Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55296 |
| ensemblid | ENSG00000109680.11 |
| hgncid | 25624 |
| symbol | TBC1D19 |
| name | TBC1 domain family member 19 |
| refseq_nuc | NM_018317.4 |
| refseq_prot | NP_060787.2 |
| ensembl_nuc | ENST00000264866.9 |
| ensembl_prot | ENSP00000264866.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 26584084 |
| end | 26756223 |
| strand | + |
| ver | v1.2 |
| region | chr4:26584084-26756223 |
| region5000 | chr4:26579084-26761223 |
| regionname0 | TBC1D19_chr4_26584084_26756223 |
| regionname5000 | TBC1D19_chr4_26579084_26761223 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 526 | 303 | 87 | 43 | 131 | 12 | 28 | 107 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | MLQEE others(521): Show |
chr4 | 26579084 | 26761223 |
| a0002 | 0/0 | 526 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | MLQEE others(521): Show |
chr4 | 26579084 | 26761223 |
| a0003 | 0/0 | 526 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | MLQEE others(521): Show |
chr4 | 26579084 | 26761223 |
| a0004 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | MLQEE others(521): Show |
chr4 | 26579084 | 26761223 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1578 | 172 | 55 | 25 | 74 | 5 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0001c0002 | 0/0 | 1578 | 104 | 19 | 16 | 51 | 6 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0001c0003 | 0/0 | 1578 | 8 | 1 | 0 | 5 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0001c0004 | 1/0 | 1578 | 7 | 6 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0001c0005 | 0/0 | 1578 | 7 | 1 | 2 | 1 | 1 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0001c0006 | 0/0 | 1578 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0001c0010 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0002c0007 | 0/0 | 1578 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0003c0008 | 0/0 | 1578 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 | ||
| a0004c0009 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | ATGTT others(1573): Show |
chr4 | 26579084 | 26761223 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2967 | 151 | 45 | 23 | 67 | 5 | 10 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0001t0002 | 0/0 | 2967 | 4 | 0 | 1 | 1 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0001t0003 | 0/0 | 2967 | 8 | 7 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0001t0004 | 0/0 | 2967 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0001t0007 | 0/0 | 2967 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0001t0008 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0001t0009 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0002t0002 | 0/0 | 2967 | 103 | 19 | 16 | 50 | 6 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0002t0010 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0003t0001 | 0/0 | 2967 | 8 | 1 | 0 | 5 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0004t0001 | 1/0 | 2967 | 7 | 6 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0005t0001 | 0/0 | 2967 | 7 | 1 | 2 | 1 | 1 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0006t0001 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0006t0005 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0001c0010t0001 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0002c0007t0001 | 0/0 | 2967 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0003c0008t0006 | 0/0 | 2967 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| a0004c0009t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | AGTGT others(2962): Show |
chr4 | 26579084 | 26761223 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0010t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0003c0008t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0003c0008t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0004c0009t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0257 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0226 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0256 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0286 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00733 | hp2 | a0001 | c0005 | t0001 | g0104 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01069 | hp1 | a0001 | c0005 | t0001 | g0105 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0282 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01243 | hp1 | a0002 | c0007 | t0001 | g0166 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0272 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0222 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01517 | hp1 | a0001 | c0005 | t0001 | g0103 | EUR | IBS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0258 | EUR | IBS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0139 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0102 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0224 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0307 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02257 | hp1 | a0002 | c0007 | t0001 | g0163 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0306 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0175 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0274 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02615 | hp1 | a0002 | c0007 | t0001 | g0164 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02615 | hp2 | a0001 | c0010 | t0001 | g0034 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02622 | hp1 | a0001 | c0006 | t0005 | g0147 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0308 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0242 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0267 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0278 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0288 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0190 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0228 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02738 | hp2 | a0001 | c0005 | t0001 | g0106 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02970 | hp1 | a0002 | c0007 | t0001 | g0165 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03017 | hp1 | a0003 | c0008 | t0006 | g0114 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0142 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0290 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0211 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0273 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03491 | hp2 | a0003 | c0008 | t0006 | g0115 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0285 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0223 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0227 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0292 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0283 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0024 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0099 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0140 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18522 | hp2 | a0001 | c0006 | t0005 | g0207 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | CHB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0144 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0305 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18971 | hp1 | a0001 | c0002 | t0010 | g0266 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19083 | hp1 | a0004 | c0009 | t0001 | g0108 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19086 | hp1 | a0001 | c0005 | t0001 | g0092 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0215 | EUR | TSI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0309 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02486 | hp2 | a0001 | c0006 | t0005 | g0210 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0299 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0089 | REF | REF | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0138 | REF | REF | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26666355 | G | T | 1 | a0004 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.614G>T | p.Gly205Val | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/21 | 724/2967 | 614/1581 | 205/526 | chr4 | 26666355 | |||
| chr4:26673793 | A | G | 1 | a0002 | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.721A>G | p.Ser241Gly | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/21 | 831/2967 | 721/1581 | 241/526 | chr4 | 26673793 | |||
| chr4:26683735 | A | G | 1 | a0003 | 2 | HG03017.hp1 HG03491.hp2 |
missense_variant | MODERATE | c.877A>G | p.Ser293Gly | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/21 | 987/2967 | 877/1581 | 293/526 | chr4 | 26683735 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26584259 | C | T | 1 | a0001c0002 | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
synonymous_variant | LOW | c.66C>T | p.Ser22Ser | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/21 | 176/2967 | 66/1581 | 22/526 | chr4 | 26584259 | |||
| chr4:26659632 | C | T | 1 | a0001c0010 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.516C>T | p.Asn172Asn | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/21 | 626/2967 | 516/1581 | 172/526 | chr4 | 26659632 | |||
| chr4:26672165 | A | G | 9 | a0001c0001 a0001c0002 a0001c0003 others(6): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
synonymous_variant | LOW | c.681A>G | p.Glu227Glu | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/21 | 791/2967 | 681/1581 | 227/526 | chr4 | 26672165 | |||
| chr4:26717947 | T | C | 1 | a0001c0005 | 7 | HG00733.hp2 HG01069.hp1 HG01517.hp1 others(4): Show |
synonymous_variant | LOW | c.969T>C | p.Phe323Phe | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/21 | 1079/2967 | 969/1581 | 323/526 | chr4 | 26717947 | |||
| chr4:26718004 | A | G | 1 | a0001c0003 | 8 | HG01891.hp1 HG04184.hp2 HG04204.hp1 others(5): Show |
synonymous_variant | LOW | c.1026A>G | p.Lys342Lys | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/21 | 1136/2967 | 1026/1581 | 342/526 | chr4 | 26718004 | |||
| chr4:26748483 | A | G | 1 | a0001c0006 | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1392A>G | p.Leu464Leu | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/21 | 1502/2967 | 1392/1581 | 464/526 | chr4 | 26748483 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26584185 | G | A | 2 | a0001c0001t0003 a0003c0008t0006 |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-9G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/21 | 9 | chr4 | 26584185 | ||||||
| chr4:26755208 | T | G | 1 | a0001c0001t0004 | 4 | NA18979.hp2 NA18990.hp2 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*261T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 261 | chr4 | 26755208 | ||||||
| chr4:26755218 | A | G | 1 | a0001c0001t0008 | 2 | HG02922.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*271A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 271 | chr4 | 26755218 | ||||||
| chr4:26755233 | C | A | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0002t0002 others(2): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 286 | chr4 | 26755233 | ||||||
| chr4:26755540 | A | G | 1 | a0001c0001t0008 | 2 | HG02922.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*593A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 593 | chr4 | 26755540 | ||||||
| chr4:26755560 | A | T | 1 | a0001c0006t0005 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*613A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 613 | chr4 | 26755560 | ||||||
| chr4:26755565 | C | T | 1 | a0001c0002t0010 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 618 | chr4 | 26755565 | ||||||
| chr4:26755705 | A | G | 1 | a0001c0001t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 758 | chr4 | 26755705 | ||||||
| chr4:26755914 | C | T | 1 | a0001c0001t0007 | 2 | HG02083.hp1 NA18945.hp2 |
3_prime_UTR_variant | MODIFIER | c.*967C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 967 | chr4 | 26755914 | ||||||
| chr4:26755925 | C | T | 1 | a0001c0001t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*978C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 978 | chr4 | 26755925 | ||||||
| chr4:26756082 | G | A | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0010 |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 1135 | chr4 | 26756082 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26584329 | G | C | 1 | a0001c0001t0001g0002 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.99+37G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26584329 | |||||||
| chr4:26584349 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.99+57T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26584349 | |||||||
| chr4:26584424 | G | GACAAAA | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 |
3 | HG00639.hp2 HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.99+163_99+168dupAC others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584424 | ||||||
| chr4:26584424 | GACAAAA | G | 104 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(101): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.99+163_99+168delAC others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584424 | ||||||
| chr4:26584424 | GACAAAAA others(5): Show |
G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+157_99+168delAC others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584424 | ||||||
| chr4:26584432 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99+140C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26584432 | |||||||
| chr4:26584450 | CA | C | 3 | a0001c0001t0001g0002 a0001c0002t0002g0303 a0001c0002t0002g0304 |
3 | NA18963.hp1 NA19089.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.99+163delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584450 | ||||||
| chr4:26585086 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+794G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585086 | |||||||
| chr4:26585208 | G | C | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 |
3 | HG03490.hp2 HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.99+916G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585208 | |||||||
| chr4:26585210 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.99+918G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585210 | |||||||
| chr4:26585228 | C | T | 3 | a0001c0002t0002g0300 a0001c0002t0002g0301 a0001c0002t0002g0302 |
3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.99+936C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585228 | |||||||
| chr4:26585278 | A | G | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+986A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585278 | |||||||
| chr4:26585319 | T | C | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.99+1027T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585319 | |||||||
| chr4:26585435 | A | G | 2 | a0001c0001t0001g0191 a0001c0005t0001g0190 |
2 | HG02145.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.99+1143A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585435 | |||||||
| chr4:26585476 | TA | T | 19 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+1194delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26585476 | ||||||
| chr4:26585488 | A | T | 15 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(12): Show |
15 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+1196A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585488 | |||||||
| chr4:26585653 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.99+1361G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585653 | |||||||
| chr4:26585690 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99+1398C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585690 | |||||||
| chr4:26585696 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.99+1404G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585696 | |||||||
| chr4:26585821 | G | T | 1 | a0001c0002t0002g0299 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+1529G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585821 | |||||||
| chr4:26585919 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99+1627G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585919 | |||||||
| chr4:26586115 | GTGTGATC others(5): Show |
G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+1836_99+1847del others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586115 | ||||||
| chr4:26586170 | GC | G | 103 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0002t0002g0001 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.99+1879delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586170 | |||||||
| chr4:26586171 | C | CT | 18 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0100 others(15): Show |
18 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+1897dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586171 | ||||||
| chr4:26586171 | C | T | 3 | a0001c0001t0002g0116 a0001c0002t0002g0212 a0001c0002t0002g0213 |
3 | HG02622.hp2 HG04204.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.99+1879C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586171 | |||||||
| chr4:26586171 | CT | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0110 others(45): Show |
48 | HG00609.hp1 HG00733.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.99+1897delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586171 | ||||||
| chr4:26586558 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2266G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586558 | |||||||
| chr4:26586561 | AT | A | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+2274delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586561 | ||||||
| chr4:26586885 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0112 |
2 | NA18944.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.99+2593A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586885 | |||||||
| chr4:26587056 | A | G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2764A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587056 | |||||||
| chr4:26587251 | T | G | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+2959T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587251 | |||||||
| chr4:26587358 | G | A | 1 | a0001c0002t0002g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+3066G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587358 | |||||||
| chr4:26587403 | C | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+3111C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587403 | |||||||
| chr4:26587448 | G | A | 69 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0002t0002g0001 others(66): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+3156G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587448 | |||||||
| chr4:26587576 | CA | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.99+3301delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26587576 | ||||||
| chr4:26587576 | CAA | C | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0167 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+3300_99+3301del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26587576 | ||||||
| chr4:26587897 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.99+3605G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587897 | |||||||
| chr4:26588000 | C | T | 1 | a0001c0004t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+3708C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588000 | |||||||
| chr4:26588024 | C | CT | 39 | a0001c0001t0001g0009 a0001c0001t0001g0109 a0001c0001t0001g0143 others(36): Show |
39 | HG00733.hp1 HG00741.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+3751dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26588024 | ||||||
| chr4:26588087 | A | G | 4 | a0001c0002t0002g0213 a0001c0002t0002g0295 a0001c0002t0002g0296 others(1): Show |
4 | NA18944.hp2 NA18971.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3795A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588087 | |||||||
| chr4:26588111 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.99+3819C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588111 | |||||||
| chr4:26588121 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.99+3829G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588121 | |||||||
| chr4:26588138 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.99+3846A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588138 | |||||||
| chr4:26588183 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+3891G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588183 | |||||||
| chr4:26588226 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+3934C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588226 | |||||||
| chr4:26588272 | G | A | 3 | a0001c0002t0002g0215 a0003c0008t0006g0114 a0003c0008t0006g0115 |
3 | HG03017.hp1 HG03491.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.99+3980G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588272 | |||||||
| chr4:26588416 | GT | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.99+4128delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26588416 | ||||||
| chr4:26588870 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.99+4578A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588870 | |||||||
| chr4:26588884 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.99+4592G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588884 | |||||||
| chr4:26588976 | T | C | 7 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(4): Show |
7 | HG00741.hp2 HG01167.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+4684T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588976 | |||||||
| chr4:26589033 | A | G | 1 | a0001c0002t0002g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.99+4741A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589033 | |||||||
| chr4:26589085 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99+4793G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589085 | |||||||
| chr4:26589167 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.99+4875C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589167 | |||||||
| chr4:26589199 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(22): Show |
25 | HG00609.hp1 HG02257.hp2 NA18957.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+4907C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589199 | |||||||
| chr4:26589262 | G | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4970G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589262 | |||||||
| chr4:26589283 | AAAC | A | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+5012_99+5014del others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26589283 | ||||||
| chr4:26589364 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+5072A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589364 | |||||||
| chr4:26589564 | C | T | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.99+5272C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589564 | |||||||
| chr4:26589631 | A | G | 107 | a0001c0001t0001g0113 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.99+5339A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589631 | |||||||
| chr4:26589744 | T | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+5452T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589744 | |||||||
| chr4:26589757 | C | A | 69 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0002t0002g0001 others(66): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+5465C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589757 | |||||||
| chr4:26589822 | T | G | 3 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0299 |
3 | HG01981.hp2 HG02559.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.99+5530T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589822 | |||||||
| chr4:26590429 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.99+6137G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590429 | |||||||
| chr4:26590529 | T | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+6237T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590529 | |||||||
| chr4:26590796 | G | GT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+6535dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTT | 13 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
13 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+6534_99+6535dup others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTT | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(16): Show |
19 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+6530_99+6535dup others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0039 others(18): Show |
21 | HG00140.hp1 HG01257.hp1 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+6529_99+6535dup others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(1): Show |
28 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+6528_99+6535dup others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(2): Show |
23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(20): Show |
23 | HG00323.hp1 HG00544.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+6527_99+6535dup others(9): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(3): Show |
9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
9 | HG00621.hp2 HG02080.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+6526_99+6535dup others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0109 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.99+6525_99+6535dup others(11): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0001g0101 a0001c0005t0001g0102 a0001c0005t0001g0103 |
3 | HG01517.hp1 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.99+6524_99+6535dup others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0001g0155 a0001c0005t0001g0104 a0001c0005t0001g0105 |
3 | HG00733.hp2 HG01069.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.99+6523_99+6535dup others(13): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | G | GTTTTTTT others(7): Show |
1 | a0001c0005t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+6522_99+6535dup others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | GT | G | 100 | a0001c0001t0001g0113 a0001c0001t0001g0157 a0001c0001t0001g0158 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.99+6535delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | GTT | G | 12 | a0001c0001t0001g0156 a0001c0001t0003g0192 a0001c0001t0003g0193 others(9): Show |
12 | HG00741.hp1 HG01109.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6534_99+6535del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590796 | GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.99+6518_99+6535del others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | ||||||
| chr4:26590809 | T | G | 5 | a0001c0001t0002g0116 a0001c0002t0002g0001 a0001c0002t0002g0267 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+6517T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590809 | |||||||
| chr4:26590810 | T | G | 96 | a0001c0001t0001g0113 a0001c0001t0002g0152 a0001c0001t0002g0153 others(93): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.99+6518T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590810 | |||||||
| chr4:26590811 | T | G | 11 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(8): Show |
11 | HG01109.hp2 HG01256.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+6519T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590811 | |||||||
| chr4:26590838 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+6546G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590838 | |||||||
| chr4:26591074 | CT | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.99+6783delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591074 | |||||||
| chr4:26591261 | G | A | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+6969G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591261 | |||||||
| chr4:26591310 | T | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7018T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591310 | |||||||
| chr4:26591528 | A | C | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.99+7236A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591528 | |||||||
| chr4:26591587 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+7295C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591587 | |||||||
| chr4:26591682 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+7390A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591682 | |||||||
| chr4:26591701 | T | C | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+7409T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591701 | |||||||
| chr4:26591716 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+7424G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591716 | |||||||
| chr4:26591891 | C | G | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99+7599C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591891 | |||||||
| chr4:26591948 | A | G | 1 | a0001c0002t0002g0213 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.99+7656A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591948 | |||||||
| chr4:26591994 | C | T | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+7702C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591994 | |||||||
| chr4:26592034 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+7742A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592034 | |||||||
| chr4:26592061 | C | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+7769C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592061 | |||||||
| chr4:26592262 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+7970A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592262 | |||||||
| chr4:26592361 | G | A | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+8069G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592361 | |||||||
| chr4:26592452 | A | G | 106 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.99+8160A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592452 | |||||||
| chr4:26592463 | A | G | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+8171A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592463 | |||||||
| chr4:26592501 | G | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+8209G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592501 | |||||||
| chr4:26592522 | CA | C | 23 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(20): Show |
23 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+8232delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26592522 | ||||||
| chr4:26592899 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.99+8607A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592899 | |||||||
| chr4:26592984 | G | A | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+8692G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592984 | |||||||
| chr4:26593060 | A | G | 3 | a0001c0002t0002g0272 a0001c0002t0002g0292 a0001c0002t0002g0294 |
3 | HG01256.hp2 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.99+8768A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593060 | |||||||
| chr4:26593064 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+8772C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593064 | |||||||
| chr4:26593075 | G | C | 116 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(113): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+8783G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593075 | |||||||
| chr4:26593098 | G | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+8806G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593098 | |||||||
| chr4:26593402 | G | C | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+9110G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593402 | |||||||
| chr4:26593454 | A | G | 1 | a0001c0003t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.99+9162A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593454 | |||||||
| chr4:26593477 | A | G | 106 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.99+9185A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593477 | |||||||
| chr4:26593536 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.99+9244G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593536 | |||||||
| chr4:26593665 | A | G | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+9373A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593665 | |||||||
| chr4:26593817 | G | A | 1 | a0001c0002t0002g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+9525G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593817 | |||||||
| chr4:26593957 | A | G | 1 | a0001c0002t0002g0291 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.99+9665A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593957 | |||||||
| chr4:26594053 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.99+9761C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594053 | |||||||
| chr4:26594084 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+9792C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594084 | |||||||
| chr4:26594160 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+9868A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594160 | |||||||
| chr4:26594234 | G | A | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+9942G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594234 | |||||||
| chr4:26594251 | A | G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+9959A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594251 | |||||||
| chr4:26594371 | A | G | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+10079A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594371 | |||||||
| chr4:26594375 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10083G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594375 | |||||||
| chr4:26594396 | C | T | 9 | a0001c0002t0002g0203 a0001c0002t0002g0225 a0001c0002t0002g0262 others(6): Show |
9 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+10104C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594396 | |||||||
| chr4:26594564 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.99+10272C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594564 | |||||||
| chr4:26594907 | T | C | 1 | a0001c0002t0002g0226 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.99+10615T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594907 | |||||||
| chr4:26595061 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+10769A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595061 | |||||||
| chr4:26595071 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+10779G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595071 | |||||||
| chr4:26595078 | T | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+10786T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595078 | |||||||
| chr4:26595282 | G | A | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | NA18957.hp1 NA18964.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+10990G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595282 | |||||||
| chr4:26595546 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+11254A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595546 | |||||||
| chr4:26595554 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.99+11262C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595554 | |||||||
| chr4:26595605 | G | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.99+11313G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595605 | |||||||
| chr4:26595664 | C | T | 1 | a0001c0002t0002g0299 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+11372C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595664 | |||||||
