ||||||
| chr4:140694796
|
T | TA | 144 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(141): Show | 145 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.241+6707_241+6708i others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694796 | ||||||
| chr4:140694848
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+6656A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694848 | ||||||
| chr4:140694879
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(4): Show | 7 | HG00544.hp1 HG01243.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.241+6625G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694879 | ||||||
| chr4:140694930
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(13): Show | 16 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.241+6574G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694930 | ||||||
| chr4:140694999
|
C | T | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.241+6505G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694999 | ||||||
| chr4:140695013
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0003g0278a0001c0001t0003g0279others(1): Show | 4 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+6491G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695013 | ||||||
| chr4:140695018
|
C | T | 3 | a0001c0004t0001g0086a0001c0004t0005g0265a0001c0013t0011g0115 | 3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.241+6486G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695018 | ||||||
| chr4:140695134
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(15): Show | 18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+6370T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695134 | ||||||
| chr4:140695340
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0160a0001c0001t0001g0161others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.241+6164T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695340 | ||||||
| chr4:140695664
|
A | C | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.241+5840T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695664 | ||||||
| chr4:140695664
|
A | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.241+5840T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695664 | ||||||
| chr4:140695782
|
T | G | 1 | a0001c0001t0003g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.241+5722A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695782 | ||||||
| chr4:140695803
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(137): Show | 141 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.241+5701T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695803 | ||||||
| chr4:140695825
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0160a0001c0001t0001g0161others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.241+5679G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695825 | ||||||
| chr4:140695840
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+5664G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695840 | ||||||
| chr4:140695902
|
A | G | 4 | a0001c0001t0001g0143a0001c0004t0001g0086a0001c0004t0005g0265others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+5602T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695902 | ||||||
| chr4:140695996
|
T | A | 13 | a0001c0004t0001g0045a0001c0004t0001g0119a0001c0004t0001g0121others(10): Show | 13 | HG00408.hp2 NA18964.hp1 NA18966.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+5508A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695996 | ||||||
| chr4:140696025
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.241+5479T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696025 | ||||||
| chr4:140696175
|
GGGCCAGG others(6): Show |
G | 86 | a0001c0002t0001g0050a0001c0002t0001g0064a0001c0002t0001g0094others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.241+5316_241+5328d others(15): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696175 | ||||||
| chr4:140696176
|
G | A | 34 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(31): Show | 34 | HG00639.hp1 HG01192.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.241+5328C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696176 | ||||||
| chr4:140696193
|
CACGCCT | C | 86 | a0001c0002t0001g0050a0001c0002t0001g0064a0001c0002t0001g0094others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.241+5305_241+5310d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696193 | ||||||
| chr4:140696286
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.241+5218C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696286 | ||||||
| chr4:140696437
|
C | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.241+5067G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696437 | ||||||
| chr4:140696454
|
T | G | 1 | a0001c0017t0001g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.241+5050A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696454 | ||||||
| chr4:140696455
|
C | CA | 91 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.241+5048dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | ||||||
| chr4:140696455
|
C | CAA | 31 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0019others(28): Show | 31 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.241+5047_241+5048d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | ||||||
| chr4:140696455
|
CA | C | 17 | a0001c0001t0001g0161a0001c0001t0001g0270a0001c0001t0017g0297others(14): Show | 17 | HG00609.hp2 HG00673.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.241+5048delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | ||||||
| chr4:140696455
|
CAA | C | 92 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.241+5047_241+5048d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | ||||||
| chr4:140696498
|
T | C | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.241+5006A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696498 | ||||||
| chr4:140696596
|
G | C | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.241+4908C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696596 | ||||||
| chr4:140696616
|
C | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.241+4888G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696616 | ||||||
| chr4:140696854
|
G | A | 1 | a0001c0003t0001g0068 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.241+4650C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696854 | ||||||
| chr4:140696925
|
A | T | 24 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(21): Show | 24 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.241+4579T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696925 | ||||||
| chr4:140696944
|
T | C | 1 | a0001c0008t0005g0241 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.241+4560A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696944 | ||||||
| chr4:140696985
|
T | C | 1 | a0001c0004t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.241+4519A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696985 | ||||||
| chr4:140697084
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(15): Show | 18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+4420T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697084 | ||||||
| chr4:140697279
|
G | A | 2 | a0001c0001t0001g0002a0001c0005t0001g0114 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.241+4225C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697279 | ||||||
| chr4:140697440
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241+4064G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697440 | ||||||
| chr4:140697676
|
A | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.241+3828T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697676 | ||||||
| chr4:140697807
|
A | G | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.241+3697T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697807 | ||||||
| chr4:140698166
|
C | CT | 16 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(13): Show | 16 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.241+3337dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698166 | ||||||
| chr4:140698278
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.241+3226G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698278 | ||||||
| chr4:140698379
|
C | T | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.241+3125G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698379 | ||||||
| chr4:140698380
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241+3124C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698380 | ||||||
| chr4:140698489
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.241+3015C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698489 | ||||||
| chr4:140698546
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+2958C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698546 | ||||||
| chr4:140698653
|
G | A | 32 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(29): Show | 32 | HG00639.hp1 HG01192.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.241+2851C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698653 | ||||||
| chr4:140698714
|
G | A | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(49): Show | 52 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.241+2790C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698714 | ||||||
| chr4:140698722
|
AGTGAGAC others(14): Show |
A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.241+2761_241+2781d others(23): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698722 | ||||||
| chr4:140698746
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.241+2758C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698746 | ||||||
| chr4:140698746
|
G | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.241+2758C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698746 | ||||||
| chr4:140698748
|
G | A | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.241+2756C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698748 | ||||||
| chr4:140698992
|
G | A | 17 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.241+2512C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698992 | ||||||
| chr4:140699034
|
T | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0181 | 3 | HG03704.hp1 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+2470A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699034 | ||||||
| chr4:140699349
|
A | G | 1 | a0001c0005t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.241+2155T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699349 | ||||||
| chr4:140699435
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0162 | 3 | HG00741.hp2 HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.241+2069C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699435 | ||||||
| chr4:140699533
|
C | T | 14 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(11): Show | 14 | HG01106.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+1971G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699533 | ||||||
| chr4:140699622
|
G | T | 2 | a0001c0020t0001g0187a0001c0021t0001g0264 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.241+1882C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699622 | ||||||
| chr4:140699687
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+1817G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699687 | ||||||
| chr4:140699762
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.241+1742C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699762 | ||||||
| chr4:140699777
|
T | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.241+1727A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699777 | ||||||
| chr4:140699849
|
G | T | 10 | a0001c0001t0001g0003a0001c0004t0001g0086a0001c0004t0001g0228others(7): Show | 10 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.241+1655C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699849 | ||||||
| chr4:140699933
|
T | TA | 11 | a0001c0001t0001g0143a0001c0005t0001g0128a0001c0005t0001g0129others(8): Show | 11 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+1570dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699933 | ||||||
| chr4:140699971
|
G | C | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.241+1533C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699971 | ||||||
| chr4:140700008
|
C | T | 1 | a0001c0007t0001g0118 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.241+1496G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700008 | ||||||
| chr4:140700021
|
T | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.241+1483A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700021 | ||||||
| chr4:140700085
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241+1419G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700085 | ||||||
| chr4:140700110
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0049others(16): Show | 19 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.241+1394T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700110 | ||||||
| chr4:140700151
|
T | TA | 6 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+1352dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700151 | ||||||
| chr4:140700163
|
T | A | 2 | a0001c0001t0001g0217a0001c0003t0001g0216 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.241+1341A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700163 | ||||||
| chr4:140700214
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1290A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700214 | ||||||
| chr4:140700215
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1289A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700215 | ||||||
| chr4:140700216
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1288C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700216 | ||||||
| chr4:140700220
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1284C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700220 | ||||||
| chr4:140700225
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(145): Show | 149 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.241+1279C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700225 | ||||||
| chr4:140700310
|
C | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0222 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.241+1194G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700310 | ||||||
| chr4:140700404
|
C | T | 1 | a0001c0010t0001g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.241+1100G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700404 | ||||||
| chr4:140700449
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0165others(12): Show | 15 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.241+1054dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700449 | ||||||
| chr4:140700450
|
A | C | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+1054T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700450 | ||||||
| chr4:140700460
|
C | A | 1 | a0001c0003t0001g0055 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.241+1044G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700460 | ||||||
| chr4:140700474
|
C | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(176): Show | 180 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(177): Show |
intron_variant | MODIFIER | c.241+1030G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700474 | ||||||
| chr4:140700531
|
T | A | 3 | a0001c0001t0001g0143a0001c0005t0001g0114a0001c0008t0003g0276 | 3 | HG02145.hp1 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.241+973A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700531 | ||||||
| chr4:140700533
|
T | C | 1 | a0001c0015t0002g0084 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.241+971A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700533 | ||||||
| chr4:140700553
|
C | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.241+951G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700553 | ||||||
| chr4:140700608
|
G | A | 2 | a0001c0005t0001g0114a0001c0008t0003g0276 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.241+896C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700608 | ||||||
| chr4:140700637
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.241+867T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700637 | ||||||
| chr4:140700815
|
G | A | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+689C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700815 | ||||||
| chr4:140700821
|
G | GA | 12 | a0001c0001t0001g0248a0001c0003t0001g0055a0001c0005t0001g0128others(9): Show | 12 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.241+682dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700821 | ||||||
| chr4:140700821
|
GA | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(15): Show | 18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+682delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700821 | ||||||
| chr4:140700934
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0049others(16): Show | 19 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.241+570C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700934 | ||||||
| chr4:140700974
|
C | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(146): Show | 150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.241+530G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700974 | ||||||
| chr4:140701095
|
C | T | 1 | a0001c0001t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241+409G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701095 | ||||||
| chr4:140701217
|
A | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(157): Show | 161 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(158): Show |
intron_variant | MODIFIER | c.241+287T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701217 | ||||||
| chr4:140701239
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.241+265G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701239 | ||||||
| chr4:140701281
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0082 | 2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.241+223C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701281 | ||||||
| chr4:140701282
|
G | A | 5 | a0001c0004t0001g0086a0001c0004t0005g0265a0001c0008t0001g0240others(2): Show | 5 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+222C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701282 | ||||||
| chr4:140701317
|
G | C | 1 | a0001c0005t0001g0128 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241+187C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701317 | ||||||
| chr4:140701665
|
C | T | 14 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(11): Show | 14 | HG01106.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-51G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701665 | ||||||
| chr4:140701849
|
CA | C | 102 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0161others(99): Show | 103 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.131-236delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701849 | ||||||
| chr4:140701906
|
G | C | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-292C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701906 | ||||||
| chr4:140701909
|
C | A | 8 | a0001c0001t0001g0161a0001c0001t0001g0266a0001c0001t0001g0270others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-295G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701909 | ||||||
| chr4:140702120
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-506G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702120 | ||||||
| chr4:140702187
|
G | C | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-573C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702187 | ||||||
| chr4:140702439
|
G | C | 1 | a0001c0003t0001g0096 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.131-825C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702439 | ||||||
| chr4:140702504
|
G | A | 10 | a0001c0001t0001g0003a0001c0004t0001g0086a0001c0004t0001g0228others(7): Show | 10 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-890C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702504 | ||||||
| chr4:140702631
|
T | C | 11 | a0001c0001t0001g0143a0001c0005t0001g0128a0001c0005t0001g0129others(8): Show | 11 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-1017A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702631 | ||||||
| chr4:140702636
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.131-1022T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702636 | ||||||
| chr4:140702773
|
C | T | 93 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0184others(90): Show | 94 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.131-1159G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702773 | ||||||
| chr4:140702954
|
T | G | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-1340A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702954 | ||||||
| chr4:140703025
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-1411A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703025 | ||||||
| chr4:140703111
|
G | A | 2 | a0001c0005t0001g0114a0001c0008t0003g0276 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-1497C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703111 | ||||||
| chr4:140703278
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.131-1664G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703278 | ||||||
| chr4:140703304
|
T | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(146): Show | 150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.131-1690A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703304 | ||||||
| chr4:140703328
|
G | A | 1 | a0001c0001t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.131-1714C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703328 | ||||||
| chr4:140703378
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0003g0278a0001c0001t0003g0282 | 3 | HG01257.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.131-1764C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703378 | ||||||
| chr4:140703399
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-1785A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703399 | ||||||
| chr4:140703433
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131-1819T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703433 | ||||||
| chr4:140703447
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0049others(15): Show | 18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.131-1833G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703447 | ||||||
| chr4:140703458
|
A | C | 1 | a0001c0002t0001g0232 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.131-1844T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703458 | ||||||
| chr4:140703490
|
TGTGGA | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-1881_131-1877d others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703490 | ||||||
| chr4:140703519
|
C | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(146): Show | 150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.131-1905G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703519 | ||||||
| chr4:140703577
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.131-1963T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703577 | ||||||
| chr4:140703581
|
T | C | 17 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-1967A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703581 | ||||||
| chr4:140703607
|
T | G | 2 | a0001c0002t0001g0180a0001c0002t0001g0242 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.131-1993A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703607 | ||||||
| chr4:140703824
|
G | A | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-2210C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703824 | ||||||
| chr4:140704063
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(146): Show | 150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.131-2449C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704063 | ||||||
| chr4:140704126
|
G | A | 2 | a0001c0002t0001g0180a0001c0002t0001g0242 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.131-2512C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704126 | ||||||
| chr4:140704136
|
A | C | 1 | a0001c0006t0001g0261 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.131-2522T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704136 | ||||||
| chr4:140704142
|
A | T | 1 | a0001c0006t0001g0261 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.131-2528T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704142 | ||||||
| chr4:140704144
|
T | A | 1 | a0001c0006t0001g0261 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.131-2530A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704144 | ||||||
| chr4:140704207
|
G | A | 2 | a0001c0002t0002g0231a0001c0002t0003g0275 | 2 | HG01081.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.131-2593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704207 | ||||||
| chr4:140704332
|
C | T | 2 | a0001c0020t0001g0187a0001c0021t0001g0264 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-2718G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704332 | ||||||
| chr4:140704333
|
G | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01517.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-2719C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704333 | ||||||
| chr4:140704356
|
A | G | 2 | a0001c0020t0001g0187a0001c0021t0001g0264 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-2742T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704356 | ||||||
| chr4:140704392
|
C | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(38): Show | 41 | HG01106.hp2 HG01192.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.131-2778G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704392 | ||||||
| chr4:140704399
|
T | TCAAA | 145 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(142): Show | 146 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.131-2789_131-2786d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704399 | ||||||
| chr4:140704435
|
G | GA | 46 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0019others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.131-2822dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704435 | ||||||
| chr4:140704435
|
GA | G | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0090others(106): Show | 110 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.131-2822delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704435 | ||||||
| chr4:140704513
|
C | G | 1 | a0001c0004t0001g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.131-2899G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704513 | ||||||
| chr4:140704568
|
G | C | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-2954C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704568 | ||||||
| chr4:140704741
|
A | G | 22 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(19): Show | 22 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-3127T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704741 | ||||||
| chr4:140704743
|
T | C | 11 | a0001c0001t0001g0143a0001c0005t0001g0128a0001c0005t0001g0129others(8): Show | 11 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-3129A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704743 | ||||||
| chr4:140704830
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.131-3216T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704830 | ||||||
| chr4:140704846
|
G | A | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-3232C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704846 | ||||||
| chr4:140704941
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.131-3327A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704941 | ||||||
| chr4:140704950
|
G | A | 6 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-3336C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704950 | ||||||
| chr4:140705008
|
A | G | 1 | a0001c0003t0001g0083 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.131-3394T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705008 | ||||||
| chr4:140705343
|
A | T | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-3729T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705343 | ||||||
| chr4:140705503
|
GGTGTGTG others(7): Show |
G | 1 | a0001c0002t0001g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-3903_131-3890d others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705503 | ||||||
| chr4:140705511
|
CATGT | C | 3 | a0001c0005t0001g0131a0001c0005t0001g0132a0001c0005t0001g0133 | 3 | HG02630.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.131-3901_131-3898d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705511 | ||||||
| chr4:140705512
|
ATG | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.131-3900_131-3899d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705512 | ||||||
| chr4:140705512
|
ATGTG | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0176others(19): Show | 22 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-3902_131-3899d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705512 | ||||||
| chr4:140705512
|
ATGTGTGT others(3): Show |
A | 22 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(19): Show | 22 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-3908_131-3899d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705512 | ||||||
| chr4:140705522
|
G | GTGTA | 17 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(14): Show | 17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-3909_131-3908i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705522 | ||||||
| chr4:140705541
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.131-3927A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705541 | ||||||
| chr4:140705953
|
T | C | 3 | a0001c0004t0001g0086a0001c0004t0005g0265a0001c0013t0011g0115 | 3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.131-4339A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705953 | ||||||
| chr4:140706025
|
A | C | 2 | a0001c0004t0001g0228a0001c0004t0002g0260 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.131-4411T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706025 | ||||||
| chr4:140706070
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.131-4456A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706070 | ||||||
| chr4:140706179
|
C | T | 2 | a0001c0008t0001g0240a0001c0008t0005g0241 | 2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.131-4565G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706179 | ||||||
| chr4:140706445
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-4831G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706445 | ||||||
| chr4:140706709
|
T | A | 1 | a0001c0001t0003g0282 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.131-5095A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706709 | ||||||
| chr4:140706903
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.131-5289T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706903 | ||||||
| chr4:140706946
|
C | T | 22 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(19): Show | 22 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-5332G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706946 | ||||||
| chr4:140706947
|
G | A | 10 | a0001c0001t0001g0003a0001c0004t0001g0086a0001c0004t0001g0228others(7): Show | 10 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-5333C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706947 | ||||||
| chr4:140707018
|
A | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.131-5404T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707018 | ||||||
| chr4:140707050
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-5436T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707050 | ||||||
| chr4:140707088
|
C | G | 1 | a0001c0005t0001g0128 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.131-5474G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707088 | ||||||
| chr4:140707128
|
GT | G | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.131-5515delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707128 | ||||||
| chr4:140707568
|
T | C | 28 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(25): Show | 28 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-5954A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707568 | ||||||
| chr4:140707617
|
G | A | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-6003C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707617 | ||||||
| chr4:140707680
|
G | C | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-6066C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707680 | ||||||
| chr4:140707751
|
G | T | 42 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0090others(39): Show | 42 | HG01192.hp1 HG01257.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.131-6137C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707751 | ||||||
| chr4:140707761
|
A | G | 103 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0161others(100): Show | 104 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.131-6147T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707761 | ||||||
| chr4:140708022
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.131-6408T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708022 | ||||||
| chr4:140708475
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.131-6861G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708475 | ||||||
| chr4:140708485
|
T | C | 2 | a0001c0005t0001g0114a0001c0008t0003g0276 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-6871A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708485 | ||||||
| chr4:140708599
|
G | A | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-6985C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708599 | ||||||
| chr4:140708616
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-7002G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708616 | ||||||
| chr4:140708631
|
C | T | 6 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-7017G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708631 | ||||||
| chr4:140708672
|