| chr4:26595743 | C | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+11451C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595743 | |||||||
| chr4:26595853 | G | A | 22 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(19): Show |
22 | HG00733.hp1 HG01243.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.99+11561G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595853 | |||||||
| chr4:26595966 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.99+11674A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595966 | |||||||
| chr4:26596031 | T | A | 116 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(113): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+11739T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596031 | |||||||
| chr4:26596048 | C | G | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11756C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596048 | |||||||
| chr4:26596080 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.99+11788T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596080 | |||||||
| chr4:26596104 | G | A | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11812G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596104 | |||||||
| chr4:26596176 | C | T | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11884C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596176 | |||||||
| chr4:26596222 | G | A | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11930G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596222 | |||||||
| chr4:26596436 | A | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+12144A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596436 | |||||||
| chr4:26596455 | C | CGT | 16 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0001g0129 others(13): Show |
16 | HG00544.hp1 HG01109.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+12195_99+12196d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | ||||||
| chr4:26596455 | C | CGTGT | 34 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(31): Show |
34 | HG00733.hp1 HG02258.hp1 HG02451.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+12193_99+12196d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | ||||||
| chr4:26596455 | CGT | C | 72 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0093 others(69): Show |
73 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.99+12195_99+12196d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | ||||||
| chr4:26596455 | CGTGT | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0054 others(6): Show |
9 | HG02257.hp2 HG03927.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+12193_99+12196d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | ||||||
| chr4:26596455 | CGTGTGTG others(7): Show |
C | 15 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(12): Show |
15 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+12183_99+12196d others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | ||||||
| chr4:26596487 | T | A | 11 | a0001c0001t0001g0005 a0001c0001t0003g0192 a0001c0001t0003g0193 others(8): Show |
11 | HG00639.hp2 HG01109.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+12195T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596487 | |||||||
| chr4:26596511 | T | C | 1 | a0001c0004t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+12219T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596511 | |||||||
| chr4:26596617 | G | GT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.99+12339dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596617 | ||||||
| chr4:26596760 | C | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+12468C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596760 | |||||||
| chr4:26596771 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.99+12479C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596771 | |||||||
| chr4:26596905 | G | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.99+12613G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596905 | |||||||
| chr4:26596957 | A | C | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.99+12665A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596957 | |||||||
| chr4:26597229 | A | C | 1 | a0001c0005t0001g0103 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.99+12937A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597229 | |||||||
| chr4:26597231 | G | T | 1 | a0001c0005t0001g0103 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.99+12939G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597231 | |||||||
| chr4:26597523 | C | CT | 23 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0072 others(20): Show |
23 | HG00621.hp1 HG01109.hp2 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+13251dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26597523 | ||||||
| chr4:26597529 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.99+13237T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597529 | |||||||
| chr4:26597543 | TA | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0156 a0001c0001t0001g0157 others(12): Show |
15 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+13253delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26597543 | ||||||
| chr4:26597544 | A | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.99+13252A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597544 | |||||||
| chr4:26597625 | A | G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+13333A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597625 | |||||||
| chr4:26597634 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+13342G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597634 | |||||||
| chr4:26597650 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+13358C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597650 | |||||||
| chr4:26597951 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.99+13659T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597951 | |||||||
| chr4:26598183 | T | C | 1 | a0001c0001t0004g0023 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99+13891T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598183 | |||||||
| chr4:26598399 | CT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+14117delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26598399 | ||||||
| chr4:26598570 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+14278A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598570 | |||||||
| chr4:26598711 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.99+14419A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598711 | |||||||
| chr4:26598831 | A | G | 112 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0097 others(109): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.100-14338A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598831 | |||||||
| chr4:26598918 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-14251T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598918 | |||||||
| chr4:26598947 | AAATAGAA others(11): Show |
A | 19 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-14212_100-1419 others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26598947 | ||||||
| chr4:26598993 | T | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.100-14176T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598993 | |||||||
| chr4:26599025 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-14144A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599025 | |||||||
| chr4:26599070 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-14099G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599070 | |||||||
| chr4:26599130 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.100-14039T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599130 | |||||||
| chr4:26599583 | G | T | 1 | a0001c0004t0001g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-13586G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599583 | |||||||
| chr4:26599611 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.100-13558C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599611 | |||||||
| chr4:26599683 | C | T | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-13486C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599683 | |||||||
| chr4:26599751 | G | T | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13418G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599751 | |||||||
| chr4:26599939 | C | G | 23 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(20): Show |
23 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-13230C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599939 | |||||||
| chr4:26599950 | C | CA | 6 | a0001c0001t0001g0117 a0001c0001t0001g0149 a0001c0001t0001g0191 others(3): Show |
6 | HG02145.hp2 HG03471.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-13194dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26599950 | ||||||
| chr4:26599950 | CA | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.100-13194delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26599950 | ||||||
| chr4:26599951 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-13218A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599951 | |||||||
| chr4:26599977 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-13192A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599977 | |||||||
| chr4:26600341 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.100-12828T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600341 | |||||||
| chr4:26600387 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-12782C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600387 | |||||||
| chr4:26600543 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-12626T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600543 | |||||||
| chr4:26600619 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100-12550G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600619 | |||||||
| chr4:26600678 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.100-12491G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600678 | |||||||
| chr4:26600685 | T | C | 1 | a0001c0002t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.100-12484T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600685 | |||||||
| chr4:26600954 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.100-12215T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600954 | |||||||
| chr4:26600990 | T | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA18965.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.100-12179T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600990 | |||||||
| chr4:26601131 | CTA | C | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.100-12025_100-1202 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26601131 | ||||||
| chr4:26601229 | C | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-11940C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601229 | |||||||
| chr4:26601344 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.100-11825G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601344 | |||||||
| chr4:26601484 | G | A | 3 | a0001c0002t0002g0282 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.100-11685G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601484 | |||||||
| chr4:26601666 | G | T | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.100-11503G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601666 | |||||||
| chr4:26601839 | A | G | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.100-11330A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601839 | |||||||
| chr4:26602150 | C | G | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-11019C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602150 | |||||||
| chr4:26602342 | A | G | 4 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 others(1): Show |
4 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-10827A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602342 | |||||||
| chr4:26602401 | A | G | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-10768A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602401 | |||||||
| chr4:26602435 | C | CT | 13 | a0001c0001t0001g0137 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
13 | HG00621.hp1 HG00733.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-10710dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | ||||||
| chr4:26602435 | CT | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.100-10710delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | ||||||
| chr4:26602435 | CTT | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0039 others(11): Show |
14 | HG00609.hp2 HG01109.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-10711_100-1071 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | ||||||
| chr4:26602435 | CTTT | C | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG02886.hp1 HG02976.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-10712_100-1071 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | ||||||
| chr4:26602487 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.100-10682G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602487 | |||||||
| chr4:26602536 | G | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.100-10633G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602536 | |||||||
| chr4:26602849 | T | G | 1 | a0001c0002t0002g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-10320T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602849 | |||||||
| chr4:26603220 | T | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9949T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603220 | |||||||
| chr4:26603285 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100-9884T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603285 | |||||||
| chr4:26603321 | T | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.100-9848T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603321 | |||||||
| chr4:26603353 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.100-9816A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603353 | |||||||
| chr4:26603359 | T | G | 1 | a0001c0002t0002g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-9810T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603359 | |||||||
| chr4:26603452 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-9717A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603452 | |||||||
| chr4:26603562 | G | A | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-9607G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603562 | |||||||
| chr4:26603661 | C | T | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-9508C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603661 | |||||||
| chr4:26603687 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.100-9482A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603687 | |||||||
| chr4:26603981 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.100-9188C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603981 | |||||||
| chr4:26604006 | C | G | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100-9163C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604006 | |||||||
| chr4:26604130 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.100-9039T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604130 | |||||||
| chr4:26604148 | C | CT | 17 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0149 others(14): Show |
17 | HG00609.hp1 HG01109.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-8998dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604148 | ||||||
| chr4:26604148 | CT | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0156 a0001c0001t0001g0157 others(19): Show |
22 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-8998delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604148 | ||||||
| chr4:26604148 | CTTTTTTT | C | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-9004_100-8998d others(9): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604148 | ||||||
| chr4:26604153 | T | TC | 3 | a0001c0001t0001g0035 a0001c0005t0001g0103 a0001c0005t0001g0104 |
3 | HG00733.hp2 HG01517.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.100-9016_100-9015i others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604153 | |||||||
| chr4:26604154 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.100-9015T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604154 | |||||||
| chr4:26604155 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0169 |
2 | HG01167.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-9014T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604155 | |||||||
| chr4:26604160 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100-9009T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604160 | |||||||
| chr4:26604233 | C | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.100-8936C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604233 | |||||||
| chr4:26604310 | G | A | 1 | a0001c0002t0002g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-8859G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604310 | |||||||
| chr4:26604314 | G | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-8855G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604314 | |||||||
| chr4:26604411 | C | T | 21 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(18): Show |
21 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-8758C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604411 | |||||||
| chr4:26604539 | A | G | 1 | a0002c0007t0001g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.100-8630A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604539 | |||||||
| chr4:26604549 | A | T | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.100-8620A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604549 | |||||||
| chr4:26604804 | C | G | 36 | a0001c0001t0002g0019 a0001c0002t0002g0001 a0001c0002t0002g0200 others(33): Show |
37 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.100-8365C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604804 | |||||||
| chr4:26604831 | A | G | 1 | a0001c0002t0002g0242 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-8338A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604831 | |||||||
| chr4:26604884 | AAAT | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.100-8264_100-8262d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604884 | ||||||
| chr4:26604884 | AAATAAT | A | 40 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.100-8267_100-8262d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604884 | ||||||
| chr4:26604930 | G | C | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-8239G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604930 | |||||||
| chr4:26604974 | T | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0028 |
2 | HG02165.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.100-8195T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604974 | |||||||
| chr4:26605046 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.100-8123A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605046 | |||||||
| chr4:26605160 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-8009G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605160 | |||||||
| chr4:26605210 | C | A | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-7959C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605210 | |||||||
| chr4:26605351 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-7818A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605351 | |||||||
| chr4:26605352 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-7817T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605352 | |||||||
| chr4:26605380 | G | A | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.100-7789G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605380 | |||||||
| chr4:26605535 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100-7634G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605535 | |||||||
| chr4:26605622 | T | C | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7547T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605622 | |||||||
| chr4:26605660 | A | C | 1 | a0001c0001t0001g0037 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100-7509A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605660 | |||||||
| chr4:26605701 | A | C | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-7468A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605701 | |||||||
| chr4:26605737 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100-7432A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605737 | |||||||
| chr4:26605739 | C | T | 1 | a0001c0002t0002g0297 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100-7430C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605739 | |||||||
| chr4:26605814 | G | A | 106 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.100-7355G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605814 | |||||||
| chr4:26605820 | T | A | 1 | a0001c0003t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.100-7349T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605820 | |||||||
| chr4:26605826 | T | C | 1 | a0001c0003t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.100-7343T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605826 | |||||||
| chr4:26605831 | T | C | 1 | a0001c0003t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.100-7338T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605831 | |||||||
| chr4:26605849 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.100-7320T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605849 | |||||||
| chr4:26605991 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.100-7178C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605991 | |||||||
| chr4:26606049 | G | T | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.100-7120G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606049 | |||||||
| chr4:26606127 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.100-7042G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606127 | |||||||
| chr4:26606326 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-6843A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606326 | |||||||
| chr4:26606335 | G | A | 1 | a0001c0002t0002g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.100-6834G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606335 | |||||||
| chr4:26606369 | T | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.100-6800T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606369 | |||||||
| chr4:26606589 | G | T | 1 | a0001c0002t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.100-6580G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606589 | |||||||
| chr4:26606724 | C | T | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-6445C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606724 | |||||||
| chr4:26606848 | TC | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-6319delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26606848 | ||||||
| chr4:26607247 | A | G | 19 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0171 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-5922A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607247 | |||||||
| chr4:26607353 | A | G | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100-5816A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607353 | |||||||
| chr4:26607357 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-5812T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607357 | |||||||
| chr4:26607544 | T | A | 1 | a0001c0002t0002g0287 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-5625T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607544 | |||||||
| chr4:26607557 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100-5612A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607557 | |||||||
| chr4:26607579 | A | G | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-5590A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607579 | |||||||
| chr4:26607620 | G | A | 2 | a0001c0001t0003g0193 a0001c0001t0003g0194 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.100-5549G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607620 | |||||||
| chr4:26607824 | A | G | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-5345A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607824 | |||||||
| chr4:26608009 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.100-5160G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608009 | |||||||
| chr4:26608263 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-4906A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608263 | |||||||
| chr4:26608655 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.100-4514C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608655 | |||||||
| chr4:26608945 | G | A | 92 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(89): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.100-4224G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608945 | |||||||
| chr4:26609046 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.100-4123T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609046 | |||||||
| chr4:26609060 | G | A | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.100-4109G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609060 | |||||||
| chr4:26609063 | A | AG | 30 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0069 others(27): Show |
30 | HG00741.hp1 HG01168.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.100-4100dupG | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26609063 | ||||||
| chr4:26609066 | G | A | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-4103G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609066 | |||||||
| chr4:26609070 | A | AG | 9 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0078 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-4093dupG | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26609070 | ||||||
| chr4:26609070 | A | G | 4 | a0001c0001t0001g0091 a0001c0002t0002g0224 a0001c0002t0002g0228 others(1): Show |
4 | HG01981.hp2 HG02135.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-4099A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609070 | |||||||
| chr4:26609221 | T | A | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-3948T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609221 | |||||||
| chr4:26609347 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.100-3822T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609347 | |||||||
| chr4:26609367 | T | G | 1 | a0001c0002t0002g0234 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.100-3802T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609367 | |||||||
| chr4:26609672 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100-3497G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609672 | |||||||
| chr4:26609828 | C | T | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100-3341C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609828 | |||||||
| chr4:26609912 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-3257G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609912 | |||||||
| chr4:26609926 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-3243A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609926 | |||||||
| chr4:26610278 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0051 |
2 | NA19054.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.100-2891G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610278 | |||||||
| chr4:26610414 | C | CT | 9 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0003g0196 others(6): Show |
9 | HG00323.hp2 HG00741.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2738dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26610414 | ||||||
| chr4:26610414 | CT | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0107 others(10): Show |
13 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-2738delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26610414 | ||||||
| chr4:26610436 | G | C | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.100-2733G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610436 | |||||||
| chr4:26610544 | C | T | 9 | a0001c0001t0003g0192 a0001c0001t0003g0195 a0001c0001t0003g0196 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2625C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610544 | |||||||
| chr4:26610617 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100-2552A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610617 | |||||||
| chr4:26610916 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.100-2253C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610916 | |||||||
| chr4:26611096 | C | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0082 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.100-2073C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611096 | |||||||
| chr4:26611306 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-1863C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611306 | |||||||
| chr4:26611460 | T | TATAAGGT others(9): Show |
1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1709_100-1708i others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611460 | |||||||
| chr4:26611461 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1708T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611461 | |||||||
| chr4:26611464 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-1705A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611464 | |||||||
| chr4:26611508 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-1661C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611508 | |||||||
| chr4:26611833 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.100-1336T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611833 | |||||||
| chr4:26612263 | T | A | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-906T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612263 | |||||||
| chr4:26612277 | G | T | 2 | a0001c0002t0002g0272 a0001c0002t0002g0294 |
2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.100-892G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612277 | |||||||
| chr4:26612278 | C | G | 2 | a0001c0002t0002g0272 a0001c0002t0002g0294 |
2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.100-891C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612278 | |||||||
| chr4:26612377 | G | T | 1 | a0001c0006t0005g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-792G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612377 | |||||||
| chr4:26612488 | C | G | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.100-681C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612488 | |||||||
| chr4:26612511 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.100-658G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612511 | |||||||
| chr4:26612670 | A | G | 1 | a0001c0002t0002g0278 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-499A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612670 | |||||||
| chr4:26612836 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.100-333A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612836 | |||||||
| chr4:26612850 | T | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-319T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612850 | |||||||
| chr4:26612941 | T | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.100-228T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612941 | |||||||
| chr4:26613146 | T | A | 1 | a0001c0010t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-23T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26613146 | |||||||
| chr4:26613345 | C | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+104C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613345 | |||||||
| chr4:26613549 | A | G | 3 | a0001c0006t0005g0147 a0001c0006t0005g0207 a0001c0006t0005g0210 |
3 | HG02486.hp2 HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.172+308A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613549 | |||||||
| chr4:26613579 | C | T | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.172+338C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613579 | |||||||
| chr4:26613815 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.172+574A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613815 | |||||||
| chr4:26613858 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.173-550G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613858 | |||||||
| chr4:26613885 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.173-523T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613885 | |||||||
| chr4:26614360 | C | T | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.173-48C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26614360 | |||||||
| chr4:26614382 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.173-26T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26614382 | |||||||
| chr4:26614549 | ATTAT | A | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.218+101_218+104del others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 26614549 | ||||||
| chr4:26614574 | G | A | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.218+121G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614574 | |||||||
| chr4:26614612 | G | A | 5 | a0001c0002t0002g0302 a0002c0007t0001g0163 a0002c0007t0001g0164 others(2): Show |
5 | HG01243.hp1 HG02155.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+159G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614612 | |||||||
| chr4:26614764 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.218+311G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614764 | |||||||
| chr4:26614788 | G | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+335G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614788 | |||||||
| chr4:26615353 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.218+900G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615353 | |||||||
| chr4:26615393 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218+940A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615393 | |||||||
| chr4:26615416 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+963C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615416 | |||||||
| chr4:26615449 | C | A | 1 | a0001c0001t0001g0045 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.218+996C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615449 | |||||||
| chr4:26615455 | C | CT | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.218+1015dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 26615455 | ||||||
| chr4:26615460 | T | A | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1007T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615460 | |||||||
| chr4:26615562 | A | G | 2 | a0001c0002t0002g0223 a0001c0002t0002g0224 |
2 | HG01981.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.218+1109A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615562 | |||||||
| chr4:26615698 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0004g0022 |
3 | NA18955.hp1 NA19009.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.218+1245T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615698 | |||||||
| chr4:26615803 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.218+1350C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615803 | |||||||
| chr4:26615816 | T | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.218+1363T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615816 | |||||||
| chr4:26615862 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.218+1409G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615862 | |||||||