C | T | 7 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0002g0101others(4): Show | 7 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-7058G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708672 | ||||||
| chr4:140708739
|
T | C | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-7125A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708739 | ||||||
| chr4:140708772
|
T | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.131-7158A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708772 | ||||||
| chr4:140708983
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-7369C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708983 | ||||||
| chr4:140709012
|
G | A | 3 | a0001c0004t0001g0142a0001c0020t0001g0187a0001c0021t0001g0264 | 3 | HG03139.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-7398C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709012 | ||||||
| chr4:140709219
|
A | ATC | 66 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-7607_131-7606d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709219
|
A | ATCTC | 19 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0052others(16): Show | 19 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.131-7609_131-7606d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709219
|
A | ATCTCTC | 8 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0057others(5): Show | 8 | HG02004.hp2 HG02155.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-7611_131-7606d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709219
|
A | ATCTCTCT others(1): Show |
5 | a0001c0001t0001g0061a0001c0003t0001g0008a0001c0003t0001g0022others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-7613_131-7606d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709219
|
A | ATCTCTCT others(3): Show |
3 | a0001c0001t0001g0033a0001c0001t0002g0243a0001c0003t0001g0021 | 3 | HG01175.hp2 HG01943.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.131-7615_131-7606d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709219
|
A | ATCTCTCT others(5): Show |
1 | a0001c0001t0001g0034 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.131-7617_131-7606d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709219
|
ATC | A | 4 | a0001c0001t0001g0003a0001c0001t0004g0294a0001c0004t0001g0135others(1): Show | 4 | HG00741.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-7607_131-7606d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | ||||||
| chr4:140709238
|
TCTCTCTC others(5): Show |
T | 4 | a0001c0004t0001g0086a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-7636_131-7625d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709238 | ||||||
| chr4:140709240
|
TCTCTCTC others(3): Show |
T | 2 | a0001c0004t0001g0228a0001c0004t0002g0260 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.131-7636_131-7627d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709240 | ||||||
| chr4:140709242
|
TCTCTCTC others(3): Show |
T | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-7638_131-7629d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709242 | ||||||
| chr4:140709244
|
T | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0151others(5): Show | 8 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-7630A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | ||||||
| chr4:140709244
|
T | TCACA | 7 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0153others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-7631_131-7630i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | ||||||
| chr4:140709244
|
T | TCACACA | 3 | a0001c0001t0001g0090a0001c0001t0001g0138a0001c0001t0001g0161 | 3 | HG01891.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.131-7631_131-7630i others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | ||||||
| chr4:140709244
|
TCTCTCA | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0049others(11): Show | 14 | HG01975.hp1 HG01978.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.131-7636_131-7631d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | ||||||
| chr4:140709244
|
TCTCTCAC others(5): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.131-7642_131-7631d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | ||||||
| chr4:140709246
|
T | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0138others(20): Show | 23 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-7632A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709246 | ||||||
| chr4:140709246
|
T | TCACA | 7 | a0001c0001t0001g0092a0001c0004t0001g0119a0001c0004t0001g0121others(4): Show | 7 | HG00408.hp2 HG02809.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-7633_131-7632i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709246 | ||||||
| chr4:140709248
|
T | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(46): Show | 49 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-7634A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCA | 3 | a0001c0001t0001g0270a0001c0002t0015g0280a0001c0004t0001g0142 | 3 | HG03139.hp2 HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.131-7636_131-7635d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCACACA | 3 | a0001c0001t0002g0269a0001c0004t0001g0272a0001c0006t0001g0257 | 3 | HG02486.hp1 HG02647.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.131-7640_131-7635d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0020t0001g0187 | 3 | HG01070.hp2 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.131-7644_131-7635d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCACA | 5 | a0001c0001t0005g0095a0001c0002t0001g0173a0001c0002t0001g0215others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-7635_131-7634i others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCACAC others(3): Show |
1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-7635_131-7634i others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCAC others(3): Show |
2 | a0001c0002t0001g0195a0001c0012t0008g0146 | 2 | HG01496.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.131-7635_131-7634i others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCAC others(5): Show |
2 | a0001c0001t0001g0266a0001c0008t0001g0183 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.131-7635_131-7634i others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCAC others(9): Show |
1 | a0001c0002t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.131-7635_131-7634i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCTC others(5): Show |
1 | a0001c0001t0001g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.131-7635_131-7634i others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCTC others(9): Show |
1 | a0001c0002t0006g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.131-7635_131-7634i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCTC others(11): Show |
2 | a0001c0002t0001g0097a0001c0002t0001g0098 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.131-7635_131-7634i others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCTC others(13): Show |
1 | a0001c0002t0001g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.131-7635_131-7634i others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
T | TCTCTCTC others(9): Show |
1 | a0001c0002t0006g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-7635_131-7634i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
TCA | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.131-7636_131-7635d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
TCACA | T | 3 | a0001c0001t0001g0044a0001c0008t0003g0276a0001c0016t0012g0271 | 3 | HG00609.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-7638_131-7635d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
TCACACAC others(1): Show |
T | 8 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-7642_131-7635d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709248
|
TCACACAC others(7): Show |
T | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-7648_131-7635d others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | ||||||
| chr4:140709250
|
A | T | 83 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.131-7636T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709250 | ||||||
| chr4:140709252
|
A | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.131-7638T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709252 | ||||||
| chr4:140709254
|
A | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(60): Show | 63 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.131-7640T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709254 | ||||||
| chr4:140709256
|
A | T | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(50): Show | 53 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.131-7642T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709256 | ||||||
| chr4:140709258
|
A | T | 2 | a0001c0001t0001g0063a0001c0003t0001g0085 | 2 | HG03491.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.131-7644T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709258 | ||||||
| chr4:140709260
|
A | T | 1 | a0001c0003t0001g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.131-7646T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709260 | ||||||
| chr4:140709283
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-7669G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709283 | ||||||
| chr4:140709288
|
A | C | 2 | a0001c0001t0003g0286a0001c0002t0002g0231 | 2 | HG01975.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.131-7674T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709288 | ||||||
| chr4:140709308
|
G | A | 1 | a0001c0006t0001g0263 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.131-7694C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709308 | ||||||
| chr4:140709414
|
G | A | 1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-7800C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709414 | ||||||
| chr4:140709454
|
T | C | 24 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(21): Show | 24 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.131-7840A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709454 | ||||||
| chr4:140709502
|
T | TA | 78 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(75): Show | 78 | HG00639.hp1 HG01106.hp2 HG01192.hp1 others(75): Show |
intron_variant | MODIFIER | c.131-7889dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709502 | ||||||
| chr4:140709502
|
TA | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.131-7889delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709502 | ||||||
| chr4:140709664
|
A | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(74): Show | 77 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.131-8050T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709664 | ||||||
| chr4:140709706
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.131-8092G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709706 | ||||||
| chr4:140709807
|
A | G | 1 | a0001c0001t0004g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.131-8193T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709807 | ||||||
| chr4:140709874
|
T | A | 1 | a0001c0010t0001g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.131-8260A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709874 | ||||||
| chr4:140709901
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-8287C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709901 | ||||||
| chr4:140710104
|
T | G | 2 | a0001c0001t0014g0284a0001c0003t0003g0285 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.131-8490A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710104 | ||||||
| chr4:140710202
|
G | A | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-8588C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710202 | ||||||
| chr4:140710474
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.131-8860G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710474 | ||||||
| chr4:140710563
|
A | G | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-8949T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710563 | ||||||
| chr4:140710576
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-8962G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710576 | ||||||
| chr4:140710619
|
G | A | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131-9005C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710619 | ||||||
| chr4:140710651
|
C | G | 10 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0001g0131others(7): Show | 10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-9037G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710651 | ||||||
| chr4:140711009
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.131-9395C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711009 | ||||||
| chr4:140711150
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.131-9536G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711150 | ||||||
| chr4:140711157
|
T | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(24): Show | 27 | HG01257.hp1 HG01261.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-9543A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711157 | ||||||
| chr4:140711349
|
T | C | 1 | a0001c0008t0003g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.131-9735A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711349 | ||||||
| chr4:140711385
|
C | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0002t0002g0091 | 3 | HG02615.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.131-9771G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711385 | ||||||
| chr4:140711434
|
G | C | 12 | a0001c0001t0001g0003a0001c0001t0002g0274a0001c0004t0001g0086others(9): Show | 12 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-9820C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711434 | ||||||
| chr4:140711470
|
C | G | 24 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(21): Show | 24 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.131-9856G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711470 | ||||||
| chr4:140711536
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(25): Show | 28 | HG01257.hp1 HG01261.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-9922G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711536 | ||||||
| chr4:140711550
|
C | A | 28 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0049others(25): Show | 28 | HG01257.hp1 HG01261.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-9936G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711550 | ||||||
| chr4:140711791
|
C | T | 1 | a0001c0002t0001g0189 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.131-10177G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711791 | ||||||
| chr4:140711819
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(12): Show | 15 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.131-10205G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711819 | ||||||
| chr4:140711857
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.131-10243C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711857 | ||||||
| chr4:140711939
|
A | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.131-10325T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711939 | ||||||
| chr4:140711947
|
A | G | 3 | a0001c0002t0001g0173a0001c0002t0003g0281a0001c0002t0003g0290 | 3 | HG01074.hp2 HG02559.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.131-10333T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711947 | ||||||
| chr4:140712080
|
C | T | 22 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(19): Show | 22 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-10466G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712080 | ||||||
| chr4:140712150
|
G | A | 1 | a0001c0005t0002g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.131-10536C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712150 | ||||||
| chr4:140712153
|
CATATCTA others(289): Show |
C | 15 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0139others(12): Show | 15 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.131-10835_131-1054 others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712153 | ||||||
| chr4:140712291
|
T | C | 23 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-10677A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712291 | ||||||
| chr4:140712298
|
A | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.131-10684T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712298 | ||||||
| chr4:140712381
|
C | A | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-10767G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712381 | ||||||
| chr4:140712438
|
T | A | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-10824A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712438 | ||||||
| chr4:140712449
|
A | AAATATAT others(40): Show |
1 | a0001c0007t0001g0218 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.131-10836_131-1083 others(51): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0266 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.131-10845_131-1083 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(5): Show |