| chr4:26616053 | G | T | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+1600G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616053 | |||||||
| chr4:26616072 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0185 others(1): Show |
4 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1619T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616072 | |||||||
| chr4:26616098 | T | C | 11 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+1645T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616098 | |||||||
| chr4:26616140 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+1687G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616140 | |||||||
| chr4:26616206 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218+1753A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616206 | |||||||
| chr4:26616342 | C | A | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.218+1889C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616342 | |||||||
| chr4:26616414 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+1961G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616414 | |||||||
| chr4:26616468 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+2015A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616468 | |||||||
| chr4:26616542 | A | G | 1 | a0001c0001t0008g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.218+2089A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616542 | |||||||
| chr4:26616709 | C | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+2256C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616709 | |||||||
| chr4:26616860 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+2407G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616860 | |||||||
| chr4:26617089 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.218+2636C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617089 | |||||||
| chr4:26617321 | A | T | 1 | a0001c0002t0002g0213 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.218+2868A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617321 | |||||||
| chr4:26617343 | A | G | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.218+2890A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617343 | |||||||
| chr4:26617463 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218+3010C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617463 | |||||||
| chr4:26617803 | A | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-2810A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617803 | |||||||
| chr4:26617914 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.219-2699C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617914 | |||||||
| chr4:26617975 | A | G | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.219-2638A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617975 | |||||||
| chr4:26618180 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219-2433G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618180 | |||||||
| chr4:26618209 | T | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.219-2404T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618209 | |||||||
| chr4:26618351 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219-2262G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618351 | |||||||
| chr4:26618535 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.219-2078G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618535 | |||||||
| chr4:26618653 | G | C | 2 | a0001c0001t0002g0116 a0001c0001t0002g0152 |
2 | HG00642.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.219-1960G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618653 | |||||||
| chr4:26618876 | T | C | 1 | a0001c0004t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.219-1737T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618876 | |||||||
| chr4:26618919 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219-1694T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618919 | |||||||
| chr4:26618932 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.219-1681C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618932 | |||||||
| chr4:26618978 | A | G | 18 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0171 others(15): Show |
18 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-1635A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618978 | |||||||
| chr4:26619119 | T | G | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-1494T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619119 | |||||||
| chr4:26619167 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219-1446A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619167 | |||||||
| chr4:26619227 | C | T | 105 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.219-1386C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619227 | |||||||
| chr4:26619379 | G | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219-1234G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619379 | |||||||
| chr4:26619425 | T | C | 1 | a0001c0002t0002g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.219-1188T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619425 | |||||||
| chr4:26619611 | A | T | 1 | a0003c0008t0006g0115 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.219-1002A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619611 | |||||||
| chr4:26619651 | T | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.219-962T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619651 | |||||||
| chr4:26619668 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.219-945C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619668 | |||||||
| chr4:26619804 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.219-809T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619804 | |||||||
| chr4:26619842 | G | A | 1 | a0001c0002t0002g0235 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-771G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619842 | |||||||
| chr4:26619850 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.219-763T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619850 | |||||||
| chr4:26619970 | C | T | 1 | a0001c0001t0008g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.219-643C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619970 | |||||||
| chr4:26620098 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.219-515T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620098 | |||||||
| chr4:26620167 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219-446C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620167 | |||||||
| chr4:26620194 | A | G | 1 | a0002c0007t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.219-419A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620194 | |||||||
| chr4:26620385 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.219-228G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620385 | |||||||
| chr4:26620388 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.219-225C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620388 | |||||||
| chr4:26620456 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.219-157T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620456 | |||||||
| chr4:26620607 | T | C | 4 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.219-6T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620607 | |||||||
| chr4:26620988 | C | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.294+300C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26620988 | |||||||
| chr4:26621002 | G | A | 1 | a0001c0002t0002g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.294+314G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621002 | |||||||
| chr4:26621610 | C | T | 3 | a0001c0002t0002g0241 a0001c0002t0002g0256 a0001c0004t0001g0142 |
3 | HG00280.hp2 HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.294+922C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621610 | |||||||
| chr4:26621616 | T | C | 1 | a0004c0009t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.294+928T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621616 | |||||||
| chr4:26621810 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.294+1122G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621810 | |||||||
| chr4:26621811 | T | G | 1 | a0001c0002t0002g0262 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.294+1123T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621811 | |||||||
| chr4:26621839 | A | C | 1 | a0001c0002t0002g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.294+1151A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621839 | |||||||
| chr4:26621848 | G | A | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+1160G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621848 | |||||||
| chr4:26621857 | C | T | 1 | a0001c0004t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.294+1169C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621857 | |||||||
| chr4:26621986 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.294+1298T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621986 | |||||||
| chr4:26622234 | TAAAGTA | T | 106 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.294+1547_294+1552d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622234 | |||||||
| chr4:26622387 | A | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0063 others(1): Show |
4 | HG01257.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1699A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622387 | |||||||
| chr4:26622422 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.294+1734T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622422 | |||||||
| chr4:26622589 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.294+1901A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622589 | |||||||
| chr4:26622657 | T | C | 4 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+1969T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622657 | |||||||
| chr4:26622994 | A | G | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+2306A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622994 | |||||||
| chr4:26623019 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+2331A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623019 | |||||||
| chr4:26623248 | C | G | 1 | a0001c0002t0002g0296 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.294+2560C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623248 | |||||||
| chr4:26623384 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.294+2696T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623384 | |||||||
| chr4:26623535 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.294+2847T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623535 | |||||||
| chr4:26623563 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.294+2875A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623563 | |||||||
| chr4:26624149 | C | T | 2 | a0001c0001t0001g0033 a0001c0010t0001g0034 |
2 | HG00642.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.294+3461C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624149 | |||||||
| chr4:26624191 | T | C | 1 | a0001c0003t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.294+3503T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624191 | |||||||
| chr4:26624372 | CT | C | 106 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.294+3693delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26624372 | ||||||
| chr4:26624420 | A | C | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294+3732A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624420 | |||||||
| chr4:26624490 | G | A | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+3802G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624490 | |||||||
| chr4:26624528 | A | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+3840A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624528 | |||||||
| chr4:26624774 | A | T | 1 | a0001c0002t0002g0291 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.294+4086A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624774 | |||||||
| chr4:26624781 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294+4093T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624781 | |||||||
| chr4:26624897 | C | T | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.294+4209C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624897 | |||||||
| chr4:26625018 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+4330C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625018 | |||||||
| chr4:26625135 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.294+4447G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625135 | |||||||
| chr4:26625145 | C | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+4457C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625145 | |||||||
| chr4:26625247 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.294+4559C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625247 | |||||||
| chr4:26625429 | C | T | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.294+4741C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625429 | |||||||
| chr4:26625506 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294+4818C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625506 | |||||||
| chr4:26625612 | T | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+4924T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625612 | |||||||
| chr4:26625924 | C | T | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.294+5236C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625924 | |||||||
| chr4:26626039 | T | G | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+5351T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626039 | |||||||
| chr4:26626494 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+5806G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626494 | |||||||
| chr4:26626609 | C | A | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.294+5921C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626609 | |||||||
| chr4:26626639 | A | G | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.294+5951A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626639 | |||||||
| chr4:26626818 | C | CT | 106 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.294+6138dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26626818 | ||||||
| chr4:26627038 | C | A | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+6350C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627038 | |||||||
| chr4:26627038 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.294+6350C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627038 | |||||||
| chr4:26627043 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+6355G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627043 | |||||||
| chr4:26627135 | C | T | 1 | a0001c0002t0002g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.294+6447C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627135 | |||||||
| chr4:26627412 | G | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.294+6724G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627412 | |||||||
| chr4:26627435 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.294+6747T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627435 | |||||||
| chr4:26627477 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.294+6789A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627477 | |||||||
| chr4:26627607 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+6919T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627607 | |||||||
| chr4:26627662 | G | T | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+6974G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627662 | |||||||
| chr4:26627709 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.294+7021T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627709 | |||||||
| chr4:26627874 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.294+7186G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627874 | |||||||
| chr4:26627950 | A | G | 1 | a0001c0004t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.294+7262A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627950 | |||||||
| chr4:26628015 | T | G | 1 | a0001c0005t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.294+7327T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628015 | |||||||
| chr4:26628204 | T | C | 1 | a0001c0002t0002g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.294+7516T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628204 | |||||||
| chr4:26628206 | G | A | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0125 others(3): Show |
6 | HG00609.hp1 NA18986.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+7518G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628206 | |||||||
| chr4:26628245 | G | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.294+7557G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628245 | |||||||
| chr4:26628299 | A | G | 1 | a0001c0005t0001g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.294+7611A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628299 | |||||||
| chr4:26628339 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294+7651C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628339 | |||||||
| chr4:26628399 | A | G | 1 | a0001c0002t0002g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.294+7711A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628399 | |||||||
| chr4:26628413 | G | A | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+7725G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628413 | |||||||
| chr4:26628719 | A | G | 1 | a0001c0001t0004g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.294+8031A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628719 | |||||||
| chr4:26628769 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0081 others(2): Show |
5 | HG00099.hp2 HG00323.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+8081A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628769 | |||||||
| chr4:26628791 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.294+8103C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628791 | |||||||
| chr4:26628912 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+8224A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628912 | |||||||
| chr4:26628915 | A | C | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+8227A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628915 | |||||||
| chr4:26629049 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.295-8162G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629049 | |||||||
| chr4:26629243 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.295-7968A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629243 | |||||||
| chr4:26629267 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.295-7944G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629267 | |||||||
| chr4:26629288 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.295-7923C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629288 | |||||||
| chr4:26629308 | A | T | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.295-7903A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629308 | |||||||
| chr4:26629438 | C | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.295-7773C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629438 | |||||||
| chr4:26629556 | A | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(26): Show |
29 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.295-7655A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629556 | |||||||
| chr4:26629646 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.295-7565A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629646 | |||||||
| chr4:26630187 | T | G | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-7024T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630187 | |||||||
| chr4:26630550 | T | C | 11 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-6661T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630550 | |||||||
| chr4:26630646 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.295-6565C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630646 | |||||||
| chr4:26630687 | T | G | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.295-6524T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630687 | |||||||
| chr4:26630720 | T | C | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.295-6491T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630720 | |||||||
| chr4:26630929 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.295-6282G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630929 | |||||||
| chr4:26631362 | C | T | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.295-5849C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631362 | |||||||
| chr4:26631479 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-5732T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631479 | |||||||
| chr4:26631521 | T | C | 3 | a0001c0002t0002g0234 a0001c0002t0002g0236 a0001c0002t0002g0250 |
3 | NA18957.hp2 NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.295-5690T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631521 | |||||||
| chr4:26631595 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.295-5616A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631595 | |||||||
| chr4:26631612 | C | T | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.295-5599C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631612 | |||||||
| chr4:26631673 | G | A | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-5538G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631673 | |||||||
| chr4:26632044 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-5167A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632044 | |||||||
| chr4:26632280 | C | T | 32 | a0001c0001t0002g0019 a0001c0002t0002g0001 a0001c0002t0002g0216 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-4931C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632280 | |||||||
| chr4:26632293 | C | T | 1 | a0001c0002t0002g0154 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.295-4918C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632293 | |||||||
| chr4:26632460 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.295-4751T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632460 | |||||||
| chr4:26632926 | G | T | 2 | a0001c0002t0002g0293 a0001c0002t0002g0304 |
2 | NA18963.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.295-4285G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632926 | |||||||
| chr4:26632997 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.295-4214C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632997 | |||||||
| chr4:26633031 | A | G | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-4180A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633031 | |||||||
| chr4:26633033 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.295-4178C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633033 | |||||||
| chr4:26633125 | T | C | 1 | a0001c0004t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295-4086T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633125 | |||||||
| chr4:26633132 | C | T | 118 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(115): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.295-4079C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633132 | |||||||
| chr4:26633177 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.295-4034A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633177 | |||||||
| chr4:26633226 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.295-3985C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633226 | |||||||
| chr4:26633492 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.295-3719G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633492 | |||||||
| chr4:26633763 | A | T | 1 | a0001c0001t0002g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.295-3448A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633763 | |||||||
| chr4:26633801 | C | T | 1 | a0001c0003t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.295-3410C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633801 | |||||||
| chr4:26633970 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(13): Show |
16 | HG01993.hp2 HG02015.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.295-3241C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633970 | |||||||
| chr4:26634048 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.295-3163A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634048 | |||||||
| chr4:26634060 | T | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-3151T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634060 | |||||||
| chr4:26634075 | C | CA | 25 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0046 others(22): Show |
25 | HG00544.hp2 HG00733.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.295-3122dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26634075 | ||||||
| chr4:26634075 | CA | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0001g0146 others(9): Show |
12 | HG01109.hp1 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-3122delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26634075 | ||||||
| chr4:26634198 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.295-3013A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634198 | |||||||
| chr4:26634214 | A | G | 2 | a0001c0002t0002g0238 a0001c0002t0002g0239 |
2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.295-2997A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634214 | |||||||
| chr4:26634283 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.295-2928G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634283 | |||||||
| chr4:26634706 | G | C | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.295-2505G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634706 | |||||||
| chr4:26634948 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.295-2263C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634948 | |||||||
| chr4:26635017 | A | G | 1 | a0001c0004t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295-2194A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635017 | |||||||
| chr4:26635036 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.295-2175G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635036 | |||||||
| chr4:26635113 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.295-2098A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635113 | |||||||
| chr4:26635327 | A | T | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.295-1884A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635327 | |||||||
| chr4:26635628 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0096 |
2 | HG00621.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.295-1583A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635628 | |||||||
| chr4:26635632 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.295-1579A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635632 | |||||||
| chr4:26635641 | A | T | 1 | a0001c0002t0002g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.295-1570A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635641 | |||||||
| chr4:26635766 | A | G | 14 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.295-1445A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635766 | |||||||
| chr4:26635832 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.295-1379A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635832 | |||||||
| chr4:26636015 | T | G | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.295-1196T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636015 | |||||||
| chr4:26636073 | A | T | 13 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(10): Show |
13 | HG00741.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-1138A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636073 | |||||||
| chr4:26636199 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.295-1012T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636199 | |||||||
| chr4:26636318 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.295-893T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636318 | |||||||
| chr4:26636439 | C | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(32): Show |
35 | HG00609.hp1 HG02145.hp2 HG02258.hp2 others(32): Show |
intron_variant | MODIFIER | c.295-772C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636439 | |||||||
| chr4:26636455 | A | G | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.295-756A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636455 | |||||||
| chr4:26636488 | T | TA | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(158): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.295-706dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26636488 | ||||||
| chr4:26636488 | T | TAA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.295-707_295-706dup others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26636488 | ||||||
| chr4:26636488 | T | TAG | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-722_295-721ins others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26636488 | ||||||
| chr4:26636611 | A | G | 1 | a0001c0003t0001g0024 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.295-600A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636611 | |||||||
| chr4:26636621 | T | A | 1 | a0001c0002t0002g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.295-590T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636621 | |||||||
| chr4:26636734 | C | G | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-477C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636734 | |||||||
| chr4:26636775 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.295-436T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636775 | |||||||
| chr4:26636828 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.295-383A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636828 | |||||||
| chr4:26636828 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.295-383A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636828 | |||||||
| chr4:26636844 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.295-367C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636844 | |||||||
| chr4:26636960 | C | G | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-251C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636960 | |||||||
| chr4:26637112 | C | T | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.295-99C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26637112 | |||||||
| chr4:26637436 | G | A | 1 | a0001c0002t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.369+151G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637436 | |||||||
| chr4:26637604 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.369+319C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637604 | |||||||
| chr4:26637619 | A | G | 12 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0001g0096 others(9): Show |
12 | HG00621.hp2 HG00733.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+334A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637619 | |||||||
| chr4:26637873 | T | C | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.369+588T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637873 | |||||||
| chr4:26637972 | G | A | 1 | a0001c0002t0002g0296 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.369+687G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637972 | |||||||
| chr4:26638005 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+720G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638005 | |||||||
| chr4:26638081 | AACATTTA others(346): Show |
A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-689_370-337del | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638081 | |||||||
| chr4:26638146 | A | T | 1 | a0001c0002t0002g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.370-625A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638146 | |||||||
| chr4:26638348 | A | C | 1 | a0004c0009t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.370-423A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638348 | |||||||
| chr4:26638674 | T | C | 1 | a0001c0005t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.370-97T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638674 | |||||||
| chr4:26638907 | A | G | 1 | a0001c0003t0001g0026 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.433+73A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26638907 | |||||||
| chr4:26639153 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.433+319G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639153 | |||||||
| chr4:26639362 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.433+528A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639362 | |||||||
| chr4:26639434 | TTCTTG | T | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.433+605_433+609del others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 26639434 | ||||||
| chr4:26639496 | G | T | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-645G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639496 | |||||||
| chr4:26639560 | T | G | 1 | a0001c0002t0002g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.434-581T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639560 | |||||||
| chr4:26639646 | A | G | 1 | a0001c0003t0001g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.434-495A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639646 | |||||||
| chr4:26639862 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0046 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.434-279A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639862 | |||||||
| chr4:26640129 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.434-12A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26640129 | |||||||
| chr4:26640366 | A | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+179A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640366 | |||||||
| chr4:26640450 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+263G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640450 | |||||||
| chr4:26640587 | C | T | 2 | a0001c0002t0002g0241 a0001c0002t0002g0256 |
2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.480+400C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640587 | |||||||
| chr4:26640629 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.480+442G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640629 | |||||||
| chr4:26640752 | A | C | 1 | a0001c0010t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.480+565A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640752 | |||||||
| chr4:26640764 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+577T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640764 | |||||||
| chr4:26640788 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.480+601A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640788 | |||||||
| chr4:26640810 | C | T | 1 | a0001c0002t0002g0255 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.480+623C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640810 | |||||||
| chr4:26640846 | G | T | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.480+659G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640846 | |||||||
| chr4:26640892 | C | T | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+705C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640892 | |||||||
| chr4:26640932 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+745A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640932 | |||||||
| chr4:26641003 | CT | C | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0125 others(3): Show |
6 | HG00609.hp1 NA18986.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+817delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641003 | |||||||
| chr4:26641028 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0083 others(1): Show |
4 | HG00280.hp1 HG01981.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+841G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641028 | |||||||
| chr4:26641073 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+886C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641073 | |||||||
| chr4:26641114 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+927C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641114 | |||||||
| chr4:26641118 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+931C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641118 | |||||||
| chr4:26641247 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0009g0175 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.480+1060T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641247 | |||||||
| chr4:26641310 | T | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+1123T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641310 | |||||||
| chr4:26641532 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480+1345C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641532 | |||||||
| chr4:26641533 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1346G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641533 | |||||||
| chr4:26641631 | GA | G | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.480+1445delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641631 | |||||||
| chr4:26641800 | G | A | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+1613G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641800 | |||||||
| chr4:26641873 | T | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.480+1686T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641873 | |||||||
| chr4:26641954 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.480+1767T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641954 | |||||||
| chr4:26642145 | A | G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+1958A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642145 | |||||||
| chr4:26642335 | C | T | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2148C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642335 | |||||||
| chr4:26642366 | G | T | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2179G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642366 | |||||||
| chr4:26642424 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.480+2237G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642424 | |||||||
| chr4:26642458 | C | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.480+2271C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642458 | |||||||
| chr4:26642766 | G | A | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.480+2579G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642766 | |||||||
| chr4:26642828 | CAAAG | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.480+2644_480+2647d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26642828 | ||||||
| chr4:26642834 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.480+2647A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642834 | |||||||
| chr4:26642850 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.480+2663G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642850 | |||||||
| chr4:26643012 | G | C | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.480+2825G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643012 | |||||||
| chr4:26643068 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.480+2881C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643068 | |||||||
| chr4:26643187 | C | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+3000C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643187 | |||||||
| chr4:26643285 | G | A | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.480+3098G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643285 | |||||||
| chr4:26643345 | T | C | 1 | a0001c0002t0002g0287 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.480+3158T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643345 | |||||||
| chr4:26643365 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+3178C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643365 | |||||||
| chr4:26643412 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.480+3225G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643412 | |||||||
| chr4:26643435 | G | A | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+3248G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643435 | |||||||
| chr4:26643573 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.480+3386G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643573 | |||||||
| chr4:26643603 | A | C | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3416A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643603 | |||||||
| chr4:26643611 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+3424C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643611 | |||||||
| chr4:26643627 | T | C | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.480+3440T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643627 | |||||||
| chr4:26643846 | C | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.480+3659C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643846 | |||||||
| chr4:26643921 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480+3734G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643921 | |||||||
| chr4:26643961 | C | T | 3 | a0001c0002t0002g0235 a0001c0002t0002g0240 a0001c0002t0002g0270 |
3 | HG02135.hp2 HG02165.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.480+3774C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643961 | |||||||
| chr4:26643973 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.480+3786A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643973 | |||||||
| chr4:26643997 | A | G | 9 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+3810A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643997 | |||||||
| chr4:26644087 | A | T | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+3900A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644087 | |||||||
| chr4:26644147 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.480+3960C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644147 | |||||||
| chr4:26644156 | T | C | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+3969T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644156 | |||||||
| chr4:26644175 | T | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+3988T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644175 | |||||||
| chr4:26644235 | C | T | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.480+4048C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644235 | |||||||
| chr4:26644237 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.480+4050G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644237 | |||||||
| chr4:26644412 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.480+4225G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644412 | |||||||
| chr4:26644477 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+4290G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644477 | |||||||
| chr4:26644531 | C | G | 1 | a0001c0002t0002g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.480+4344C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644531 | |||||||
| chr4:26644691 | A | G | 1 | a0001c0002t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.480+4504A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644691 | |||||||
| chr4:26644743 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.480+4556T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644743 | |||||||
| chr4:26644925 | ACACAAAC others(75): Show |
A | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+4817_480+4898d others(84): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26644925 | ||||||
| chr4:26645180 | A | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+4993A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645180 | |||||||
| chr4:26645186 | C | T | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+4999C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645186 | |||||||
| chr4:26645288 | T | TACTGGTA others(8): Show |
1 | a0001c0001t0001g0107 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.480+5102_480+5116d others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26645288 | ||||||
| chr4:26645309 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.480+5122G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645309 | |||||||
| chr4:26645568 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480+5381G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645568 | |||||||
| chr4:26645594 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480+5407G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645594 | |||||||
| chr4:26645607 | C | T | 1 | a0001c0002t0002g0291 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.480+5420C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645607 | |||||||
| chr4:26645611 | T | C | 1 | a0001c0002t0002g0291 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.480+5424T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645611 | |||||||
| chr4:26645687 | G | A | 1 | a0001c0002t0002g0242 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.480+5500G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645687 | |||||||
| chr4:26645849 | C | T | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.480+5662C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645849 | |||||||
| chr4:26645850 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.480+5663G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645850 | |||||||
| chr4:26645859 | C | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+5672C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645859 | |||||||
| chr4:26645860 | A | C | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+5673A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645860 | |||||||
| chr4:26645861 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.480+5674C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645861 | |||||||
| chr4:26645889 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.480+5702C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645889 | |||||||
| chr4:26645890 | G | A | 1 | a0001c0002t0002g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.480+5703G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645890 | |||||||
| chr4:26645919 | C | T | 2 | a0001c0002t0002g0241 a0001c0002t0002g0256 |
2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.480+5732C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645919 | |||||||
| chr4:26645923 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.480+5736A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645923 | |||||||
| chr4:26645995 | C | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+5808C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645995 | |||||||
| chr4:26645996 | G | A | 1 | a0001c0002t0002g0288 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.480+5809G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645996 | |||||||
| chr4:26646079 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.480+5892C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646079 | |||||||
| chr4:26646122 | C | CA | 34 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0069 others(31): Show |
34 | HG00544.hp1 HG00673.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.480+5957dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26646122 | ||||||
| chr4:26646122 | CA | C | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(6): Show |
9 | HG01168.hp2 HG02015.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+5957delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26646122 | ||||||
| chr4:26646233 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.480+6046A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646233 | |||||||
| chr4:26646464 | A | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+6277A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646464 | |||||||
| chr4:26646511 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.480+6324A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646511 | |||||||
| chr4:26646525 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.480+6338C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646525 | |||||||
| chr4:26646647 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+6460A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646647 | |||||||
| chr4:26646827 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.480+6640C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646827 | |||||||
| chr4:26646845 | TTAATGAG others(7): Show |
T | 1 | a0001c0001t0001g0107 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.480+6659_480+6672d others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646845 | |||||||
| chr4:26646868 | C | T | 1 | a0001c0003t0001g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.480+6681C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646868 | |||||||
| chr4:26647368 | T | A | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+7181T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647368 | |||||||
| chr4:26647465 | A | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+7278A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647465 | |||||||
| chr4:26647537 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+7350C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647537 | |||||||
| chr4:26647739 | C | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.480+7552C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647739 | |||||||
| chr4:26647943 | T | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+7756T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647943 | |||||||
| chr4:26648418 | T | C | 1 | a0001c0004t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.480+8231T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648418 | |||||||
| chr4:26648442 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.480+8255C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648442 | |||||||
| chr4:26648468 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+8281G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648468 | |||||||
| chr4:26648491 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.480+8304G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648491 | |||||||
| chr4:26648884 | C | G | 31 | a0001c0002t0002g0154 a0001c0002t0002g0212 a0001c0002t0002g0272 others(28): Show |
31 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.480+8697C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648884 | |||||||
| chr4:26649150 | A | AT | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.480+8971dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26649150 | ||||||
| chr4:26649507 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.480+9320A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649507 | |||||||
| chr4:26649630 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.480+9443T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649630 | |||||||
| chr4:26649635 | A | G | 8 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(5): Show |
8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+9448A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649635 | |||||||
| chr4:26649722 | T | A | 2 | a0001c0001t0001g0168 a0001c0001t0008g0209 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.480+9535T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649722 | |||||||
| chr4:26649760 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.480+9573G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649760 | |||||||
| chr4:26649767 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.480+9580T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649767 | |||||||
| chr4:26649769 | T | A | 1 | a0001c0002t0002g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.480+9582T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649769 | |||||||
| chr4:26649780 | T | C | 1 | a0001c0005t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.480+9593T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649780 | |||||||
| chr4:26649847 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480+9660T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649847 | |||||||
| chr4:26649876 | C | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+9689C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649876 | |||||||
| chr4:26649918 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.481-9679C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649918 | |||||||
| chr4:26649919 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.481-9678A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649919 | |||||||
| chr4:26649943 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-9654A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649943 | |||||||
| chr4:26649967 | GT | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.481-9624delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26649967 | ||||||
| chr4:26650009 | A | G | 4 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-9588A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650009 | |||||||
| chr4:26650018 | C | T | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-9579C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650018 | |||||||
| chr4:26650021 | A | G | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.481-9576A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650021 | |||||||
| chr4:26650098 | A | T | 2 | a0001c0002t0002g0289 a0001c0002t0002g0290 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.481-9499A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650098 | |||||||
| chr4:26650105 | A | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.481-9492A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650105 | |||||||
| chr4:26650195 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.481-9402C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650195 | |||||||
| chr4:26650217 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.481-9380A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650217 | |||||||
| chr4:26650228 | C | A | 2 | a0001c0001t0001g0167 a0001c0002t0002g0240 |
2 | HG01261.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.481-9369C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650228 | |||||||
| chr4:26650236 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.481-9361A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650236 | |||||||
| chr4:26650319 | A | C | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.481-9278A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650319 | |||||||
| chr4:26650320 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.481-9277G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650320 | |||||||
| chr4:26650401 | C | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-9196C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650401 | |||||||
| chr4:26650645 | T | G | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | NA18957.hp1 NA18964.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.481-8952T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650645 | |||||||
| chr4:26650711 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481-8886T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650711 | |||||||
| chr4:26650871 | C | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.481-8726C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650871 | |||||||
| chr4:26650901 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.481-8696A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650901 | |||||||
| chr4:26650936 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.481-8661T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650936 | |||||||
| chr4:26650956 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.481-8641C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650956 | |||||||
| chr4:26650990 | G | T | 110 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.481-8607G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650990 | |||||||
| chr4:26651022 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.481-8575T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651022 | |||||||
| chr4:26651091 | G | C | 2 | a0001c0001t0001g0149 a0001c0001t0003g0197 |
2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.481-8506G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651091 | |||||||
| chr4:26651124 | T | A | 1 | a0001c0002t0002g0273 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.481-8473T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651124 | |||||||
| chr4:26651148 | G | A | 1 | a0001c0002t0002g0268 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.481-8449G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651148 | |||||||
| chr4:26651151 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481-8446A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651151 | |||||||
| chr4:26651159 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.481-8438G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651159 | |||||||
| chr4:26651174 | G | C | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.481-8423G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651174 | |||||||
| chr4:26651351 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.481-8246T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651351 | |||||||
| chr4:26651436 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.481-8161C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651436 | |||||||
| chr4:26651573 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481-8024C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651573 | |||||||
| chr4:26651574 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481-8023C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651574 | |||||||
| chr4:26651620 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.481-7977G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651620 | |||||||
| chr4:26651762 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-7835G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651762 | |||||||
| chr4:26651763 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-7834G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651763 | |||||||
| chr4:26651788 | G | A | 1 | a0001c0002t0002g0235 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.481-7809G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651788 | |||||||
| chr4:26651868 | T | C | 31 | a0001c0002t0002g0154 a0001c0002t0002g0212 a0001c0002t0002g0272 others(28): Show |
31 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.481-7729T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651868 | |||||||
| chr4:26652225 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.481-7372T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652225 | |||||||
| chr4:26652243 | G | GGATTCCC others(328): Show |
1 | a0001c0001t0001g0109 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(337): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | ||||||
| chr4:26652243 | G | GGATTCCC others(337): Show |
1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.481-7338_481-7337i others(346): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | ||||||
| chr4:26652243 | G | GGATTCCC others(338): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0096 |
2 | HG00621.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.481-7338_481-7337i others(347): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | ||||||
| chr4:26652243 | G | GGATTCCC others(339): Show |
1 | a0001c0001t0001g0077 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(348): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | ||||||
| chr4:26652243 | G | GGATTCCC others(340): Show |
1 | a0001c0005t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(349): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | ||||||
| chr4:26652243 | G | GGATTCCC others(341): Show |
1 | a0001c0005t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(350): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | ||||||
| chr4:26652273 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.481-7324G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652273 | |||||||
| chr4:26652311 | T | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(2): Show |
5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-7286T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652311 | |||||||
| chr4:26652348 | T | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0016 others(14): Show |
17 | HG00609.hp2 HG00673.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.481-7249T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652348 | |||||||
| chr4:26652659 | G | A | 106 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.481-6938G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652659 | |||||||
| chr4:26652699 | G | T | 1 | a0001c0003t0001g0011 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.481-6898G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652699 | |||||||
| chr4:26652788 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-6809A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652788 | |||||||
| chr4:26652845 | G | T | 1 | a0001c0005t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481-6752G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652845 | |||||||
| chr4:26652904 | G | T | 101 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.481-6693G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652904 | |||||||
| chr4:26652959 | T | A | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-6638T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652959 | |||||||
| chr4:26653117 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-6480C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653117 | |||||||
| chr4:26653201 | C | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | NA18948.hp1 NA18995.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.481-6396C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653201 | |||||||
| chr4:26653315 | G | A | 1 | a0001c0004t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.481-6282G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653315 | |||||||
| chr4:26653472 | G | T | 1 | a0001c0003t0001g0026 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.481-6125G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653472 | |||||||
| chr4:26653713 | T | G | 3 | a0001c0002t0002g0255 a0001c0002t0002g0257 a0001c0002t0002g0259 |
3 | HG00099.hp1 HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.481-5884T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653713 | |||||||
| chr4:26653714 | C | T | 3 | a0001c0002t0002g0255 a0001c0002t0002g0257 a0001c0002t0002g0259 |
3 | HG00099.hp1 HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.481-5883C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653714 | |||||||
| chr4:26653762 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-5835T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653762 | |||||||
| chr4:26653763 | G | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-5834G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653763 | |||||||
| chr4:26653801 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.481-5796C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653801 | |||||||
| chr4:26653963 | T | C | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.481-5634T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653963 | |||||||
| chr4:26653988 | C | G | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-5609C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653988 | |||||||
| chr4:26653991 | C | T | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-5606C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653991 | |||||||
| chr4:26654013 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.481-5584G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654013 | |||||||
| chr4:26654028 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0187 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.481-5569T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654028 | |||||||
| chr4:26654080 | A | T | 11 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(8): Show |
11 | HG00733.hp1 HG02630.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-5517A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654080 | |||||||
| chr4:26654100 | A | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.481-5497A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654100 | |||||||
| chr4:26654131 | A | G | 1 | a0001c0002t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.481-5466A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654131 | |||||||
| chr4:26654162 | G | C | 111 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.481-5435G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654162 | |||||||
| chr4:26654270 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.481-5327T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654270 | |||||||
| chr4:26654307 | T | C | 3 | a0001c0002t0002g0272 a0001c0002t0002g0292 a0001c0002t0002g0294 |
3 | HG01256.hp2 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.481-5290T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654307 | |||||||
| chr4:26654464 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.481-5133A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654464 | |||||||
| chr4:26654512 | A | T | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-5085A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654512 | |||||||
| chr4:26654690 | C | T | 1 | a0001c0002t0002g0265 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.481-4907C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654690 | |||||||
| chr4:26654729 | G | A | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-4868G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654729 | |||||||
| chr4:26654762 | T | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-4835T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654762 | |||||||
| chr4:26654872 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.481-4725T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654872 | |||||||
| chr4:26654875 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.481-4722A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654875 | |||||||
| chr4:26654896 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-4701G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654896 | |||||||
| chr4:26654901 | T | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-4696T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654901 | |||||||
| chr4:26655145 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.481-4452C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655145 | |||||||
| chr4:26655153 | C | A | 1 | a0001c0002t0002g0233 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.481-4444C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655153 | |||||||
| chr4:26655168 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.481-4429C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655168 | |||||||
| chr4:26655178 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.481-4419G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655178 | |||||||
| chr4:26655179 | G | C | 1 | a0001c0002t0002g0228 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.481-4418G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655179 | |||||||
| chr4:26655254 | C | T | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.481-4343C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655254 | |||||||
| chr4:26655255 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0003g0195 |
2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481-4342G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655255 | |||||||
| chr4:26655260 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.481-4337T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655260 | |||||||
| chr4:26655305 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.481-4292G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655305 | |||||||
| chr4:26655356 | A | T | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-4241A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655356 | |||||||
| chr4:26655413 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.481-4184A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655413 | |||||||
| chr4:26655439 | C | T | 1 | a0001c0002t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.481-4158C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655439 | |||||||
| chr4:26655452 | G | A | 1 | a0001c0001t0007g0029 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.481-4145G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655452 | |||||||
| chr4:26655560 | C | T | 3 | a0001c0002t0002g0282 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.481-4037C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655560 | |||||||
| chr4:26655561 | G | A | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-4036G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655561 | |||||||
| chr4:26655655 | A | T | 1 | a0001c0002t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.481-3942A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655655 | |||||||
| chr4:26655664 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.481-3933T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655664 | |||||||
| chr4:26655838 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481-3759G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655838 | |||||||
| chr4:26655891 | TC | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0010t0001g0034 |
3 | HG02615.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.481-3704delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26655891 | ||||||
| chr4:26655958 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-3639G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655958 | |||||||
| chr4:26655966 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-3631C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655966 | |||||||
| chr4:26655975 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-3622C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655975 | |||||||
| chr4:26655981 | A | T | 4 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0110 others(1): Show |
4 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-3616A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655981 | |||||||
| chr4:26656039 | G | GT | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.481-3549dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656039 | ||||||
| chr4:26656141 | A | G | 1 | a0002c0007t0001g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.481-3456A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656141 | |||||||
| chr4:26656145 | A | G | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-3452A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656145 | |||||||
| chr4:26656202 | T | C | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-3395T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656202 | |||||||
| chr4:26656506 | C | T | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-3091C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656506 | |||||||