30 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0033others(27): Show | 30 | HG00140.hp1 HG00621.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-10847_131-1083 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(7): Show |
48 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 48 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(9): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0143a0001c0001t0002g0013others(2): Show | 5 | NA18953.hp2 NA18981.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(11): Show |
18 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(13): Show |
6 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0002g0089others(3): Show | 6 | HG01192.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(15): Show |
7 | a0001c0001t0001g0155a0001c0001t0002g0274a0001c0002t0001g0189others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(26): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(41): Show |
1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-10836_131-1083 others(52): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(17): Show |
1 | a0001c0002t0006g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.131-10836_131-1083 others(28): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(19): Show |
4 | a0001c0001t0001g0212a0001c0001t0003g0287a0001c0001t0003g0288others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(30): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(21): Show |
12 | a0001c0001t0001g0160a0001c0002t0001g0173a0001c0002t0001g0188others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(23): Show |
19 | a0001c0001t0001g0201a0001c0001t0006g0141a0001c0001t0014g0284others(16): Show | 19 | HG01169.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(34): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(25): Show |
35 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0169others(32): Show | 36 | HG00609.hp2 HG00639.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(36): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(27): Show |
27 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0217others(24): Show | 27 | HG00639.hp2 HG00673.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(38): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(29): Show |
18 | a0001c0001t0001g0161a0001c0001t0001g0184a0001c0001t0001g0198others(15): Show | 18 | HG01069.hp2 HG01346.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(40): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(31): Show |
3 | a0001c0001t0001g0028a0001c0003t0001g0216a0001c0008t0005g0241 | 3 | HG01261.hp2 HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.131-10836_131-1083 others(42): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(33): Show |
10 | a0001c0001t0001g0208a0001c0002t0001g0111a0001c0002t0001g0207others(7): Show | 10 | HG01891.hp2 HG02300.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(44): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(35): Show |
2 | a0001c0007t0001g0219a0001c0007t0001g0229 | 2 | NA18963.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.131-10836_131-1083 others(46): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | AATATATA others(39): Show |
1 | a0001c0002t0001g0221 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.131-10836_131-1083 others(50): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712449
|
A | ATTATATA others(25): Show |
2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-10836_131-1083 others(36): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | ||||||
| chr4:140712470
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.131-10856G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712470 | ||||||
| chr4:140712513
|
C | T | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-10899G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712513 | ||||||
| chr4:140712674
|
G | A | 1 | a0001c0001t0003g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.131-11060C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712674 | ||||||
| chr4:140712748
|
A | AATAG | 19 | a0001c0001t0001g0093a0001c0001t0001g0194a0001c0001t0001g0270others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.131-11138_131-1113 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | ||||||
| chr4:140712748
|
A | AATAGATA others(1): Show |
86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(83): Show | 86 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.131-11142_131-1113 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | ||||||
| chr4:140712748
|
A | AATAGATA others(5): Show |
55 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 55 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.131-11146_131-1113 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | ||||||
| chr4:140712748
|
A | AATAGATA others(9): Show |
1 | a0001c0001t0001g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.131-11150_131-1113 others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | ||||||
| chr4:140712748
|
AATAG | A | 12 | a0001c0001t0005g0095a0001c0002t0001g0097a0001c0002t0001g0098others(9): Show | 12 | HG00735.hp1 HG01884.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-11138_131-1113 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | ||||||
| chr4:140712748
|
AATAGATA others(1): Show |
A | 94 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0116others(91): Show | 95 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.131-11142_131-1113 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | ||||||
| chr4:140712932
|
C | G | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-11318G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712932 | ||||||
| chr4:140713150
|
C | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.131-11536G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713150 | ||||||
| chr4:140713294
|
T | C | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-11680A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713294 | ||||||
| chr4:140713303
|
C | T | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-11689G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713303 | ||||||
| chr4:140713390
|
G | A | 1 | a0001c0001t0004g0294 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-11776C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713390 | ||||||
| chr4:140713749
|
T | TA | 133 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.131-12136dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | ||||||
| chr4:140713749
|
T | TAA | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.131-12137_131-1213 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | ||||||
| chr4:140713749
|
T | TAAA | 26 | a0001c0001t0001g0049a0001c0001t0001g0139a0001c0001t0001g0140others(23): Show | 26 | HG01106.hp2 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.131-12138_131-1213 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | ||||||
| chr4:140713749
|
T | TAAAA | 8 | a0001c0001t0001g0003a0001c0001t0002g0274a0001c0004t0001g0086others(5): Show | 8 | HG01261.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-12139_131-1213 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | ||||||
| chr4:140713759
|
A | AAAC | 7 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0002g0101others(4): Show | 7 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-12148_131-1214 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713759 | ||||||
| chr4:140713843
|
T | C | 2 | a0001c0005t0001g0114a0001c0008t0003g0276 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-12229A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713843 | ||||||
| chr4:140713846
|
A | G | 3 | a0001c0004t0001g0103a0001c0004t0001g0107a0001c0007t0007g0106 | 3 | HG00558.hp2 NA18981.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.131-12232T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713846 | ||||||
| chr4:140713939
|
A | T | 1 | a0001c0003t0003g0285 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.131-12325T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713939 | ||||||
| chr4:140714167
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.131-12553G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714167 | ||||||
| chr4:140714179
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.131-12565A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714179 | ||||||
| chr4:140714224
|
T | C | 1 | a0001c0002t0001g0230 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.131-12610A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714224 | ||||||
| chr4:140714251
|
C | T | 7 | a0001c0001t0002g0182a0001c0002t0001g0195a0001c0002t0001g0245others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-12637G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714251 | ||||||
| chr4:140714311
|
G | T | 8 | a0001c0001t0001g0003a0001c0001t0002g0274a0001c0004t0001g0086others(5): Show | 8 | HG01261.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-12697C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714311 | ||||||
| chr4:140714406
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.131-12792G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714406 | ||||||
| chr4:140714445
|
C | T | 1 | a0001c0002t0001g0202 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.131-12831G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714445 | ||||||
| chr4:140714450
|
G | T | 104 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0116others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.131-12836C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714450 | ||||||
| chr4:140714493
|
T | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.131-12879A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714493 | ||||||
| chr4:140714700
|
T | C | 7 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0002g0101others(4): Show | 7 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-13086A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714700 | ||||||
| chr4:140714778
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131-13164C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714778 | ||||||
| chr4:140714833
|
G | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-13219C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714833 | ||||||
| chr4:140715103
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.131-13489C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715103 | ||||||
| chr4:140715167
|
C | T | 1 | a0001c0017t0001g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.131-13553G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715167 | ||||||
| chr4:140715257
|
C | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.131-13643G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715257 | ||||||
| chr4:140715269
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-13655G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715269 | ||||||
| chr4:140715496
|
C | T | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-13882G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715496 | ||||||
| chr4:140715607
|
A | G | 6 | a0001c0004t0001g0224a0001c0007t0001g0218a0001c0007t0001g0219others(3): Show | 6 | HG02083.hp2 NA18963.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-13993T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715607 | ||||||
| chr4:140715609
|
T | G | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131-13995A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715609 | ||||||
| chr4:140715611
|
T | C | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-13997A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715611 | ||||||
| chr4:140715778
|
A | C | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.131-14164T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715778 | ||||||
| chr4:140716016
|
C | T | 1 | a0001c0004t0001g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.131-14402G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716016 | ||||||
| chr4:140716121
|
T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-14507A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716121 | ||||||
| chr4:140716130
|
C | A | 6 | a0001c0004t0001g0224a0001c0007t0001g0218a0001c0007t0001g0219others(3): Show | 6 | HG02083.hp2 NA18963.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-14516G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716130 | ||||||
| chr4:140716324
|
C | CAAAAAGT others(312): Show |
1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-14711_131-1471 others(323): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716324 | ||||||
| chr4:140716507
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.131-14893T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716507 | ||||||
| chr4:140716574
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.131-14960A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716574 | ||||||
| chr4:140716600
|
T | C | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-14986A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716600 | ||||||
| chr4:140716623
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.131-15009G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716623 | ||||||
| chr4:140716921
|
T | TA | 102 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.131-15308dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716921 | ||||||
| chr4:140717014
|
C | T | 12 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(9): Show | 12 | HG01257.hp1 HG01975.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-15400G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717014 | ||||||
| chr4:140717082
|
A | G | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-15468T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717082 | ||||||
| chr4:140717271
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.131-15657C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717271 | ||||||
| chr4:140717429
|
T | C | 1 | a0001c0002t0001g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.131-15815A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717429 | ||||||
| chr4:140717586
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-15972C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717586 | ||||||
| chr4:140717608
|
T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-15994A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717608 | ||||||
| chr4:140717636
|
T | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0002g0274others(5): Show | 8 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-16022A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717636 | ||||||
| chr4:140717839
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.131-16225G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717839 | ||||||
| chr4:140717918
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-16304A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717918 | ||||||
| chr4:140718247
|
G | GA | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.131-16634dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718247 | ||||||
| chr4:140718304
|
C | T | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-16690G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718304 | ||||||
| chr4:140718345
|
T | G | 2 | a0001c0005t0001g0145a0001c0005t0001g0157 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.131-16731A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718345 | ||||||
| chr4:140718449
|
A | G | 1 | a0001c0002t0002g0220 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.131-16835T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718449 | ||||||
| chr4:140718489
|
C | A | 1 | a0001c0002t0015g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-16875G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718489 | ||||||
| chr4:140718560
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-16946G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718560 | ||||||
| chr4:140718633
|
C | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0270a0001c0001t0002g0269others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-17019G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718633 | ||||||
| chr4:140718637
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-17023A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718637 | ||||||
| chr4:140718936
|
T | A | 4 | a0001c0001t0014g0284a0001c0003t0003g0285a0001c0008t0003g0276others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-17322A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718936 | ||||||
| chr4:140719115
|
A | AAAAT | 23 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0149others(20): Show | 23 | HG00673.hp1 HG01106.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-17505_131-1750 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719115
|
A | AAAATAAA others(1): Show |
7 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0165others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-17509_131-1750 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719115
|
AAAAT | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 38 | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.131-17505_131-1750 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719115