| chr4:26656513 | A | G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-3084A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656513 | |||||||
| chr4:26656622 | A | G | 5 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0001c0001t0009g0175 others(2): Show |
5 | HG02451.hp1 HG03017.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2975A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656622 | |||||||
| chr4:26656623 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.481-2974A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656623 | |||||||
| chr4:26656637 | T | C | 5 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0001c0001t0009g0175 others(2): Show |
5 | HG02451.hp1 HG03017.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2960T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656637 | |||||||
| chr4:26656653 | G | A | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.481-2944G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656653 | |||||||
| chr4:26656758 | G | A | 20 | a0001c0002t0002g0154 a0001c0002t0002g0272 a0001c0002t0002g0281 others(17): Show |
20 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.481-2839G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656758 | |||||||
| chr4:26656774 | G | C | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481-2823G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656774 | |||||||
| chr4:26656857 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.481-2740A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656857 | |||||||
| chr4:26656859 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481-2738A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656859 | |||||||
| chr4:26656958 | T | TTTC | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2607_481-2605d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656958 | ||||||
| chr4:26656981 | T | TCTCCTTC others(8): Show |
1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.481-2614_481-2613i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | ||||||
| chr4:26656981 | T | TCTTCTCC others(17): Show |
1 | a0001c0002t0002g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.481-2611_481-2610i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | ||||||
| chr4:26656981 | T | TCTTCTCC others(53): Show |
1 | a0003c0008t0006g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.481-2611_481-2610i others(62): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | ||||||
| chr4:26656981 | T | TCTTCTCC others(65): Show |
1 | a0003c0008t0006g0115 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.481-2611_481-2610i others(74): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | ||||||
| chr4:26656981 | TCTTCTTC others(5): Show |
T | 1 | a0001c0001t0001g0120 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.481-2610_481-2599d others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | ||||||
| chr4:26656987 | T | C | 16 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0123 others(13): Show |
16 | HG01496.hp1 HG02145.hp2 HG03017.hp1 others(13): Show |
intron_variant | MODIFIER | c.481-2610T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656987 | |||||||
| chr4:26656987 | T | TCTC | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(8): Show |
12 | HG00609.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTCCTTC others(2): Show |
12 | a0001c0001t0001g0128 a0001c0001t0002g0152 a0001c0002t0002g0216 others(9): Show |
12 | HG00642.hp2 HG00741.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(11): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTCCTTC others(8): Show |
18 | a0001c0002t0002g0217 a0001c0002t0002g0232 a0001c0002t0002g0233 others(15): Show |
18 | HG00280.hp2 HG00544.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTCCTTC others(14): Show |
44 | a0001c0001t0002g0116 a0001c0001t0002g0153 a0001c0002t0002g0203 others(41): Show |
44 | HG00099.hp1 HG00140.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(23): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTCCTTC others(20): Show |
12 | a0001c0002t0002g0272 a0001c0002t0002g0274 a0001c0002t0002g0275 others(9): Show |
12 | HG01256.hp2 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTCCTTC others(26): Show |
7 | a0001c0002t0002g0213 a0001c0002t0002g0282 a0001c0002t0002g0286 others(4): Show |
7 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTCCTTC others(32): Show |
5 | a0001c0002t0002g0154 a0001c0002t0002g0281 a0001c0002t0002g0285 others(2): Show |
5 | HG03710.hp1 NA18963.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTC | 5 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(2): Show |
5 | HG01884.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2567_481-2562d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTCC others(5): Show |
1 | a0001c0001t0002g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.481-2573_481-2562d others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTCC others(11): Show |
4 | a0001c0001t0003g0195 a0001c0002t0002g0200 a0001c0002t0002g0201 others(1): Show |
4 | HG02886.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2579_481-2562d others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTCC others(23): Show |
2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.481-2591_481-2562d others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTCC others(29): Show |
1 | a0001c0002t0002g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.481-2597_481-2562d others(38): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(8): Show |
1 | a0001c0002t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(20): Show |
1 | a0001c0002t0002g0228 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(26): Show |
3 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 |
3 | HG02976.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(11): Show |
1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(17): Show |
4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(8): Show |
1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(14): Show |
10 | a0001c0001t0001g0086 a0001c0001t0001g0111 a0001c0001t0001g0168 others(7): Show |
10 | HG01243.hp2 HG02258.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(23): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(20): Show |
1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(26): Show |
2 | a0001c0001t0001g0052 a0004c0009t0001g0108 |
2 | NA19064.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(32): Show |
2 | a0001c0001t0001g0004 a0001c0003t0001g0043 |
2 | HG02015.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(38): Show |
1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(17): Show |
1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(23): Show |
2 | a0001c0001t0001g0021 a0001c0001t0003g0196 |
2 | HG03486.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(29): Show |
5 | a0001c0001t0001g0049 a0001c0001t0001g0078 a0001c0001t0001g0083 others(2): Show |
5 | HG01261.hp1 HG02293.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(38): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(35): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0100 |
3 | HG02818.hp2 HG02886.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(44): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(41): Show |
2 | a0001c0001t0001g0074 a0001c0001t0007g0030 |
2 | HG02083.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(20): Show |
3 | a0001c0001t0001g0171 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02976.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(26): Show |
8 | a0001c0001t0001g0149 a0001c0001t0001g0172 a0001c0001t0001g0185 others(5): Show |
8 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(32): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0056 others(2): Show |
5 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(38): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0087 a0001c0005t0001g0105 others(2): Show |
5 | HG00544.hp2 HG01069.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(44): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0007g0029 |
3 | HG01993.hp2 NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(17): Show |
1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(23): Show |
5 | a0001c0001t0001g0081 a0001c0001t0001g0181 a0001c0001t0001g0186 others(2): Show |
5 | HG00323.hp1 HG00733.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(29): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0053 others(5): Show |
8 | HG01358.hp2 HG01934.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(38): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(35): Show |
11 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0050 others(8): Show |
11 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(44): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(41): Show |
10 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0063 others(7): Show |
10 | HG00621.hp2 HG02071.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(47): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0093 others(1): Show |
4 | HG02135.hp1 HG02165.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(56): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(59): Show |
1 | a0001c0001t0001g0076 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(68): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(65): Show |
1 | a0001c0001t0001g0045 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(74): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(20): Show |
1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(26): Show |
2 | a0001c0001t0001g0173 a0001c0001t0003g0197 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(32): Show |
1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(38): Show |
8 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0064 others(5): Show |
8 | HG00140.hp1 HG00673.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(44): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG00738.hp2 HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(50): Show |
1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(59): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(23): Show |
3 | a0001c0001t0001g0033 a0001c0001t0008g0148 a0001c0001t0008g0209 |
3 | HG00642.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(35): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0066 |
2 | HG00280.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(44): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(41): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0037 others(4): Show |
7 | HG02155.hp1 HG03927.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(47): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0072 |
3 | HG01496.hp2 HG03490.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(56): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(26): Show |
1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(44): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0055 |
2 | HG02683.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(50): Show |
8 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0044 others(5): Show |
8 | HG00609.hp2 HG00735.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(59): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(56): Show |
2 | a0001c0001t0001g0047 a0001c0001t0004g0036 |
2 | HG02895.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(65): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(41): Show |
1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(47): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0097 others(2): Show |
5 | HG02080.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(56): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(53): Show |
2 | a0001c0001t0001g0005 a0001c0001t0004g0038 |
2 | HG00639.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(62): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(38): Show |
1 | a0001c0001t0001g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(56): Show |
1 | a0001c0001t0004g0023 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(65): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(53): Show |
1 | a0001c0001t0001g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(62): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(44): Show |
1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26656987 | T | TCTTCTTC others(65): Show |
1 | a0001c0005t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(74): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | ||||||
| chr4:26657033 | C | CTCCT | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2562_481-2561i others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657033 | ||||||
| chr4:26657053 | CTTG | C | 3 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0001c0002t0002g0277 |
3 | HG02451.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.481-2541_481-2539d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657053 | ||||||
| chr4:26657056 | G | GTTC | 15 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(12): Show |
15 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.481-2519_481-2517d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657056 | ||||||
| chr4:26657056 | G | GTTCTTC | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0168 others(1): Show |
4 | HG02559.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2522_481-2517d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657056 | ||||||
| chr4:26657056 | GTTC | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.481-2519_481-2517d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657056 | ||||||
| chr4:26657191 | C | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.481-2406C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657191 | |||||||
| chr4:26657483 | G | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2114G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657483 | |||||||
| chr4:26657487 | T | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2110T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657487 | |||||||
| chr4:26657488 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2109A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657488 | |||||||
| chr4:26657492 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2105G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657492 | |||||||
| chr4:26657592 | T | C | 1 | a0001c0002t0002g0262 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.481-2005T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657592 | |||||||
| chr4:26658043 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-1554C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658043 | |||||||
| chr4:26658053 | A | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-1544A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658053 | |||||||
| chr4:26658218 | A | T | 1 | a0001c0002t0010g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.481-1379A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658218 | |||||||
| chr4:26658489 | G | A | 4 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0003c0008t0006g0114 others(1): Show |
4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-1108G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658489 | |||||||
| chr4:26658519 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-1078G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658519 | |||||||
| chr4:26658536 | G | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.481-1061G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658536 | |||||||
| chr4:26658567 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.481-1030C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658567 | |||||||
| chr4:26658611 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18948.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.481-986C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658611 | |||||||
| chr4:26658790 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.481-807A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658790 | |||||||
| chr4:26658840 | G | A | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.481-757G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658840 | |||||||
| chr4:26658842 | G | A | 5 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0001c0001t0009g0175 others(2): Show |
5 | HG02451.hp1 HG03017.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-755G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658842 | |||||||
| chr4:26658897 | G | T | 1 | a0001c0002t0002g0154 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.481-700G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658897 | |||||||
| chr4:26658989 | G | A | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-608G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658989 | |||||||
| chr4:26658991 | C | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-606C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658991 | |||||||
| chr4:26659051 | C | A | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481-546C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659051 | |||||||
| chr4:26659072 | A | T | 1 | a0003c0008t0006g0115 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.481-525A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659072 | |||||||
| chr4:26659221 | T | A | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481-376T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659221 | |||||||
| chr4:26659398 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481-199C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659398 | |||||||
| chr4:26659729 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.591+22T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26659729 | |||||||
| chr4:26659762 | T | G | 1 | a0001c0003t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.591+55T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26659762 | |||||||
| chr4:26659988 | C | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.591+281C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26659988 | |||||||
| chr4:26660254 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.591+547C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660254 | |||||||
| chr4:26660264 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.591+557A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660264 | |||||||
| chr4:26660365 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.591+658C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660365 | |||||||
| chr4:26660518 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.591+811G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660518 | |||||||
| chr4:26660782 | C | T | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+1075C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660782 | |||||||
| chr4:26660784 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | NA18944.hp1 NA18972.hp1 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+1077C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660784 | |||||||
| chr4:26661129 | T | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.591+1422T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661129 | |||||||
| chr4:26661203 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.591+1496C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661203 | |||||||
| chr4:26661215 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.591+1508A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661215 | |||||||
| chr4:26661517 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.591+1810C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661517 | |||||||
| chr4:26661522 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.591+1815C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661522 | |||||||
| chr4:26661708 | G | C | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+2001G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661708 | |||||||
| chr4:26661816 | C | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.591+2109C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661816 | |||||||
| chr4:26662145 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.591+2438T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662145 | |||||||
| chr4:26662245 | C | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.591+2538C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662245 | |||||||
| chr4:26662347 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0180 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.591+2640A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662347 | |||||||
| chr4:26662401 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.591+2694T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662401 | |||||||
| chr4:26662455 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.591+2748C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662455 | |||||||
| chr4:26662832 | T | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.591+3125T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662832 | |||||||
| chr4:26662972 | A | G | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.591+3265A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662972 | |||||||
| chr4:26663003 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.591+3296C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663003 | |||||||
| chr4:26663051 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.592-3282G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663051 | |||||||
| chr4:26663155 | A | G | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592-3178A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663155 | |||||||
| chr4:26663810 | T | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-2523T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663810 | |||||||
| chr4:26664059 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.592-2274C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664059 | |||||||
| chr4:26664444 | G | T | 1 | a0001c0002t0002g0293 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.592-1889G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664444 | |||||||
| chr4:26664483 | T | C | 1 | a0001c0002t0002g0296 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.592-1850T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664483 | |||||||
| chr4:26664576 | A | G | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.592-1757A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664576 | |||||||
| chr4:26664628 | CT | C | 6 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG00733.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-1689delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | 26664628 | ||||||
| chr4:26664724 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592-1609C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664724 | |||||||
| chr4:26664873 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.592-1460G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664873 | |||||||
| chr4:26664997 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1336C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664997 | |||||||
| chr4:26665028 | G | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(21): Show |
24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.592-1305G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665028 | |||||||
| chr4:26665066 | G | C | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-1267G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665066 | |||||||
| chr4:26665095 | G | T | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.592-1238G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665095 | |||||||
| chr4:26665147 | G | T | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592-1186G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665147 | |||||||
| chr4:26665264 | T | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0180 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.592-1069T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665264 | |||||||
| chr4:26665415 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.592-918C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665415 | |||||||
| chr4:26665515 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.592-818A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665515 | |||||||
| chr4:26665916 | A | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.592-417A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665916 | |||||||
| chr4:26665997 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.592-336A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665997 | |||||||
| chr4:26666706 | ATC | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+303_664+304del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26666706 | ||||||
| chr4:26666722 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.664+317G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666722 | |||||||
| chr4:26666765 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.664+360C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666765 | |||||||
| chr4:26666808 | G | A | 1 | a0001c0002t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.664+403G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666808 | |||||||
| chr4:26666842 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.664+437A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666842 | |||||||
| chr4:26666849 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.664+444A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666849 | |||||||
| chr4:26667062 | G | A | 3 | a0001c0002t0002g0300 a0001c0002t0002g0301 a0001c0002t0002g0302 |
3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.664+657G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667062 | |||||||
| chr4:26667274 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664+869A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667274 | |||||||
| chr4:26667281 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+876A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667281 | |||||||
| chr4:26667353 | C | G | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.664+948C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667353 | |||||||
| chr4:26667569 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.664+1164C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667569 | |||||||
| chr4:26667576 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.664+1171T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667576 | |||||||
| chr4:26667663 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.664+1258A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667663 | |||||||
| chr4:26667680 | C | T | 1 | a0001c0002t0002g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.664+1275C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667680 | |||||||
| chr4:26667725 | C | G | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.664+1320C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667725 | |||||||
| chr4:26668012 | G | A | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.664+1607G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668012 | |||||||
| chr4:26668287 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0085 |
3 | HG00738.hp2 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.664+1882C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668287 | |||||||
| chr4:26668459 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+2054C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668459 | |||||||
| chr4:26668744 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0082 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.664+2339G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668744 | |||||||
| chr4:26668986 | T | TAC | 13 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0160 others(10): Show |
13 | HG01261.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.664+2615_664+2616d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | T | TACAC | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0176 others(4): Show |
7 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+2613_664+2616d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | T | TACACAC | 25 | a0001c0001t0001g0009 a0001c0001t0001g0117 a0001c0001t0001g0118 others(22): Show |
25 | HG02257.hp2 HG02976.hp2 HG03471.hp2 others(22): Show |
intron_variant | MODIFIER | c.664+2611_664+2616d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0171 others(6): Show |
9 | HG00609.hp1 HG00733.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.664+2609_664+2616d others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0129 a0002c0007t0001g0163 a0002c0007t0001g0164 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+2607_664+2616d others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | T | TACACACA others(5): Show |
2 | a0001c0001t0001g0185 a0002c0007t0001g0165 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.664+2605_664+2616d others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | TAC | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.664+2615_664+2616d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | TACAC | T | 38 | a0001c0001t0001g0047 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.664+2613_664+2616d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26668986 | TACACAC | T | 76 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(73): Show |
76 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.664+2611_664+2616d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | ||||||
| chr4:26669335 | A | G | 32 | a0001c0001t0002g0019 a0001c0002t0002g0001 a0001c0002t0002g0216 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.665-2814A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669335 | |||||||
| chr4:26669353 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.665-2796A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669353 | |||||||
| chr4:26669602 | T | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(8): Show |
11 | NA18941.hp1 NA18946.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-2547T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669602 | |||||||
| chr4:26669770 | A | G | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-2379A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669770 | |||||||
| chr4:26669801 | G | A | 1 | a0001c0002t0002g0291 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.665-2348G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669801 | |||||||
| chr4:26670340 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.665-1809A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670340 | |||||||
| chr4:26670376 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.665-1773A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670376 | |||||||
| chr4:26670446 | A | G | 1 | a0001c0001t0004g0023 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.665-1703A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670446 | |||||||
| chr4:26670518 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0001g0096 others(2): Show |
5 | HG00621.hp2 NA18964.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-1631A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670518 | |||||||
| chr4:26670573 | T | C | 2 | a0001c0001t0001g0094 a0001c0002t0002g0252 |
2 | NA18948.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.665-1576T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670573 | |||||||
| chr4:26670606 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.665-1543C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670606 | |||||||
| chr4:26671051 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.665-1098T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671051 | |||||||
| chr4:26671351 | A | C | 36 | a0001c0001t0002g0019 a0001c0002t0002g0001 a0001c0002t0002g0200 others(33): Show |
37 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.665-798A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671351 | |||||||
| chr4:26671529 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0042 |
2 | HG00140.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.665-620T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671529 | |||||||
| chr4:26671548 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.665-601A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671548 | |||||||
| chr4:26671790 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-359A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671790 | |||||||
| chr4:26671957 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.665-192A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671957 | |||||||
| chr4:26672139 | T | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.665-10T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26672139 | |||||||
| chr4:26672246 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+59G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672246 | |||||||
| chr4:26672411 | G | A | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+224G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672411 | |||||||
| chr4:26672450 | G | A | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+263G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672450 | |||||||
| chr4:26672451 | A | T | 1 | a0001c0003t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703+264A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672451 | |||||||
| chr4:26672469 | C | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.703+282C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672469 | |||||||
| chr4:26673206 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.704-570G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673206 | |||||||
| chr4:26673318 | T | C | 2 | a0001c0002t0002g0223 a0001c0002t0002g0224 |
2 | HG01981.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.704-458T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673318 | |||||||
| chr4:26673358 | A | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.704-418A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673358 | |||||||
| chr4:26673424 | C | CAT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(21): Show |
24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.704-330_704-329dup others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673424 | ||||||
| chr4:26673440 | T | TACACACA others(5): Show |
5 | a0001c0001t0003g0196 a0002c0007t0001g0163 a0002c0007t0001g0164 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-335_704-334ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673440 | ||||||
| chr4:26673440 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.704-335_704-334ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673440 | ||||||
| chr4:26673442 | T | C | 6 | a0001c0001t0001g0162 a0001c0001t0003g0196 a0002c0007t0001g0163 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-334T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673442 | |||||||
| chr4:26673442 | T | TACACACA others(7): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0178 |
2 | HG01261.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.704-333_704-332ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673442 | ||||||
| chr4:26673442 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-333_704-332ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673442 | ||||||
| chr4:26673444 | T | C | 14 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(11): Show |
15 | HG00735.hp1 HG01243.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-332T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673444 | |||||||
| chr4:26673444 | T | TAC | 7 | a0001c0001t0002g0019 a0001c0002t0002g0212 a0001c0002t0002g0237 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACAC | 66 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(63): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACAC | 6 | a0001c0002t0002g0275 a0001c0002t0002g0277 a0001c0002t0002g0278 others(3): Show |