|
AAAATAAA others(1): Show |
A | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.131-17509_131-1750 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719115
|
AAAATAAA others(5): Show |
A | 3 | a0001c0006t0001g0205a0001c0008t0001g0185a0001c0008t0002g0186 | 3 | HG02647.hp2 HG03139.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.131-17513_131-1750 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719115
|
AAAATAAA others(9): Show |
A | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-17517_131-1750 others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719115
|
AAAATAAA others(21): Show |
A | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-17529_131-1750 others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | ||||||
| chr4:140719139
|
T | C | 2 | a0001c0002t0001g0226a0001c0006t0001g0257 | 2 | NA18967.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.131-17525A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719139 | ||||||
| chr4:140719161
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0191 | 2 | HG00544.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.131-17547T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719161 | ||||||
| chr4:140719359
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-17745G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719359 | ||||||
| chr4:140719419
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.131-17805C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719419 | ||||||
| chr4:140719590
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.131-17976A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719590 | ||||||
| chr4:140719685
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0004g0292 | 3 | NA18948.hp2 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.131-18071A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719685 | ||||||
| chr4:140720070
|
T | C | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131-18456A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720070 | ||||||
| chr4:140720094
|
T | G | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-18480A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720094 | ||||||
| chr4:140720283
|
A | G | 14 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(11): Show | 14 | HG00733.hp1 HG01257.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-18669T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720283 | ||||||
| chr4:140720375
|
A | C | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-18761T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720375 | ||||||
| chr4:140720577
|
G | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.131-18963C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720577 | ||||||
| chr4:140720699
|
G | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.131-19085C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720699 | ||||||
| chr4:140720787
|
C | G | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-19173G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720787 | ||||||
| chr4:140720908
|
T | C | 1 | a0001c0002t0001g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.131-19294A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720908 | ||||||
| chr4:140721049
|
G | A | 3 | a0001c0002t0001g0215a0001c0002t0001g0226a0001c0006t0001g0257 | 3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.131-19435C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721049 | ||||||
| chr4:140721062
|
C | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.131-19448G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721062 | ||||||
| chr4:140721272
|
A | G | 1 | a0001c0001t0003g0278 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.131-19658T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721272 | ||||||
| chr4:140721692
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(127): Show | 131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.131-20078G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721692 | ||||||
| chr4:140721765
|
C | T | 130 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0090others(127): Show | 131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.131-20151G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721765 | ||||||
| chr4:140721966
|
C | T | 7 | a0001c0001t0002g0182a0001c0002t0001g0195a0001c0002t0001g0245others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-20352G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721966 | ||||||
| chr4:140722005
|
T | C | 3 | a0001c0002t0003g0281a0001c0002t0003g0283a0001c0002t0003g0290 | 3 | HG01074.hp2 HG01361.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.131-20391A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722005 | ||||||
| chr4:140722096
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-20482A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722096 | ||||||
| chr4:140722273
|
G | GA | 7 | a0001c0001t0001g0134a0001c0001t0002g0274a0001c0002t0002g0087others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-20660dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722273 | ||||||
| chr4:140722341
|
C | T | 21 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-20727G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722341 | ||||||
| chr4:140722518
|
G | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-20904C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722518 | ||||||
| chr4:140722534
|
T | C | 5 | a0001c0001t0002g0182a0001c0008t0001g0183a0001c0008t0001g0185others(2): Show | 5 | HG02451.hp2 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-20920A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722534 | ||||||
| chr4:140722591
|
T | C | 1 | a0001c0003t0001g0068 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.131-20977A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722591 | ||||||
| chr4:140722657
|
G | T | 1 | a0001c0005t0002g0127 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.131-21043C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722657 | ||||||
| chr4:140722866
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-21252C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722866 | ||||||
| chr4:140722888
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.131-21274A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722888 | ||||||
| chr4:140722906
|
C | T | 4 | a0001c0001t0014g0284a0001c0003t0003g0285a0001c0004t0001g0086others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-21292G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722906 | ||||||
| chr4:140723218
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0017g0297 | 3 | HG02258.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.131-21604G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723218 | ||||||
| chr4:140723220
|
T | C | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-21606A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723220 | ||||||
| chr4:140723326
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131-21712G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723326 | ||||||
| chr4:140723375
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.131-21761C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723375 | ||||||
| chr4:140723754
|
T | G | 4 | a0001c0004t0005g0265a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-22140A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723754 | ||||||
| chr4:140723900
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-22286C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723900 | ||||||
| chr4:140724154
|
G | A | 18 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-22540C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724154 | ||||||
| chr4:140724497
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.131-22883G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724497 | ||||||
| chr4:140724530
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-22916G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724530 | ||||||
| chr4:140724640
|
GA | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0082others(3): Show | 6 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23027delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724640 | ||||||
| chr4:140724716
|
T | C | 1 | a0001c0007t0001g0238 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.131-23102A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724716 | ||||||
| chr4:140724802
|
A | T | 1 | a0003c0019t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.131-23188T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724802 | ||||||
| chr4:140725069
|
C | T | 1 | a0001c0003t0001g0040 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.131-23455G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725069 | ||||||
| chr4:140725123
|
C | T | 2 | a0001c0002t0003g0281a0001c0002t0003g0290 | 2 | HG01074.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.131-23509G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725123 | ||||||
| chr4:140725179
|
T | A | 18 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-23565A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725179 | ||||||
| chr4:140725284
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0248a0001c0002t0001g0189others(3): Show | 6 | NA18941.hp2 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23670C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725284 | ||||||
| chr4:140725446
|
T | G | 4 | a0001c0001t0002g0043a0001c0001t0010g0054a0001c0003t0001g0055others(1): Show | 4 | HG02155.hp1 NA18991.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-23832A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725446 | ||||||
| chr4:140725688
|
T | G | 21 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-24074A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725688 | ||||||
| chr4:140725718
|
T | C | 4 | a0001c0005t0001g0128a0001c0005t0001g0129a0001c0005t0002g0127others(1): Show | 4 | HG00639.hp1 HG02300.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-24104A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725718 | ||||||
| chr4:140726106
|
T | C | 8 | a0001c0003t0001g0096a0001c0005t0001g0128a0001c0005t0001g0129others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-24492A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726106 | ||||||
| chr4:140726247
|
C | T | 1 | a0003c0019t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.131-24633G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726247 | ||||||
| chr4:140726302
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-24688A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726302 | ||||||
| chr4:140726306
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02630.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-24692T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726306 | ||||||
| chr4:140726366
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-24752A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726366 | ||||||
| chr4:140726513
|
A | C | 2 | a0001c0002t0001g0137a0001c0004t0001g0136 | 2 | HG01928.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.131-24899T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726513 | ||||||
| chr4:140726574
|
C | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.131-24960G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726574 | ||||||
| chr4:140726724
|
C | T | 1 | a0001c0003t0001g0030 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.131-25110G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726724 | ||||||
| chr4:140726725
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.131-25111C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726725 | ||||||
| chr4:140726735
|
G | T | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-25121C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726735 | ||||||
| chr4:140726946
|
C | T | 18 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-25332G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726946 | ||||||
| chr4:140727130
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.131-25516A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727130 | ||||||
| chr4:140727291
|
C | A | 4 | a0001c0002t0001g0244a0001c0002t0001g0267a0001c0002t0001g0268others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-25677G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727291 | ||||||
| chr4:140727541
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-25927G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727541 | ||||||
| chr4:140727739
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-26125A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727739 | ||||||
| chr4:140727789
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-26175G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727789 | ||||||
| chr4:140727832
|
A | G | 1 | a0001c0002t0015g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-26218T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727832 | ||||||
| chr4:140728280
|
A | C | 2 | a0001c0002t0001g0196a0001c0002t0001g0246 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.131-26666T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728280 | ||||||
| chr4:140728323
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0004t0005g0265others(4): Show | 7 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-26709A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728323 | ||||||
| chr4:140728401
|
TA | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.131-26788delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728401 | ||||||
| chr4:140728493
|
T | C | 1 | a0001c0004t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.131-26879A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728493 | ||||||
| chr4:140728619
|
G | C | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.131-27005C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728619 | ||||||
| chr4:140728701
|
C | T | 4 | a0001c0004t0005g0265a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-27087G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728701 | ||||||
| chr4:140729091
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.130+26825A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729091 | ||||||
| chr4:140729117
|
C | T | 18 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+26799G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729117 | ||||||
| chr4:140729122
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.130+26794G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729122 | ||||||
| chr4:140729131
|
C | A | 2 | a0001c0002t0001g0180a0001c0002t0001g0242 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.130+26785G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729131 | ||||||
| chr4:140729272
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+26644A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729272 | ||||||
| chr4:140729418
|
C | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+26498G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729418 | ||||||
| chr4:140729436
|
T | A | 12 | a0001c0001t0001g0217a0001c0002t0001g0223a0001c0003t0001g0216others(9): Show | 12 | HG02083.hp2 HG02165.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+26480A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729436 | ||||||
| chr4:140729442
|
C | T | 3 | a0001c0002t0001g0244a0001c0002t0001g0267a0001c0002t0001g0268 | 3 | HG02896.hp1 HG02897.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.130+26474G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729442 | ||||||
| chr4:140729446
|
A | G | 7 | a0001c0001t0001g0134a0001c0001t0002g0274a0001c0002t0002g0087others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+26470T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729446 | ||||||
| chr4:140729487
|
C | G | 3 | a0001c0001t0001g0194a0001c0002t0001g0064a0001c0003t0007g0012 | 3 | NA18964.hp2 NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.130+26429G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729487 | ||||||
| chr4:140729647
|
G | A | 1 | a0001c0001t0003g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.130+26269C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729647 | ||||||
| chr4:140729693
|
G | A | 1 | a0001c0008t0002g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.130+26223C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729693 | ||||||
| chr4:140729697
|
G | A | 2 | a0001c0008t0001g0179a0001c0008t0005g0178 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.130+26219C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729697 | ||||||
| chr4:140729818
|
C | CA | 21 | a0001c0001t0001g0122a0001c0001t0001g0163a0001c0001t0001g0165others(18): Show | 21 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+26097dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729818
|
C | CAA | 84 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0092others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.130+26096_130+2609 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729818
|
C | CAAA | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.130+26095_130+2609 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729818
|
C | CAAAA | 22 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0019others(19): Show | 22 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.130+26094_130+2609 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729818
|
CA | C | 10 | a0001c0001t0001g0116a0001c0001t0003g0277a0001c0002t0001g0244others(7): Show | 10 | HG00099.hp1 HG00639.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+26097delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729818
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0014g0284a0001c0003t0003g0285a0001c0004t0001g0086others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+26087_130+2609 others(15): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729818
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0002g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.130+26085_130+2609 others(17): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | ||||||
| chr4:140729875
|
G | T | 6 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+26041C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729875 | ||||||
| chr4:140730280
|
G | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.130+25636C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730280 | ||||||
| chr4:140730438
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.130+25478G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730438 | ||||||
| chr4:140730572
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+25344G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730572 | ||||||
| chr4:140730664
|
T | C | 1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+25252A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730664 | ||||||
| chr4:140730703
|
G | T | 13 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0248others(10): Show | 13 | HG01346.hp2 HG01975.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+25213C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730703 | ||||||
| chr4:140730722
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.130+25194A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730722 | ||||||
| chr4:140730727
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+25189T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730727 | ||||||
| chr4:140730944
|
G | A | 1 | a0001c0002t0001g0234 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.130+24972C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730944 | ||||||
| chr4:140731026
|
T | A | 2 | a0001c0002t0002g0225a0001c0002t0002g0231 | 2 | HG01346.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.130+24890A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731026 | ||||||
| chr4:140731150
|
T | C | 1 | a0001c0005t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+24766A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731150 | ||||||
| chr4:140731206
|
C | T | 4 | a0001c0004t0005g0265a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24710G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731206 | ||||||
| chr4:140731214
|
T | C | 2 | a0001c0005t0001g0145a0001c0005t0001g0157 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.130+24702A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731214 | ||||||
| chr4:140731360
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0163 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.130+24556A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731360 | ||||||
| chr4:140731376
|
T | C | 4 | a0001c0004t0005g0265a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24540A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731376 | ||||||
| chr4:140731503
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.130+24413G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731503 | ||||||
| chr4:140731605
|
T | C | 4 | a0001c0001t0014g0284a0001c0003t0003g0285a0001c0004t0001g0086others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24311A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731605 | ||||||
| chr4:140731668
|
T | C | 4 | a0001c0004t0005g0265a0001c0008t0001g0240a0001c0008t0005g0241others(1): Show | 4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24248A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731668 | ||||||
| chr4:140731668
|
T | TAC | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.130+24246_130+2424 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731668 | ||||||
| chr4:140731693
|
A | C | 26 | a0001c0001t0001g0143a0001c0001t0001g0160a0001c0001t0001g0161others(23): Show | 26 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.130+24223T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731693 | ||||||
| chr4:140731694
|
C | CAT | 18 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+24221_130+2422 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731694 | ||||||
| chr4:140731757
|
G | C | 2 | a0001c0020t0001g0187a0001c0021t0001g0264 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130+24159C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731757 | ||||||
| chr4:140731768
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.130+24148T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731768 | ||||||
| chr4:140731852
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130+24064A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731852 | ||||||
| chr4:140731899
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.130+24017A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731899 | ||||||
| chr4:140731901
|
T | C | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.130+24015A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731901 | ||||||
| chr4:140732078
|
G | A | 5 | a0001c0001t0014g0284a0001c0003t0003g0285a0001c0004t0001g0086others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+23838C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732078 | ||||||
| chr4:140732114
|
T | C | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+23802A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732114 | ||||||
| chr4:140732166
|
G | T | 8 | a0001c0003t0001g0096a0001c0005t0001g0128a0001c0005t0001g0129others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+23750C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732166 | ||||||
| chr4:140732185
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+23731C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732185 | ||||||
| chr4:140732243
|
A | G | 6 | a0001c0004t0001g0045a0002c0009t0002g0036a0002c0009t0002g0039others(3): Show | 6 | NA18966.hp1 NA18982.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+23673T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732243 | ||||||
| chr4:140732377
|
T | C | 1 | a0001c0016t0012g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130+23539A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732377 | ||||||
| chr4:140732414
|
C | A | 1 | a0001c0002t0001g0199 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.130+23502G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732414 | ||||||
| chr4:140733155
|
C | G | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+22761G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733155 | ||||||
| chr4:140733297
|
A | AT | 8 | a0001c0003t0001g0096a0001c0005t0001g0128a0001c0005t0001g0129others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+22618dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733297 | ||||||
| chr4:140733418
|
T | A | 1 | a0001c0002t0001g0226 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.130+22498A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733418 | ||||||
| chr4:140733484
|
T | C | 9 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0002t0001g0188others(6): Show | 9 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+22432A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733484 | ||||||
| chr4:140733687
|
G | A | 1 | a0001c0001t0004g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.130+22229C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733687 | ||||||
| chr4:140733754
|
C | A | 1 | a0001c0006t0007g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.130+22162G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733754 | ||||||
| chr4:140734022
|
A | G | 80 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0184others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.130+21894T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734022 | ||||||
| chr4:140734292
|
C | T | 2 | a0001c0004t0001g0228a0001c0004t0002g0260 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.130+21624G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734292 | ||||||
| chr4:140734326
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(128): Show | 132 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.130+21590G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734326 | ||||||
| chr4:140734327
|
G | A | 7 | a0001c0001t0001g0134a0001c0001t0002g0274a0001c0002t0002g0087others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+21589C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734327 | ||||||
| chr4:140734377
|
A | G | 7 | a0001c0001t0001g0134a0001c0001t0002g0274a0001c0002t0002g0087others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+21539T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734377 | ||||||
| chr4:140734520
|
G | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.130+21396C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734520 | ||||||
| chr4:140734565
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0004t0005g0265others(2): Show | 5 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+21351C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734565 | ||||||
| chr4:140734636
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.130+21280T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734636 | ||||||
| chr4:140734638
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+21278A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734638 | ||||||
| chr4:140734827
|
A | G | 1 | a0001c0004t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.130+21089T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734827 | ||||||
| chr4:140735191
|
T | C | 104 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0143others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.130+20725A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735191 | ||||||
| chr4:140735256
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+20660T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735256 | ||||||
| chr4:140735313
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.130+20603C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735313 | ||||||
| chr4:140735436
|
G | A | 1 | a0001c0010t0001g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.130+20480C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735436 | ||||||
| chr4:140735449
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+20467G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735449 | ||||||
| chr4:140735619
|
G | A | 1 | a0001c0013t0011g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+20297C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735619 | ||||||
| chr4:140735683
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0010 | 2 | NA18972.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.130+20233G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735683 | ||||||
| chr4:140735907
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+20009G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735907 | ||||||
| chr4:140735930
|
T | C | 2 | a0001c0002t0002g0087a0001c0004t0001g0086 | 2 | HG00639.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.130+19986A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735930 | ||||||
| chr4:140736065
|
C | T | 1 | a0001c0008t0001g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130+19851G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736065 | ||||||
| chr4:140736163
|
G | GGGAGAGA others(11): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0191a0001c0003t0001g0085 | 3 | HG00544.hp2 NA18982.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.130+19735_130+1975 others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736163 | ||||||
| chr4:140736350
|
G | A | 6 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+19566C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736350 | ||||||
| chr4:140736366
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.130+19550G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736366 | ||||||
| chr4:140736465
|
C | T | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.130+19451G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736465 | ||||||
| chr4:140736499
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.130+19417G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736499 | ||||||
| chr4:140736933
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+18983A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736933 | ||||||
| chr4:140737070
|
A | C | 1 | a0001c0004t0005g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+18846T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737070 | ||||||
| chr4:140737121
|
G | A | 130 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0090others(127): Show | 131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.130+18795C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737121 | ||||||
| chr4:140737436
|
TTC | T | 9 | a0001c0001t0001g0023a0001c0002t0001g0244a0001c0002t0001g0267others(6): Show | 9 | HG01167.hp2 HG01261.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+18478_130+1847 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | ||||||
| chr4:140737436
|
TTCTC | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.130+18476_130+1847 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | ||||||
| chr4:140737436
|
TTCTCTC | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(122): Show | 126 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.130+18474_130+1847 others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | ||||||
| chr4:140737436
|
TTCTCTCT others(1): Show |
T | 9 | a0001c0002t0001g0098a0001c0003t0001g0096a0001c0005t0001g0128others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+18472_130+1847 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | ||||||
| chr4:140737436
|
TTCTCTCT others(3): Show |
T | 4 | a0001c0001t0001g0090a0001c0001t0001g0147a0001c0002t0001g0230others(1): Show | 4 | HG01891.hp1 NA18953.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+18470_130+1847 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | ||||||
| chr4:140737465
|
T | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0134others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+18451A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737465 | ||||||
| chr4:140737543
|
T | C | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.130+18373A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737543 | ||||||
| chr4:140737723
|
C | A | 2 | a0001c0008t0001g0240a0001c0008t0005g0241 | 2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130+18193G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737723 | ||||||
| chr4:140738154
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+17762G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738154 | ||||||
| chr4:140738336
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+17580G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738336 | ||||||
| chr4:140738435
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.130+17481A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738435 | ||||||
| chr4:140738485
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+17431G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738485 | ||||||
| chr4:140738699
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0004t0005g0265others(2): Show | 5 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+17217G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738699 | ||||||
| chr4:140738875
|
T | A | 3 | a0001c0002t0001g0244a0001c0002t0001g0267a0001c0002t0001g0268 | 3 | HG02896.hp1 HG02897.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.130+17041A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738875 | ||||||
| chr4:140738952
|
G | A | 6 | a0001c0004t0001g0045a0002c0009t0002g0036a0002c0009t0002g0039others(3): Show | 6 | NA18966.hp1 NA18982.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+16964C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738952 | ||||||
| chr4:140739047
|
TTGCTGCC others(95): Show |
T | 1 | a0001c0005t0001g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.130+16767_130+1686 others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739047 | ||||||
| chr4:140739074
|
G | A | 2 | a0001c0002t0001g0195a0001c0002t0001g0245 | 2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.130+16842C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739074 | ||||||
| chr4:140739118
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+16798A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739118 | ||||||