6 | HG00639.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACACA others(1): Show |
17 | a0001c0001t0001g0168 a0001c0002t0002g0154 a0001c0002t0002g0281 others(14): Show |
17 | HG00323.hp2 HG01496.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACACA others(3): Show |
6 | a0001c0002t0002g0272 a0001c0002t0002g0304 a0001c0002t0002g0305 others(3): Show |
6 | HG01256.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACACA others(5): Show |
2 | a0001c0001t0001g0169 a0001c0002t0002g0282 |
2 | HG01168.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.704-331_704-330ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACACA others(9): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.704-331_704-330ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACACA others(11): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.704-331_704-330ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673444 | T | TACACACA others(15): Show |
1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.704-331_704-330ins others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | ||||||
| chr4:26673446 | T | C | 124 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0156 others(121): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.704-330T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673446 | |||||||
| chr4:26673446 | T | TACACACA others(3): Show |
2 | a0001c0002t0002g0289 a0001c0002t0002g0290 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.704-310_704-301dup others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-312_704-301dup others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TACACACA others(7): Show |
1 | a0001c0001t0008g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.704-314_704-301dup others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TACACACA others(9): Show |
5 | a0001c0001t0008g0209 a0001c0006t0001g0211 a0001c0006t0005g0147 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-316_704-301dup others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATACACA others(5): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0149 a0001c0005t0001g0102 |
3 | HG00642.hp1 HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATACACA others(9): Show |
2 | a0001c0001t0001g0170 a0001c0005t0001g0190 |
2 | HG02735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATACACA others(11): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0185 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATACA others(5): Show |
1 | a0001c0001t0001g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.704-329_704-328ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATACA others(7): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0044 others(3): Show |
6 | HG02015.hp2 NA18955.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATACA others(9): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(14): Show |
17 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATACA others(11): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0184 a0001c0010t0001g0034 |
3 | HG02615.hp2 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATACA others(13): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0186 |
2 | HG00733.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(5): Show |
5 | a0001c0001t0001g0048 a0001c0001t0003g0192 a0001c0001t0003g0197 others(2): Show |
5 | HG02083.hp1 HG03225.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(7): Show |
4 | a0001c0001t0001g0081 a0001c0001t0003g0195 a0001c0003t0001g0011 others(1): Show |
4 | HG00323.hp1 HG02886.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(9): Show |
57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(11): Show |
8 | a0001c0001t0001g0041 a0001c0001t0001g0049 a0001c0001t0001g0075 others(5): Show |
8 | HG00621.hp2 HG02818.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(13): Show |
4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(1): Show |
4 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-329_704-328ins others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(9): Show |
3 | a0001c0001t0001g0070 a0001c0001t0003g0193 a0001c0001t0003g0194 |
3 | HG01168.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(11): Show |
7 | a0001c0001t0001g0028 a0001c0001t0001g0064 a0001c0001t0001g0083 others(4): Show |
7 | HG01981.hp1 HG02165.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0010 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-329_704-328ins others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(11): Show |
2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(13): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0110 others(1): Show |
4 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0066 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(24): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(23): Show |
2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(30): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673446 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | ||||||
| chr4:26673472 | C | CACACACA others(7): Show |
1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704-301_704-300ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673472 | ||||||
| chr4:26673472 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.704-301_704-300ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673472 | ||||||
| chr4:26674180 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0016 others(11): Show |
14 | HG00609.hp2 HG00673.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.816+292T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674180 | |||||||
| chr4:26674489 | G | C | 1 | a0001c0002t0002g0255 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.816+601G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674489 | |||||||
| chr4:26674611 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+723C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674611 | |||||||
| chr4:26674624 | C | T | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+736C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674624 | |||||||
| chr4:26674721 | G | A | 71 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(68): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.816+833G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674721 | |||||||
| chr4:26675011 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.816+1123G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675011 | |||||||
| chr4:26675065 | T | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.816+1177T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675065 | |||||||
| chr4:26675255 | G | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.816+1367G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675255 | |||||||
| chr4:26675312 | A | G | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+1424A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675312 | |||||||
| chr4:26675333 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1445G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675333 | |||||||
| chr4:26675706 | C | T | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+1818C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675706 | |||||||
| chr4:26675888 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+2000A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675888 | |||||||
| chr4:26676111 | G | A | 40 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0045 others(37): Show |
40 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.816+2223G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676111 | |||||||
| chr4:26676119 | T | C | 18 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0171 others(15): Show |
18 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+2231T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676119 | |||||||
| chr4:26676178 | A | G | 2 | a0001c0001t0002g0116 a0001c0001t0002g0152 |
2 | HG00642.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.816+2290A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676178 | |||||||
| chr4:26676379 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.816+2491T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676379 | |||||||
| chr4:26676397 | C | G | 113 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0045 others(110): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.816+2509C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676397 | |||||||
| chr4:26676418 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.816+2530T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676418 | |||||||
| chr4:26676491 | G | A | 1 | a0001c0005t0001g0103 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.816+2603G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676491 | |||||||
| chr4:26676554 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.816+2666C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676554 | |||||||
| chr4:26676577 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.816+2689G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676577 | |||||||
| chr4:26676635 | C | T | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(2): Show |
5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+2747C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676635 | |||||||
| chr4:26676636 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+2748G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676636 | |||||||
| chr4:26676675 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.816+2787C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676675 | |||||||
| chr4:26676716 | C | CA | 10 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(7): Show |
10 | HG01243.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+2845dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 26676716 | ||||||
| chr4:26676772 | C | T | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+2884C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676772 | |||||||
| chr4:26676780 | C | G | 1 | a0001c0002t0002g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.816+2892C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676780 | |||||||
| chr4:26677232 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.816+3344A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677232 | |||||||
| chr4:26677264 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816+3376A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677264 | |||||||
| chr4:26677323 | C | CT | 111 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.816+3448dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 26677323 | ||||||
| chr4:26677341 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.816+3453C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677341 | |||||||
| chr4:26677419 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0062 |
2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.816+3531C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677419 | |||||||
| chr4:26677478 | C | T | 1 | a0001c0003t0001g0043 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.816+3590C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677478 | |||||||
| chr4:26677487 | T | A | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+3599T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677487 | |||||||
| chr4:26677510 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.816+3622A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677510 | |||||||
| chr4:26677563 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.816+3675C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677563 | |||||||
| chr4:26677693 | G | T | 1 | a0001c0001t0007g0030 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.816+3805G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677693 | |||||||
| chr4:26677775 | T | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.816+3887T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677775 | |||||||
| chr4:26677813 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+3925T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677813 | |||||||
| chr4:26677976 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816+4088T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677976 | |||||||
| chr4:26678083 | A | C | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+4195A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678083 | |||||||
| chr4:26678086 | C | G | 35 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(32): Show |
35 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.816+4198C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678086 | |||||||
| chr4:26678148 | T | C | 2 | a0001c0002t0002g0289 a0001c0002t0002g0290 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.816+4260T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678148 | |||||||
| chr4:26678161 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.816+4273G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678161 | |||||||
| chr4:26678271 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+4383G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678271 | |||||||
| chr4:26678301 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.816+4413G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678301 | |||||||
| chr4:26678308 | G | A | 1 | a0001c0010t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.816+4420G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678308 | |||||||
| chr4:26678531 | T | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+4643T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678531 | |||||||
| chr4:26678539 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0180 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.816+4651T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678539 | |||||||
| chr4:26678642 | A | G | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+4754A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678642 | |||||||
| chr4:26678958 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.817-4717A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678958 | |||||||
| chr4:26679121 | C | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-4554C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679121 | |||||||
| chr4:26679182 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.817-4493G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679182 | |||||||
| chr4:26679485 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.817-4190A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679485 | |||||||
| chr4:26679600 | G | T | 1 | a0001c0001t0001g0021 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.817-4075G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679600 | |||||||
| chr4:26679692 | A | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-3983A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679692 | |||||||
| chr4:26679702 | G | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.817-3973G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679702 | |||||||
| chr4:26679724 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.817-3951C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679724 | |||||||
| chr4:26679779 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.817-3896C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679779 | |||||||
| chr4:26679819 | T | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.817-3856T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679819 | |||||||
| chr4:26679866 | C | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.817-3809C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679866 | |||||||
| chr4:26679904 | G | T | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.817-3771G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679904 | |||||||
| chr4:26680032 | G | A | 2 | a0001c0002t0002g0236 a0001c0002t0002g0250 |
2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.817-3643G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680032 | |||||||
| chr4:26680138 | A | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.817-3537A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680138 | |||||||
| chr4:26680161 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817-3514C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680161 | |||||||
| chr4:26680237 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.817-3438G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680237 | |||||||
| chr4:26680243 | G | A | 1 | a0001c0002t0002g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.817-3432G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680243 | |||||||
| chr4:26680294 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.817-3381C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680294 | |||||||
| chr4:26680361 | A | T | 33 | a0001c0001t0001g0167 a0001c0001t0002g0019 a0001c0002t0002g0001 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.817-3314A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680361 | |||||||
| chr4:26680721 | T | G | 1 | a0001c0004t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-2954T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680721 | |||||||
| chr4:26680747 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-2928C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680747 | |||||||
| chr4:26680818 | T | C | 1 | a0001c0002t0002g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.817-2857T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680818 | |||||||
| chr4:26680875 | T | G | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.817-2800T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680875 | |||||||
| chr4:26681047 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.817-2628C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681047 | |||||||
| chr4:26681173 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.817-2502G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681173 | |||||||
| chr4:26681261 | G | A | 1 | a0001c0003t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-2414G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681261 | |||||||
| chr4:26681390 | C | CA | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-2274dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 26681390 | ||||||
| chr4:26681407 | C | T | 2 | a0001c0001t0009g0175 a0001c0003t0001g0043 |
2 | HG02451.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.817-2268C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681407 | |||||||
| chr4:26681467 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.817-2208C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681467 | |||||||
| chr4:26681468 | G | A | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.817-2207G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681468 | |||||||
| chr4:26681529 | C | T | 1 | a0001c0002t0002g0278 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817-2146C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681529 | |||||||
| chr4:26681542 | C | T | 3 | a0001c0002t0002g0300 a0001c0002t0002g0301 a0001c0002t0002g0302 |
3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.817-2133C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681542 | |||||||
| chr4:26681557 | A | AT | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.817-2118_817-2117i others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681557 | |||||||
| chr4:26681559 | T | A | 7 | a0001c0001t0001g0017 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG00099.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-2116T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681559 | |||||||
| chr4:26681572 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.817-2103A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681572 | |||||||
| chr4:26681629 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.817-2046T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681629 | |||||||
| chr4:26681674 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.817-2001C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681674 | |||||||
| chr4:26681749 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.817-1926G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681749 | |||||||
| chr4:26681854 | T | A | 6 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0131 others(3): Show |
6 | NA18990.hp1 NA18994.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1821T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681854 | |||||||
| chr4:26681875 | A | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.817-1800A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681875 | |||||||
| chr4:26682313 | T | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(2): Show |
5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-1362T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682313 | |||||||
| chr4:26682455 | T | C | 1 | a0001c0002t0002g0224 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.817-1220T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682455 | |||||||
| chr4:26682489 | C | A | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.817-1186C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682489 | |||||||
| chr4:26682530 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.817-1145G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682530 | |||||||
| chr4:26682618 | G | T | 7 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
7 | HG00733.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-1057G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682618 | |||||||
| chr4:26682650 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.817-1025T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682650 | |||||||
| chr4:26682694 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.817-981C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682694 | |||||||
| chr4:26682728 | C | A | 1 | a0001c0002t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.817-947C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682728 | |||||||
| chr4:26682951 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.817-724T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682951 | |||||||
| chr4:26683126 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-549A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683126 | |||||||
| chr4:26683213 | G | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.817-462G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683213 | |||||||
| chr4:26683483 | A | G | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.817-192A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683483 | |||||||
| chr4:26683506 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.817-169A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683506 | |||||||
| chr4:26683628 | A | G | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-47A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683628 | |||||||
| chr4:26683919 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.891+170T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26683919 | |||||||
| chr4:26684096 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.891+347C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684096 | |||||||
| chr4:26684355 | C | T | 72 | a0001c0001t0001g0162 a0001c0001t0002g0019 a0001c0001t0002g0116 others(69): Show |
73 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.891+606C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684355 | |||||||
| chr4:26684456 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.891+707T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684456 | |||||||
| chr4:26684575 | T | C | 14 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(11): Show |
14 | NA18941.hp2 NA18946.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.891+826T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684575 | |||||||
| chr4:26685006 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.891+1257G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685006 | |||||||
| chr4:26685140 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.891+1391A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685140 | |||||||
| chr4:26685379 | T | C | 1 | a0001c0002t0002g0297 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.891+1630T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685379 | |||||||
| chr4:26685571 | G | A | 11 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1822G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685571 | |||||||
| chr4:26685665 | T | C | 1 | a0001c0004t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891+1916T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685665 | |||||||
| chr4:26685700 | T | C | 11 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1951T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685700 | |||||||
| chr4:26685726 | G | T | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.891+1977G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685726 | |||||||
| chr4:26685801 | T | G | 1 | a0001c0004t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891+2052T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685801 | |||||||
| chr4:26685809 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.891+2060C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685809 | |||||||
| chr4:26686016 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.891+2267C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686016 | |||||||
| chr4:26686021 | C | T | 10 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(7): Show |
10 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+2272C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686021 | |||||||
| chr4:26686085 | A | T | 1 | a0001c0006t0005g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.892-2260A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686085 | |||||||
| chr4:26686125 | A | AT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(12): Show |
15 | HG01993.hp2 HG02015.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.892-2217dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 26686125 | ||||||
| chr4:26686128 | T | TA | 7 | a0001c0001t0002g0153 a0001c0002t0002g0233 a0001c0002t0002g0305 others(4): Show |
7 | HG02015.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-2206dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 26686128 | ||||||
| chr4:26686128 | TA | T | 9 | a0001c0001t0001g0157 a0001c0001t0003g0192 a0001c0001t0003g0193 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-2206delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 26686128 | ||||||
| chr4:26686129 | A | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.892-2216A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686129 | |||||||
| chr4:26686313 | A | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-2032A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686313 | |||||||
| chr4:26686542 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0180 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.892-1803A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686542 | |||||||
| chr4:26686550 | T | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-1795T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686550 | |||||||
| chr4:26686598 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0090 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.892-1747A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686598 | |||||||
| chr4:26686811 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.892-1534C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686811 | |||||||
| chr4:26686918 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.892-1427A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686918 | |||||||
| chr4:26686933 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.892-1412A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686933 | |||||||
| chr4:26687113 | T | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-1232T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687113 | |||||||
| chr4:26687272 | T | A | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.892-1073T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687272 | |||||||
| chr4:26687544 | T | C | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.892-801T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687544 | |||||||
| chr4:26687821 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.892-524A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687821 | |||||||
| chr4:26687901 | G | A | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.892-444G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687901 | |||||||
| chr4:26687961 | T | A | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.892-384T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687961 | |||||||
| chr4:26688144 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.892-201A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26688144 | |||||||
| chr4:26688453 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.954+46C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688453 | |||||||
| chr4:26688524 | G | T | 1 | a0001c0002t0002g0292 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.954+117G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688524 | |||||||
| chr4:26688615 | G | T | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+208G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688615 | |||||||
| chr4:26688616 | TCATATAT others(4): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+213_954+223del others(11): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26688616 | ||||||
| chr4:26688660 | C | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(21): Show |
24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.954+253C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688660 | |||||||
| chr4:26688662 | A | G | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+255A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688662 | |||||||
| chr4:26688753 | T | C | 1 | a0002c0007t0001g0163 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.954+346T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688753 | |||||||
| chr4:26688753 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.954+346T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688753 | |||||||
| chr4:26688944 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.954+537T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688944 | |||||||
| chr4:26688955 | G | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+548G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688955 | |||||||
| chr4:26689147 | C | T | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.954+740C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689147 | |||||||
| chr4:26689469 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+1062T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689469 | |||||||
| chr4:26689512 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.954+1105G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689512 | |||||||
| chr4:26689526 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+1119G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689526 | |||||||
| chr4:26689568 | G | T | 1 | a0001c0002t0002g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.954+1161G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689568 | |||||||
| chr4:26689803 | A | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+1396A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689803 | |||||||
| chr4:26689830 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+1423G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689830 | |||||||
| chr4:26690369 | G | T | 1 | a0001c0001t0004g0022 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.954+1962G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690369 | |||||||
| chr4:26690407 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.954+2000A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690407 | |||||||
| chr4:26690431 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.954+2024A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690431 | |||||||
| chr4:26690718 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.954+2311C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690718 | |||||||
| chr4:26690766 | T | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+2359T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690766 | |||||||
| chr4:26690807 | A | G | 118 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(115): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.954+2400A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690807 | |||||||
| chr4:26690819 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+2412G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690819 | |||||||
| chr4:26690876 | A | C | 3 | a0001c0002t0002g0235 a0001c0002t0002g0240 a0001c0002t0002g0270 |
3 | HG02135.hp2 HG02165.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.954+2469A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690876 | |||||||
| chr4:26691383 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+2976G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691383 | |||||||
| chr4:26691415 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(20): Show |
23 | HG01257.hp1 HG01993.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.954+3008G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691415 | |||||||
| chr4:26691423 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.954+3016C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691423 | |||||||
| chr4:26691521 | C | A | 1 | a0001c0006t0005g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.954+3114C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691521 | |||||||
| chr4:26691555 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+3148C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691555 | |||||||
| chr4:26691579 | T | C | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+3172T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691579 | |||||||
| chr4:26691586 | A | AT | 11 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(8): Show |
11 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.954+3189dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26691586 | ||||||
| chr4:26691598 | G | T | 3 | a0001c0002t0002g0234 a0001c0002t0002g0236 a0001c0002t0002g0250 |
3 | NA18957.hp2 NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.954+3191G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691598 | |||||||
| chr4:26691668 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+3261T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691668 | |||||||
| chr4:26691760 | G | A | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.954+3353G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691760 | |||||||
| chr4:26692052 | G | A | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+3645G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692052 | |||||||
| chr4:26692190 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954+3783C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692190 | |||||||
| chr4:26692198 | A | G | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+3791A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692198 | |||||||
| chr4:26692312 | A | G | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.954+3905A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692312 | |||||||
| chr4:26692519 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+4112C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692519 | |||||||