| chr4:140739141
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0248a0001c0002t0001g0189others(3): Show | 6 | NA18941.hp2 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+16775G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739141 | ||||||
| chr4:140739173
|
T | C | 130 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0090others(127): Show | 131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.130+16743A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739173 | ||||||
| chr4:140739192
|
A | G | 1 | a0001c0003t0001g0071 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.130+16724T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739192 | ||||||
| chr4:140739273
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+16643G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739273 | ||||||
| chr4:140739277
|
C | T | 17 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(14): Show | 17 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+16639G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739277 | ||||||
| chr4:140739425
|
C | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01517.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+16491G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739425 | ||||||
| chr4:140739466
|
G | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.130+16450C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739466 | ||||||
| chr4:140739834
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.130+16082A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739834 | ||||||
| chr4:140739848
|
A | T | 2 | a0001c0005t0002g0101a0001c0005t0002g0102 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.130+16068T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739848 | ||||||
| chr4:140739884
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.130+16032T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739884 | ||||||
| chr4:140739971
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+15945A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739971 | ||||||
| chr4:140740195
|
T | C | 17 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(14): Show | 17 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+15721A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740195 | ||||||
| chr4:140740533
|
A | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+15383T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740533 | ||||||
| chr4:140740585
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0004t0005g0265others(2): Show | 5 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+15331C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740585 | ||||||
| chr4:140740833
|
G | A | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+15083C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740833 | ||||||
| chr4:140740920
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.130+14996A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740920 | ||||||
| chr4:140741009
|
T | C | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0143others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.130+14907A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741009 | ||||||
| chr4:140741124
|
C | T | 17 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(14): Show | 17 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+14792G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741124 | ||||||
| chr4:140741155
|
A | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+14761T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741155 | ||||||
| chr4:140741362
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.130+14554T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741362 | ||||||
| chr4:140741442
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0002g0105a0001c0003t0001g0021others(1): Show | 4 | HG01167.hp2 HG01943.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+14474A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741442 | ||||||
| chr4:140741524
|
C | T | 2 | a0001c0002t0001g0094a0001c0010t0001g0190 | 2 | NA19056.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.130+14392G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741524 | ||||||
| chr4:140741932
|
G | A | 2 | a0001c0001t0001g0025a0001c0003t0001g0024 | 2 | NA18970.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.130+13984C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741932 | ||||||
| chr4:140741991
|
G | T | 9 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0002t0001g0188others(6): Show | 9 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+13925C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741991 | ||||||
| chr4:140742179
|
A | G | 1 | a0001c0002t0001g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+13737T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742179 | ||||||
| chr4:140742247
|
T | C | 4 | a0001c0001t0014g0284a0001c0003t0003g0285a0001c0004t0001g0086others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+13669A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742247 | ||||||
| chr4:140742255
|
C | T | 19 | a0001c0001t0001g0044a0001c0001t0001g0076a0001c0001t0001g0079others(16): Show | 19 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+13661G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742255 | ||||||
| chr4:140742323
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130+13593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742323 | ||||||
| chr4:140742442
|
T | A | 4 | a0001c0001t0001g0072a0001c0003t0001g0071a0001c0003t0001g0073others(1): Show | 4 | HG00408.hp1 HG00673.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+13474A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742442 | ||||||
| chr4:140742531
|
C | CA | 15 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0002g0274others(12): Show | 15 | HG00639.hp2 HG02056.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+13384dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | ||||||
| chr4:140742531
|
CA | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 102 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.130+13384delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | ||||||
| chr4:140742531
|
CAA | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(15): Show | 18 | HG01106.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.130+13383_130+1338 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | ||||||
| chr4:140742531
|
CAAA | C | 93 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0143others(90): Show | 94 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+13382_130+1338 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | ||||||
| chr4:140742635
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+13281A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742635 | ||||||
| chr4:140742888
|
CAGG | C | 74 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0184others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.130+13025_130+1302 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742888 | ||||||
| chr4:140742902
|
G | A | 4 | a0001c0001t0002g0089a0001c0001t0002g0156a0001c0005t0001g0145others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+13014C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742902 | ||||||
| chr4:140742977
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.130+12939C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742977 | ||||||
| chr4:140743038
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.130+12878C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743038 | ||||||
| chr4:140743365
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.130+12551G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743365 | ||||||
| chr4:140743574
|
G | C | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+12342C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743574 | ||||||
| chr4:140743583
|
T | C | 2 | a0001c0001t0002g0274a0001c0005t0001g0171 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+12333A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743583 | ||||||
| chr4:140743634
|
G | C | 1 | a0001c0001t0002g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.130+12282C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743634 | ||||||
| chr4:140743682
|
C | T | 1 | a0001c0003t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.130+12234G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743682 | ||||||
| chr4:140743684
|
G | T | 1 | a0001c0004t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+12232C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743684 | ||||||
| chr4:140743707
|
A | G | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+12209T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743707 | ||||||
| chr4:140743743
|
C | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+12173G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743743 | ||||||
| chr4:140743914
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+12002G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743914 | ||||||
| chr4:140743935
|
T | G | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+11981A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743935 | ||||||
| chr4:140744036
|
G | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0057others(123): Show | 127 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.130+11880C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744036 | ||||||
| chr4:140744133
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.130+11783C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744133 | ||||||
| chr4:140744175
|
T | C | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+11741A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744175 | ||||||
| chr4:140744286
|
A | C | 3 | a0001c0008t0001g0179a0001c0008t0005g0178a0001c0018t0001g0174 | 3 | HG02280.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.130+11630T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744286 | ||||||
| chr4:140744305
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0002g0243 | 2 | HG00733.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.130+11611G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744305 | ||||||
| chr4:140744333
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.130+11583T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744333 | ||||||
| chr4:140744357
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+11559T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744357 | ||||||
| chr4:140744423
|
T | G | 5 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0100others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+11493A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744423 | ||||||
| chr4:140744504
|
G | C | 83 | a0001c0001t0001g0033a0001c0001t0001g0184a0001c0001t0001g0191others(80): Show | 84 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.130+11412C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744504 | ||||||
| chr4:140744693
|
G | A | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+11223C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744693 | ||||||
| chr4:140744798
|
G | A | 2 | a0001c0001t0001g0002a0001c0004t0001g0086 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130+11118C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744798 | ||||||
| chr4:140744879
|
T | TA | 10 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0016g0295others(7): Show | 10 | HG00639.hp2 HG00735.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+11036dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744879
|
TA | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.130+11036delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744879
|
TAA | T | 91 | a0001c0001t0001g0076a0001c0001t0001g0143a0001c0001t0001g0144others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.130+11035_130+1103 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744879
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+11027_130+1103 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744879
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0002t0001g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.130+11026_130+1103 others(15): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744879
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+11025_130+1103 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744879
|
TAAAAAAA others(7): Show |
T | 2 | a0001c0004t0005g0265a0001c0013t0011g0115 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.130+11023_130+1103 others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | ||||||
| chr4:140744925
|
C | A | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+10991G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744925 | ||||||
| chr4:140744926
|
C | T | 1 | a0001c0008t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+10990G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744926 | ||||||
| chr4:140744954
|
T | G | 1 | a0001c0006t0001g0235 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.130+10962A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744954 | ||||||
| chr4:140744967
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+10949A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744967 | ||||||
| chr4:140745018
|
C | A | 3 | a0001c0001t0001g0134a0001c0002t0002g0087a0001c0014t0001g0088 | 3 | HG00639.hp2 HG01361.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.130+10898G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745018 | ||||||
| chr4:140745096
|
T | C | 1 | a0001c0003t0001g0030 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.130+10820A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745096 | ||||||
| chr4:140745105
|
A | T | 12 | a0001c0001t0001g0134a0001c0001t0002g0274a0001c0002t0002g0087others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+10811T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745105 | ||||||
| chr4:140745196
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0002t0001g0097others(5): Show | 8 | HG00735.hp1 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+10720A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745196 | ||||||
| chr4:140745339
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.130+10577A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745339 | ||||||
| chr4:140745498
|
T | C | 1 | a0001c0003t0001g0096 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.130+10418A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745498 | ||||||
| chr4:140745504
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+10412G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745504 | ||||||
| chr4:140745553
|
T | C | 2 | a0001c0008t0001g0185a0001c0008t0002g0186 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.130+10363A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745553 | ||||||
| chr4:140745594
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.130+10322A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745594 | ||||||
| chr4:140745789
|
T | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(65): Show | 68 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.130+10127A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745789 | ||||||
| chr4:140745839
|
C | T | 1 | a0001c0004t0005g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+10077G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745839 | ||||||
| chr4:140745988
|
G | A | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+9928C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745988 | ||||||
| chr4:140746109
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.130+9807G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746109 | ||||||
| chr4:140746207
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.130+9709C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746207 | ||||||
| chr4:140746420
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.130+9496T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746420 | ||||||
| chr4:140746500
|
G | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0075 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.130+9416C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746500 | ||||||
| chr4:140746637
|
C | T | 2 | a0001c0005t0002g0101a0001c0005t0002g0102 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.130+9279G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746637 | ||||||
| chr4:140746725
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG03491.hp2 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.130+9191A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746725 | ||||||
| chr4:140746888
|
C | T | 2 | a0001c0001t0002g0182a0001c0004t0001g0142 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.130+9028G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746888 | ||||||
| chr4:140746891
|
G | A | 3 | a0001c0004t0005g0265a0001c0008t0001g0240a0001c0008t0005g0241 | 3 | HG01261.hp2 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130+9025C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746891 | ||||||
| chr4:140746926
|