| chr4:26692645 | T | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+4238T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692645 | |||||||
| chr4:26692671 | C | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.954+4264C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692671 | |||||||
| chr4:26692982 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+4575C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692982 | |||||||
| chr4:26693123 | TA | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.954+4733delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26693123 | ||||||
| chr4:26693210 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0110 a0001c0001t0001g0204 |
3 | HG00738.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.954+4803C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693210 | |||||||
| chr4:26693296 | C | T | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+4889C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693296 | |||||||
| chr4:26693310 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.954+4903A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693310 | |||||||
| chr4:26693393 | G | A | 1 | a0001c0010t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.954+4986G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693393 | |||||||
| chr4:26693411 | A | G | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+5004A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693411 | |||||||
| chr4:26693687 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+5280C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693687 | |||||||
| chr4:26693702 | A | T | 1 | a0001c0002t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.954+5295A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693702 | |||||||
| chr4:26693765 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.954+5358A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693765 | |||||||
| chr4:26693836 | C | T | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+5429C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693836 | |||||||
| chr4:26693983 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+5576T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693983 | |||||||
| chr4:26694036 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.954+5629G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694036 | |||||||
| chr4:26694074 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+5667G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694074 | |||||||
| chr4:26694075 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954+5668A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694075 | |||||||
| chr4:26694098 | G | T | 101 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.954+5691G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694098 | |||||||
| chr4:26694112 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+5705G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694112 | |||||||
| chr4:26694169 | G | A | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+5762G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694169 | |||||||
| chr4:26694254 | C | T | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+5847C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694254 | |||||||
| chr4:26694255 | A | G | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+5848A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694255 | |||||||
| chr4:26694482 | C | T | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+6075C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694482 | |||||||
| chr4:26694529 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.954+6122G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694529 | |||||||
| chr4:26694568 | G | C | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.954+6161G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694568 | |||||||
| chr4:26694671 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.954+6264G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694671 | |||||||
| chr4:26694759 | C | T | 5 | a0001c0001t0009g0175 a0001c0002t0002g0305 a0001c0002t0002g0306 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+6352C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694759 | |||||||
| chr4:26694760 | G | A | 19 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.954+6353G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694760 | |||||||
| chr4:26694776 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.954+6369C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694776 | |||||||
| chr4:26694954 | A | G | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+6547A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694954 | |||||||
| chr4:26695055 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+6648C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695055 | |||||||
| chr4:26695200 | C | T | 1 | a0001c0010t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.954+6793C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695200 | |||||||
| chr4:26695213 | C | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+6806C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695213 | |||||||
| chr4:26695293 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.954+6886G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695293 | |||||||
| chr4:26695643 | G | A | 1 | a0004c0009t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.954+7236G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695643 | |||||||
| chr4:26695671 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.954+7264T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695671 | |||||||
| chr4:26695798 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.954+7391A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695798 | |||||||
| chr4:26695883 | G | T | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+7476G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695883 | |||||||
| chr4:26695928 | T | C | 1 | a0001c0002t0002g0248 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.954+7521T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695928 | |||||||
| chr4:26695965 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.954+7558A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695965 | |||||||
| chr4:26696065 | C | T | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.954+7658C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696065 | |||||||
| chr4:26696182 | C | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+7775C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696182 | |||||||
| chr4:26696433 | A | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+8026A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696433 | |||||||
| chr4:26696449 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+8042C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696449 | |||||||
| chr4:26696512 | C | T | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+8105C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696512 | |||||||
| chr4:26696628 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.954+8221C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696628 | |||||||
| chr4:26696724 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.954+8317A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696724 | |||||||
| chr4:26696823 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.954+8416A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696823 | |||||||
| chr4:26696899 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.954+8492C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696899 | |||||||
| chr4:26696903 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+8496G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696903 | |||||||
| chr4:26696926 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.954+8519C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696926 | |||||||
| chr4:26696985 | A | C | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+8578A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696985 | |||||||
| chr4:26696990 | A | G | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+8583A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696990 | |||||||
| chr4:26697038 | A | G | 18 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+8631A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697038 | |||||||
| chr4:26697099 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+8692A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697099 | |||||||
| chr4:26697172 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+8765G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697172 | |||||||
| chr4:26697255 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.954+8848A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697255 | |||||||
| chr4:26697308 | C | G | 1 | a0001c0002t0002g0296 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.954+8901C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697308 | |||||||
| chr4:26697370 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.954+8963A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697370 | |||||||
| chr4:26697383 | C | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+8976C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697383 | |||||||
| chr4:26697577 | C | T | 2 | a0001c0002t0002g0283 a0001c0002t0002g0284 |
2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.954+9170C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697577 | |||||||
| chr4:26697620 | AC | A | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.954+9214delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697620 | |||||||
| chr4:26697782 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+9375G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697782 | |||||||
| chr4:26697811 | A | G | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+9404A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697811 | |||||||
| chr4:26697813 | A | C | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+9406A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697813 | |||||||
| chr4:26697908 | T | C | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+9501T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697908 | |||||||
| chr4:26698141 | G | A | 1 | a0001c0002t0002g0288 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.954+9734G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698141 | |||||||
| chr4:26698259 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0082 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.954+9852A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698259 | |||||||
| chr4:26698335 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.954+9928A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698335 | |||||||
| chr4:26698350 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.954+9943A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698350 | |||||||
| chr4:26698531 | C | A | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.954+10124C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698531 | |||||||
| chr4:26698561 | A | C | 32 | a0001c0002t0002g0154 a0001c0002t0002g0212 a0001c0002t0002g0272 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.954+10154A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698561 | |||||||
| chr4:26698817 | A | G | 1 | a0001c0002t0002g0265 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.954+10410A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698817 | |||||||
| chr4:26698840 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+10433T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698840 | |||||||
| chr4:26698897 | A | T | 18 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+10490A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698897 | |||||||
| chr4:26698924 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.954+10517A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698924 | |||||||
| chr4:26698943 | A | G | 2 | a0001c0001t0003g0193 a0001c0001t0003g0194 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.954+10536A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698943 | |||||||
| chr4:26699198 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+10791T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699198 | |||||||
| chr4:26699247 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.954+10840C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699247 | |||||||
| chr4:26699250 | G | A | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+10843G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699250 | |||||||
| chr4:26699281 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.954+10874A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699281 | |||||||
| chr4:26699317 | C | T | 1 | a0004c0009t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.954+10910C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699317 | |||||||
| chr4:26699321 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954+10914C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699321 | |||||||
| chr4:26699364 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.954+10957C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699364 | |||||||
| chr4:26699500 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+11093G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699500 | |||||||
| chr4:26699576 | C | T | 9 | a0001c0002t0002g0203 a0001c0002t0002g0213 a0001c0002t0002g0225 others(6): Show |
9 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+11169C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699576 | |||||||
| chr4:26699628 | T | G | 118 | a0001c0001t0001g0169 a0001c0001t0002g0019 a0001c0001t0002g0116 others(115): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.954+11221T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699628 | |||||||
| chr4:26699629 | G | A | 118 | a0001c0001t0001g0169 a0001c0001t0002g0019 a0001c0001t0002g0116 others(115): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.954+11222G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699629 | |||||||
| chr4:26699652 | G | A | 6 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0006t0001g0211 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+11245G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699652 | |||||||
| chr4:26699739 | C | T | 1 | a0001c0003t0001g0024 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.954+11332C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699739 | |||||||
| chr4:26699780 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.954+11373A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699780 | |||||||
| chr4:26699801 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.954+11394G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699801 | |||||||
| chr4:26699838 | G | C | 1 | a0001c0002t0002g0218 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.954+11431G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699838 | |||||||
| chr4:26699884 | G | A | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+11477G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699884 | |||||||
| chr4:26700106 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.954+11699G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700106 | |||||||
| chr4:26700134 | A | G | 1 | a0001c0005t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.954+11727A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700134 | |||||||
| chr4:26700314 | A | G | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+11907A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700314 | |||||||
| chr4:26700470 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+12063C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700470 | |||||||
| chr4:26700500 | G | A | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+12093G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700500 | |||||||
| chr4:26700518 | G | A | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.954+12111G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700518 | |||||||
| chr4:26700542 | C | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+12135C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700542 | |||||||
| chr4:26700600 | T | C | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+12193T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700600 | |||||||
| chr4:26700716 | A | T | 3 | a0001c0002t0002g0282 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.954+12309A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700716 | |||||||
| chr4:26700723 | A | G | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+12316A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700723 | |||||||
| chr4:26700904 | C | T | 4 | a0001c0002t0002g0226 a0001c0002t0002g0227 a0001c0002t0002g0254 others(1): Show |
4 | HG00140.hp2 HG01517.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+12497C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700904 | |||||||
| chr4:26701215 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.954+12808A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701215 | |||||||
| chr4:26701272 | C | G | 1 | a0001c0001t0008g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.954+12865C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701272 | |||||||
| chr4:26701314 | C | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.954+12907C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701314 | |||||||
| chr4:26701321 | AACAC | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+12920_954+1292 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26701321 | ||||||
| chr4:26701393 | TA | T | 7 | a0001c0001t0001g0191 a0001c0001t0008g0148 a0001c0001t0008g0209 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+12987delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701393 | |||||||
| chr4:26701563 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+13156A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701563 | |||||||
| chr4:26701571 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.954+13164G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701571 | |||||||
| chr4:26701622 | C | G | 1 | a0001c0005t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.954+13215C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701622 | |||||||
| chr4:26701744 | TA | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+13345delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26701744 | ||||||
| chr4:26701752 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+13345A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701752 | |||||||
| chr4:26702038 | C | G | 18 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+13631C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702038 | |||||||
| chr4:26702085 | T | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.954+13678T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702085 | |||||||
| chr4:26702241 | T | C | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.954+13834T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702241 | |||||||
| chr4:26702284 | C | A | 1 | a0001c0002t0002g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.954+13877C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702284 | |||||||
| chr4:26702417 | G | A | 1 | a0001c0002t0002g0292 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.954+14010G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702417 | |||||||
| chr4:26702538 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.954+14131A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702538 | |||||||
| chr4:26702878 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+14471G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702878 | |||||||
| chr4:26702908 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+14501A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702908 | |||||||
| chr4:26703411 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.955-14522T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703411 | |||||||
| chr4:26703494 | G | A | 1 | a0001c0005t0001g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.955-14439G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703494 | |||||||
| chr4:26703513 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.955-14420G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703513 | |||||||
| chr4:26703682 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.955-14251G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703682 | |||||||
| chr4:26703799 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.955-14134A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703799 | |||||||
| chr4:26703801 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0033 others(1): Show |
4 | HG00642.hp1 HG02683.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-14132A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703801 | |||||||
| chr4:26703821 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.955-14112C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703821 | |||||||
| chr4:26703829 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-14104C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703829 | |||||||
| chr4:26703857 | A | C | 9 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(6): Show |
9 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-14076A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703857 | |||||||
| chr4:26703955 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.955-13978C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703955 | |||||||
| chr4:26703960 | C | CA | 74 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0117 others(71): Show |
74 | HG00609.hp1 HG00733.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.955-13957dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26703960 | ||||||
| chr4:26703960 | C | CAA | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.955-13958_955-1395 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26703960 | ||||||
| chr4:26703960 | C | CAAA | 15 | a0001c0001t0001g0069 a0001c0001t0001g0155 a0001c0001t0003g0192 others(12): Show |
15 | HG00140.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.955-13959_955-1395 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26703960 | ||||||
| chr4:26704148 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-13785G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704148 | |||||||
| chr4:26704254 | T | C | 1 | a0001c0002t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.955-13679T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704254 | |||||||
| chr4:26704314 | G | GT | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.955-13618dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26704314 | ||||||
| chr4:26704344 | G | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.955-13589G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704344 | |||||||
| chr4:26704414 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0071 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.955-13519C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704414 | |||||||
| chr4:26704720 | A | C | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-13213A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704720 | |||||||
| chr4:26705011 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-12922A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705011 | |||||||
| chr4:26705030 | ATCT | A | 18 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-12901_955-1289 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26705030 | ||||||
| chr4:26705124 | TTTG | T | 100 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(97): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.955-12794_955-1279 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26705124 | ||||||
| chr4:26705125 | TTG | T | 9 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(6): Show |
9 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-12806_955-1280 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26705125 | ||||||
| chr4:26705127 | G | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.955-12806G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705127 | |||||||
| chr4:26705338 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955-12595G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705338 | |||||||
| chr4:26705378 | G | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955-12555G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705378 | |||||||
| chr4:26705436 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.955-12497C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705436 | |||||||
| chr4:26705606 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.955-12327G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705606 | |||||||
| chr4:26705790 | G | A | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.955-12143G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705790 | |||||||
| chr4:26705814 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.955-12119A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705814 | |||||||
| chr4:26706004 | C | A | 1 | a0001c0010t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.955-11929C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706004 | |||||||
| chr4:26706056 | T | C | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-11877T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706056 | |||||||
| chr4:26706281 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.955-11652G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706281 | |||||||
| chr4:26706305 | T | C | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955-11628T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706305 | |||||||
| chr4:26706308 | G | T | 1 | a0001c0002t0002g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.955-11625G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706308 | |||||||
| chr4:26706497 | T | A | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-11436T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706497 | |||||||
| chr4:26706537 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955-11396T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706537 | |||||||
| chr4:26706709 | C | T | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-11224C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706709 | |||||||
| chr4:26707177 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.955-10756T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707177 | |||||||
| chr4:26707234 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-10699A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707234 | |||||||
| chr4:26707279 | A | C | 1 | a0001c0002t0002g0242 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.955-10654A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707279 | |||||||
| chr4:26707343 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-10590G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707343 | |||||||
| chr4:26707491 | C | T | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.955-10442C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707491 | |||||||
| chr4:26707606 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.955-10327A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707606 | |||||||
| chr4:26707855 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-10078A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707855 | |||||||
| chr4:26707859 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-10074G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707859 | |||||||
| chr4:26707864 | T | C | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-10069T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707864 | |||||||
| chr4:26707921 | A | T | 3 | a0001c0002t0002g0282 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.955-10012A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707921 | |||||||
| chr4:26708016 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.955-9917A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708016 | |||||||
| chr4:26708082 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9851A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708082 | |||||||
| chr4:26708110 | A | G | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-9823A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708110 | |||||||
| chr4:26708177 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-9756G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708177 | |||||||
| chr4:26708223 | G | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-9710G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708223 | |||||||
| chr4:26708321 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9612A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708321 | |||||||
| chr4:26708397 | C | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.955-9536C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708397 | |||||||
| chr4:26708514 | C | A | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-9419C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708514 | |||||||
| chr4:26708523 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9410G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708523 | |||||||
| chr4:26708580 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.955-9353C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708580 | |||||||
| chr4:26708604 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.955-9329C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708604 | |||||||
| chr4:26708658 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0016 others(8): Show |
11 | HG00609.hp2 HG00673.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.955-9275A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708658 | |||||||
| chr4:26708666 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9267T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708666 | |||||||
| chr4:26708897 | G | GT | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-9030dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26708897 | ||||||
| chr4:26709113 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.955-8820T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709113 | |||||||
| chr4:26709114 | C | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.955-8819C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709114 | |||||||
| chr4:26709272 | A | G | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955-8661A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709272 | |||||||
| chr4:26709419 | G | C | 18 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0171 others(15): Show |
18 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.955-8514G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709419 | |||||||
| chr4:26709530 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.955-8403C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709530 | |||||||
| chr4:26709545 | G | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0090 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.955-8388G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709545 | |||||||
| chr4:26709648 | C | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.955-8285C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709648 | |||||||
| chr4:26709692 | A | T | 3 | a0001c0002t0002g0272 a0001c0002t0002g0292 a0001c0002t0002g0294 |
3 | HG01256.hp2 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.955-8241A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709692 | |||||||
| chr4:26709855 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.955-8078A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709855 | |||||||
| chr4:26709953 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.955-7980C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709953 | |||||||
| chr4:26710027 | G | GT | 9 | a0001c0001t0001g0069 a0001c0001t0003g0192 a0001c0001t0003g0193 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-7897dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26710027 | ||||||
| chr4:26710070 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.955-7863G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710070 | |||||||
| chr4:26710106 | G | A | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-7827G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710106 | |||||||
| chr4:26710221 | C | T | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-7712C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710221 | |||||||
| chr4:26710463 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.955-7470G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710463 | |||||||
| chr4:26710477 | T | C | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.955-7456T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710477 | |||||||
| chr4:26710494 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-7439G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710494 | |||||||
| chr4:26710548 | G | A | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.955-7385G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710548 | |||||||
| chr4:26710555 | G | A | 18 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-7378G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710555 | |||||||
| chr4:26710557 | T | C | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-7376T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710557 | |||||||
| chr4:26710689 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.955-7244C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710689 | |||||||
| chr4:26710747 | T | C | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-7186T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710747 | |||||||
| chr4:26710769 | T | A | 1 | a0001c0002t0002g0295 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.955-7164T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710769 | |||||||
| chr4:26710782 | A | C | 35 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(32): Show |
35 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.955-7151A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710782 | |||||||
| chr4:26710856 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0189 a0001c0002t0002g0236 others(1): Show |
4 | HG02970.hp2 NA18962.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-7077G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710856 | |||||||
| chr4:26710889 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-7044T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710889 | |||||||
| chr4:26710929 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.955-7004C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710929 | |||||||
| chr4:26710981 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0044 |
2 | NA18955.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.955-6952C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710981 | |||||||
| chr4:26711079 | C | T | 1 | a0001c0002t0002g0213 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.955-6854C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26711079 | |||||||
| chr4:26711663 | T | C | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-6270T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26711663 | |||||||
| chr4:26711900 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.955-6033C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26711900 | |||||||
| chr4:26712248 | G | C | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-5685G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26712248 | |||||||