G | T | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+8990C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746926 | ||||||
| chr4:140747017
|
A | AAAAT | 14 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0001g0266others(11): Show | 14 | HG00639.hp1 HG00735.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+8895_130+8898d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747017 | ||||||
| chr4:140747017
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+8899T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747017 | ||||||
| chr4:140747021
|
T | A | 39 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0112others(36): Show | 39 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.130+8895A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747021 | ||||||
| chr4:140747042
|
G | A | 1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+8874C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747042 | ||||||
| chr4:140747164
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.130+8752C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747164 | ||||||
| chr4:140747349
|
C | CA | 87 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0191others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.130+8566dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747349 | ||||||
| chr4:140747393
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.130+8523G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747393 | ||||||
| chr4:140747473
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130+8443T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747473 | ||||||
| chr4:140747501
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+8415C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747501 | ||||||
| chr4:140747517
|
A | G | 85 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0191others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.130+8399T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747517 | ||||||
| chr4:140747590
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.130+8326A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747590 | ||||||
| chr4:140747613
|
G | A | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+8303C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747613 | ||||||
| chr4:140747735
|
T | TA | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0169others(5): Show | 8 | HG00408.hp2 NA18944.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+8180_130+8181i others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747735 | ||||||
| chr4:140747743
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130+8173G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747743 | ||||||
| chr4:140747749
|
T | C | 2 | a0001c0002t0001g0180a0001c0002t0001g0242 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.130+8167A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747749 | ||||||
| chr4:140748184
|
A | C | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+7732T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748184 | ||||||
| chr4:140748469
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.130+7447C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748469 | ||||||
| chr4:140748533
|
G | C | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+7383C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748533 | ||||||
| chr4:140748653
|
A | G | 1 | a0001c0004t0005g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+7263T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748653 | ||||||
| chr4:140748654
|
C | T | 2 | a0001c0002t0001g0094a0001c0010t0001g0190 | 2 | NA19056.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.130+7262G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748654 | ||||||
| chr4:140748730
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.130+7186T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748730 | ||||||
| chr4:140748942
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0061 | 2 | HG00733.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.130+6974C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748942 | ||||||
| chr4:140748989
|
G | A | 1 | a0001c0001t0017g0297 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+6927C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748989 | ||||||
| chr4:140749073
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.130+6843A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749073 | ||||||
| chr4:140749116
|
A | G | 1 | a0001c0004t0005g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+6800T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749116 | ||||||
| chr4:140749253
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+6663C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749253 | ||||||
| chr4:140749272
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+6644A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749272 | ||||||
| chr4:140749601
|
T | C | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.130+6315A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749601 | ||||||
| chr4:140749651
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130+6265G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749651 | ||||||
| chr4:140749674
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+6242A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749674 | ||||||
| chr4:140749717
|
C | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.130+6199G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749717 | ||||||
| chr4:140749745
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034 | 3 | HG01255.hp2 HG02004.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.130+6171T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749745 | ||||||
| chr4:140749866
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130+6050A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749866 | ||||||
| chr4:140749980
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+5936A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749980 | ||||||
| chr4:140750080
|
G | A | 4 | a0001c0004t0001g0123a0001c0004t0001g0125a0001c0004t0002g0126others(1): Show | 4 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+5836C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750080 | ||||||
| chr4:140750119
|
A | T | 1 | a0001c0001t0006g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.130+5797T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750119 | ||||||
| chr4:140750159
|
T | A | 1 | a0001c0002t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.130+5757A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750159 | ||||||
| chr4:140750159
|
T | TA | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.130+5756dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750159 | ||||||
| chr4:140750172
|
T | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0002t0002g0091 | 3 | HG02615.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.130+5744A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750172 | ||||||
| chr4:140750235
|
G | T | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130+5681C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750235 | ||||||
| chr4:140750419
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.130+5497G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750419 | ||||||
| chr4:140750493
|
A | G | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.130+5423T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750493 | ||||||
| chr4:140750624
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0001g0184others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.130+5292C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750624 | ||||||
| chr4:140750692
|
C | T | 1 | a0001c0004t0001g0086 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+5224G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750692 | ||||||
| chr4:140750795
|
T | C | 30 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(27): Show | 30 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+5121A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750795 | ||||||
| chr4:140750806
|
TGCAAGCT others(13): Show |
T | 1 | a0001c0001t0001g0007 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.130+5090_130+5109d others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750806 | ||||||
| chr4:140750975
|
T | TA | 12 | a0001c0001t0001g0134a0001c0001t0002g0274a0001c0002t0002g0087others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+4940dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750975 | ||||||
| chr4:140751349
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.130+4567T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751349 | ||||||
| chr4:140751494
|
T | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.130+4422A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751494 | ||||||
| chr4:140751533
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+4383A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751533 | ||||||
| chr4:140751641
|
C | T | 2 | a0001c0002t0001g0180a0001c0002t0001g0242 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.130+4275G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751641 | ||||||
| chr4:140751760
|
T | C | 1 | a0001c0020t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+4156A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751760 | ||||||
| chr4:140751775
|
G | A | 5 | a0001c0002t0001g0137a0001c0002t0001g0173a0001c0004t0001g0135others(2): Show | 5 | HG00741.hp1 HG01256.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+4141C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751775 | ||||||
| chr4:140751947
|
T | C | 1 | a0001c0014t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.130+3969A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751947 | ||||||
| chr4:140752057
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0001g0181others(90): Show | 94 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+3859G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752057 | ||||||
| chr4:140752129
|
C | A | 1 | a0001c0004t0001g0272 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130+3787G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752129 | ||||||
| chr4:140752193
|
G | T | 1 | a0001c0002t0001g0173 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130+3723C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752193 | ||||||
| chr4:140752360
|
TA | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0163a0001c0001t0001g0181others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.130+3555delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752360 | ||||||
| chr4:140752442
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.130+3474G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752442 | ||||||
| chr4:140752566
|
T | TA | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.130+3349dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752566 | ||||||
| chr4:140752838
|
C | G | 30 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(27): Show | 30 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+3078G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752838 | ||||||
| chr4:140752902
|
A | G | 2 | a0001c0001t0002g0089a0001c0003t0001g0096 | 2 | HG00099.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.130+3014T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752902 | ||||||
| chr4:140752920
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 5 | HG00621.hp2 HG02056.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+2996C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752920 | ||||||
| chr4:140753037
|
C | T | 1 | a0001c0002t0003g0275 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130+2879G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753037 | ||||||
| chr4:140753040
|
A | T | 1 | a0001c0018t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130+2876T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753040 | ||||||
| chr4:140753070
|
G | C | 1 | a0001c0001t0004g0296 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.130+2846C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753070 | ||||||
| chr4:140753086
|
G | C | 1 | a0001c0021t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+2830C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753086 | ||||||
| chr4:140753295
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+2621A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753295 | ||||||
| chr4:140753307
|
C | T | 85 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0191others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.130+2609G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753307 | ||||||
| chr4:140753388
|
C | G | 1 | a0001c0005t0009g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+2528G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753388 | ||||||
| chr4:140753447
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+2469C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753447 | ||||||
| chr4:140753535
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+2381T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753535 | ||||||
| chr4:140753675
|
T | C | 1 | a0001c0003t0001g0239 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130+2241A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753675 | ||||||
| chr4:140753893
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130+2023C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753893 | ||||||
| chr4:140754046
|
T | C | 59 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(56): Show | 59 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.130+1870A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754046 | ||||||
| chr4:140754388
|
C | T | 59 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(56): Show | 59 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.130+1528G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754388 | ||||||
| chr4:140754545
|
A | C | 1 | a0001c0002t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.130+1371T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754545 | ||||||
| chr4:140754604
|
G | A | 59 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(56): Show | 59 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.130+1312C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754604 | ||||||
| chr4:140754614
|
C | CA | 56 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0072others(53): Show | 56 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.130+1301dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | ||||||
| chr4:140754614
|
C | CAA | 14 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0002g0182others(11): Show | 14 | HG01515.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.130+1300_130+1301d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | ||||||
| chr4:140754614
|
C | CAAA | 55 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0198others(52): Show | 56 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.130+1299_130+1301d others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | ||||||
| chr4:140754614
|
C | CAAAA | 24 | a0001c0001t0001g0248a0001c0001t0001g0251a0001c0001t0001g0256others(21): Show | 24 | HG01167.hp1 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.130+1298_130+1301d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | ||||||
| chr4:140754614
|
CA | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0092others(8): Show | 11 | HG00639.hp2 HG01361.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+1301delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | ||||||
| chr4:140754804
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.130+1112C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754804 | ||||||
| chr4:140754936
|
C | A | 6 | a0001c0001t0001g0270a0001c0001t0002g0269a0001c0002t0001g0267others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+980G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754936 | ||||||
| chr4:140755501
|
C | A | 1 | a0001c0003t0001g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.130+415G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755501 | ||||||
| chr4:140755507
|
C | A | 22 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0279others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+409G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755507 | ||||||
| chr4:140755755
|
A | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.130+161T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755755 | ||||||
| chr4:140755817
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130+99T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755817 | ||||||
| chr4:140755838
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+78G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755838 | ||||||
| chr4:140755852
|
A | AG | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.130+63dupC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755852 | ||||||
| chr4:140755901
|
G | C | 1 | a0001c0001t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+15C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755901 |