| chr4:26712742 | A | C | 1 | a0001c0002t0002g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.955-5191A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26712742 | |||||||
| chr4:26713122 | A | C | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-4811A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713122 | |||||||
| chr4:26713137 | CA | C | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-4788delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26713137 | ||||||
| chr4:26713168 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.955-4765C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713168 | |||||||
| chr4:26713173 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-4760A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713173 | |||||||
| chr4:26713176 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955-4757A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713176 | |||||||
| chr4:26713196 | G | A | 1 | a0001c0004t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-4737G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713196 | |||||||
| chr4:26713420 | T | A | 1 | a0001c0002t0002g0297 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.955-4513T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713420 | |||||||
| chr4:26713421 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.955-4512G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713421 | |||||||
| chr4:26713542 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.955-4391A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713542 | |||||||
| chr4:26713787 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.955-4146G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713787 | |||||||
| chr4:26713907 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.955-4026G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713907 | |||||||
| chr4:26713975 | G | A | 18 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(15): Show |
18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-3958G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713975 | |||||||
| chr4:26714083 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.955-3850C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714083 | |||||||
| chr4:26714264 | C | CT | 27 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(24): Show |
27 | HG00140.hp2 HG00741.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.955-3660dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26714264 | ||||||
| chr4:26714298 | A | G | 9 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(6): Show |
9 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-3635A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714298 | |||||||
| chr4:26714338 | G | T | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.955-3595G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714338 | |||||||
| chr4:26714342 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.955-3591T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714342 | |||||||
| chr4:26714379 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.955-3554G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714379 | |||||||
| chr4:26714451 | A | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-3482A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714451 | |||||||
| chr4:26714589 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.955-3344C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714589 | |||||||
| chr4:26714841 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.955-3092A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714841 | |||||||
| chr4:26714850 | G | A | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-3083G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714850 | |||||||
| chr4:26714879 | G | A | 1 | a0001c0002t0002g0306 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.955-3054G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714879 | |||||||
| chr4:26715017 | A | G | 3 | a0001c0002t0002g0282 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.955-2916A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715017 | |||||||
| chr4:26715305 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.955-2628A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715305 | |||||||
| chr4:26715354 | A | G | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-2579A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715354 | |||||||
| chr4:26715439 | C | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-2494C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715439 | |||||||
| chr4:26715940 | C | T | 3 | a0001c0002t0002g0300 a0001c0002t0002g0301 a0001c0002t0002g0302 |
3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.955-1993C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715940 | |||||||
| chr4:26716055 | C | T | 3 | a0001c0002t0002g0226 a0001c0002t0002g0254 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG01517.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.955-1878C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716055 | |||||||
| chr4:26716290 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.955-1643C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716290 | |||||||
| chr4:26716339 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.955-1594A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716339 | |||||||
| chr4:26716872 | C | G | 1 | a0001c0002t0002g0242 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.955-1061C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716872 | |||||||
| chr4:26716936 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.955-997A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716936 | |||||||
| chr4:26717055 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.955-878C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717055 | |||||||
| chr4:26717273 | C | A | 1 | a0001c0002t0002g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.955-660C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717273 | |||||||
| chr4:26717764 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.955-169A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717764 | |||||||
| chr4:26717802 | G | A | 1 | a0001c0002t0002g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.955-131G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717802 | |||||||
| chr4:26717847 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-86A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717847 | |||||||
| chr4:26718129 | A | G | 1 | a0001c0002t0002g0265 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1039+112A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718129 | |||||||
| chr4:26718199 | C | G | 1 | a0001c0002t0002g0221 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1039+182C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718199 | |||||||
| chr4:26718200 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1039+183G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718200 | |||||||
| chr4:26718311 | C | CTAACTA | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1039+297_1039+298i others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr4 | 26718311 | ||||||
| chr4:26718342 | C | CT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1039+332dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr4 | 26718342 | ||||||
| chr4:26718354 | A | C | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1039+337A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718354 | |||||||
| chr4:26718505 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1039+488A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718505 | |||||||
| chr4:26718601 | C | T | 1 | a0001c0002t0002g0281 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1039+584C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718601 | |||||||
| chr4:26718634 | G | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1039+617G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718634 | |||||||
| chr4:26718940 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1039+923C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718940 | |||||||
| chr4:26719003 | T | C | 9 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039+986T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719003 | |||||||
| chr4:26719149 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1040-932A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719149 | |||||||
| chr4:26719191 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1040-890C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719191 | |||||||
| chr4:26719221 | T | G | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-860T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719221 | |||||||
| chr4:26719520 | G | T | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1040-561G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719520 | |||||||
| chr4:26719619 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1040-462A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719619 | |||||||
| chr4:26719672 | A | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040-409A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719672 | |||||||
| chr4:26719695 | C | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1040-386C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719695 | |||||||
| chr4:26719724 | C | G | 2 | a0001c0001t0007g0029 a0001c0001t0007g0030 |
2 | HG02083.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1040-357C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719724 | |||||||
| chr4:26719880 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-201G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719880 | |||||||
| chr4:26719916 | A | G | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1040-165A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719916 | |||||||
| chr4:26719956 | T | C | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1040-125T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719956 | |||||||
| chr4:26720190 | T | C | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+65T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720190 | |||||||
| chr4:26720197 | TTC | T | 14 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(11): Show |
14 | HG00741.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084+74_1084+75del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26720197 | ||||||
| chr4:26720285 | G | T | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+160G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720285 | |||||||
| chr4:26720341 | A | G | 1 | a0001c0002t0002g0248 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1084+216A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720341 | |||||||
| chr4:26720414 | A | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+289A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720414 | |||||||
| chr4:26720526 | GA | G | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+404delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26720526 | ||||||
| chr4:26720800 | A | G | 1 | a0001c0002t0002g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1084+675A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720800 | |||||||
| chr4:26721268 | A | G | 2 | a0001c0002t0002g0260 a0001c0002t0002g0261 |
2 | HG00544.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1084+1143A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721268 | |||||||
| chr4:26721341 | A | G | 1 | a0001c0003t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1084+1216A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721341 | |||||||
| chr4:26721553 | T | G | 1 | a0001c0002t0002g0287 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1084+1428T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721553 | |||||||
| chr4:26721614 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+1489C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721614 | |||||||
| chr4:26721649 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1084+1524T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721649 | |||||||
| chr4:26721678 | C | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(17): Show |
20 | HG00621.hp2 HG01993.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1084+1553C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721678 | |||||||
| chr4:26721686 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1084+1561C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721686 | |||||||
| chr4:26721803 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+1678C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721803 | |||||||
| chr4:26722146 | A | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0057 |
2 | HG01934.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1084+2021A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722146 | |||||||
| chr4:26722219 | C | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0185 others(1): Show |
4 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+2094C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722219 | |||||||
| chr4:26722536 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1084+2411A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722536 | |||||||
| chr4:26722569 | A | C | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+2444A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722569 | |||||||
| chr4:26722693 | A | C | 1 | a0001c0004t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1084+2568A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722693 | |||||||
| chr4:26722711 | G | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1084+2586G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722711 | |||||||
| chr4:26723074 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1084+2949A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723074 | |||||||
| chr4:26723230 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1084+3105A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723230 | |||||||
| chr4:26723416 | G | A | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | NA18957.hp1 NA18964.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084+3291G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723416 | |||||||
| chr4:26723701 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1084+3576T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723701 | |||||||
| chr4:26723732 | A | G | 1 | a0001c0002t0002g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1084+3607A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723732 | |||||||
| chr4:26723754 | A | C | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1084+3629A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723754 | |||||||
| chr4:26724018 | G | A | 1 | a0003c0008t0006g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1084+3893G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724018 | |||||||
| chr4:26724054 | A | T | 7 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(4): Show |
7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084+3929A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724054 | |||||||
| chr4:26724059 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1084+3934A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724059 | |||||||
| chr4:26724305 | G | T | 8 | a0001c0002t0002g0203 a0001c0002t0002g0213 a0001c0002t0002g0262 others(5): Show |
8 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084+4180G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724305 | |||||||
| chr4:26724478 | CT | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0001g0096 others(1): Show |
4 | HG00621.hp2 NA18964.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+4357delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26724478 | ||||||
| chr4:26724637 | C | G | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1084+4512C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724637 | |||||||
| chr4:26724638 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1084+4513T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724638 | |||||||
| chr4:26724675 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1084+4550C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724675 | |||||||
| chr4:26724793 | ATTCCCCT others(15): Show |
A | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+4673_1084+469 others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26724793 | ||||||
| chr4:26724805 | A | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG02559.hp2 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+4680A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724805 | |||||||
| chr4:26724878 | T | C | 1 | a0001c0003t0001g0043 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1084+4753T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724878 | |||||||
| chr4:26725158 | C | T | 122 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(119): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1084+5033C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725158 | |||||||
| chr4:26725205 | T | C | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+5080T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725205 | |||||||
| chr4:26725347 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1084+5222G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725347 | |||||||
| chr4:26725475 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+5350G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725475 | |||||||
| chr4:26725497 | G | A | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084+5372G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725497 | |||||||
| chr4:26726056 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(8): Show |
11 | NA18941.hp1 NA18946.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084+5931G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726056 | |||||||
| chr4:26726095 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1084+5970G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726095 | |||||||
| chr4:26726122 | TCCCAACA others(4): Show |
T | 1 | a0001c0002t0002g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1084+5999_1084+600 others(15): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726122 | ||||||
| chr4:26726122 | TCCCAACA others(7): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1084+5998_1084+601 others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726122 | |||||||
| chr4:26726126 | A | AAC | 3 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG00733.hp1 HG03041.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1084+6053_1084+605 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AAC | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0045 others(20): Show |
23 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1084+6053_1084+605 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACAC | A | 67 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0020 others(64): Show |
67 | HG00280.hp1 HG00323.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1084+6051_1084+605 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACACAC | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1084+6049_1084+605 others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACACACA others(1): Show |
A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0021 others(46): Show |
49 | HG00609.hp1 HG01243.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.1084+6047_1084+605 others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACACACA others(3): Show |
A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0077 others(10): Show |
13 | HG02257.hp2 HG02683.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.1084+6045_1084+605 others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACACACA others(5): Show |
A | 22 | a0001c0001t0001g0005 a0001c0002t0002g0154 a0001c0002t0002g0272 others(19): Show |
22 | HG00639.hp2 HG01256.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1084+6043_1084+605 others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACACACA others(9): Show |
A | 6 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG00323.hp2 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084+6039_1084+605 others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726126 | AACACACA others(13): Show |
A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0169 others(1): Show |
4 | HG00738.hp1 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+6035_1084+605 others(24): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | ||||||
| chr4:26726236 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1084+6111G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726236 | |||||||
| chr4:26726404 | C | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1084+6279C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726404 | |||||||
| chr4:26726538 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+6413C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726538 | |||||||
| chr4:26726651 | T | TACATATG others(5): Show |
1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1084+6528_1084+653 others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726651 | ||||||
| chr4:26726673 | A | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG02559.hp2 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+6548A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726673 | |||||||
| chr4:26726690 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1084+6565C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726690 | |||||||
| chr4:26726759 | CAGAT | C | 4 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+6637_1084+664 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726759 | ||||||
| chr4:26726774 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0185 others(1): Show |
4 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+6649C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726774 | |||||||
| chr4:26726825 | G | GAA | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1084+6701_1084+670 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726825 | ||||||
| chr4:26726848 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+6723T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726848 | |||||||
| chr4:26727016 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1084+6891A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727016 | |||||||
| chr4:26727033 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1084+6908A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727033 | |||||||
| chr4:26727097 | C | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1084+6972C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727097 | |||||||
| chr4:26727119 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1084+6994C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727119 | |||||||
| chr4:26727124 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+6999C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727124 | |||||||
| chr4:26727233 | A | G | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1084+7108A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727233 | |||||||
| chr4:26727320 | A | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1084+7195A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727320 | |||||||
| chr4:26727510 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1084+7385G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727510 | |||||||
| chr4:26727526 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1084+7401A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727526 | |||||||
| chr4:26727952 | CTACT | C | 20 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(17): Show |
20 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1085-7500_1085-749 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26727952 | ||||||
| chr4:26728189 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1085-7266C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728189 | |||||||
| chr4:26728373 | C | T | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1085-7082C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728373 | |||||||
| chr4:26728531 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0191 |
2 | HG00140.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1085-6924G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728531 | |||||||
| chr4:26728560 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-6895T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728560 | |||||||
| chr4:26728580 | A | G | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1085-6875A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728580 | |||||||
| chr4:26728591 | G | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-6864G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728591 | |||||||
| chr4:26728663 | A | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-6792A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728663 | |||||||
| chr4:26728836 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-6619A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728836 | |||||||
| chr4:26729595 | G | T | 1 | a0001c0002t0002g0291 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1085-5860G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729595 | |||||||
| chr4:26729663 | A | G | 1 | a0001c0003t0001g0011 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1085-5792A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729663 | |||||||
| chr4:26729668 | G | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1085-5787G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729668 | |||||||
| chr4:26729699 | G | A | 1 | a0001c0002t0002g0219 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1085-5756G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729699 | |||||||
| chr4:26729877 | T | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1085-5578T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729877 | |||||||
| chr4:26730006 | T | G | 1 | a0001c0002t0002g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1085-5449T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730006 | |||||||
| chr4:26730032 | T | C | 20 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1085-5423T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730032 | |||||||
| chr4:26730203 | T | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-5252T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730203 | |||||||
| chr4:26730405 | G | A | 1 | a0001c0002t0010g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1085-5050G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730405 | |||||||
| chr4:26730484 | C | T | 1 | a0001c0002t0002g0299 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1085-4971C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730484 | |||||||
| chr4:26730824 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-4631T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730824 | |||||||
| chr4:26730959 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1085-4496A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730959 | |||||||
| chr4:26730998 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1085-4457A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730998 | |||||||
| chr4:26731142 | G | A | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-4313G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731142 | |||||||
| chr4:26731171 | G | A | 1 | a0001c0003t0001g0011 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1085-4284G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731171 | |||||||
| chr4:26731189 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-4266G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731189 | |||||||
| chr4:26731200 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1085-4255A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731200 | |||||||
| chr4:26731235 | G | C | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-4220G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731235 | |||||||
| chr4:26731487 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1085-3968A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731487 | |||||||
| chr4:26731631 | A | T | 9 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(6): Show |
9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-3824A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731631 | |||||||
| chr4:26731663 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-3792C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731663 | |||||||
| chr4:26731683 | GAAACA | G | 4 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 others(1): Show |
4 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-3764_1085-376 others(9): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26731683 | ||||||
| chr4:26731767 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1085-3688C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731767 | |||||||
| chr4:26731852 | G | A | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1085-3603G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731852 | |||||||
| chr4:26731856 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-3599G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731856 | |||||||
| chr4:26731944 | G | A | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-3511G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731944 | |||||||
| chr4:26731961 | G | A | 1 | a0001c0006t0005g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1085-3494G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731961 | |||||||
| chr4:26732103 | G | A | 5 | a0001c0001t0009g0175 a0001c0002t0002g0226 a0001c0002t0002g0227 others(2): Show |
5 | HG00140.hp2 HG01517.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-3352G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732103 | |||||||
| chr4:26732150 | A | T | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-3305A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732150 | |||||||
| chr4:26732173 | T | G | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1085-3282T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732173 | |||||||
| chr4:26732294 | C | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1085-3161C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732294 | |||||||
| chr4:26732358 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0204 |
3 | HG00738.hp1 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1085-3097T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732358 | |||||||
| chr4:26732548 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-2907G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732548 | |||||||
| chr4:26733041 | A | G | 19 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1085-2414A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733041 | |||||||
| chr4:26733176 | C | T | 10 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(7): Show |
10 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1085-2279C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733176 | |||||||
| chr4:26733200 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1085-2255T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733200 | |||||||
| chr4:26733353 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1085-2102G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733353 | |||||||
| chr4:26733454 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0054 others(2): Show |
5 | NA18941.hp1 NA18960.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-2001T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733454 | |||||||
| chr4:26733460 | G | GACAC | 3 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0010t0001g0034 |
3 | HG02615.hp2 NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1085-1974_1085-197 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26733460 | ||||||
| chr4:26733460 | GAC | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1085-1972_1085-197 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26733460 | ||||||
| chr4:26733640 | A | G | 10 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1085-1815A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733640 | |||||||
| chr4:26733678 | T | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1085-1777T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733678 | |||||||
| chr4:26733978 | T | A | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1085-1477T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733978 | |||||||
| chr4:26733990 | C | A | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1085-1465C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733990 | |||||||
| chr4:26734069 | T | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-1386T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734069 | |||||||
| chr4:26734566 | G | A | 20 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(17): Show |
20 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1085-889G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734566 | |||||||
| chr4:26734851 | G | A | 1 | a0001c0003t0001g0043 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1085-604G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734851 | |||||||
| chr4:26734890 | ATG | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1085-557_1085-556d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734890 | ||||||
| chr4:26734925 | CAT | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(20): Show |
23 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(20): Show |
intron_variant | MODIFIER | c.1085-525_1085-524d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734925 | ||||||
| chr4:26734930 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-525A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734930 | |||||||
| chr4:26734932 | GTGTGTAT others(21): Show |
G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-519_1085-492d others(30): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734932 | ||||||
| chr4:26734934 | G | GTGTATAT others(19): Show |
103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1085-465_1085-440d others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734934 | ||||||
| chr4:26734934 | G | GTGTATAT others(45): Show |
4 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0167 others(1): Show |
4 | HG01261.hp2 HG01981.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-491_1085-440d others(54): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734934 | ||||||
| chr4:26734934 | GTGTATAT others(19): Show |
G | 109 | a0001c0001t0001g0050 a0001c0001t0002g0019 a0001c0001t0002g0116 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1085-465_1085-440d others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734934 | ||||||
| chr4:26734944 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-511G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734944 | |||||||
| chr4:26734977 | CAT | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(2): Show |
5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-475_1085-474d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734977 | ||||||
| chr4:26734985 | T | TATGTATA others(57): Show |
1 | a0001c0001t0007g0029 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1085-440_1085-439i others(66): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734985 | ||||||
| chr4:26734986 | A | G | 1 | a0001c0002t0002g0292 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1085-469A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734986 | |||||||
| chr4:26734990 | A | G | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-465A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734990 | |||||||
| chr4:26734994 | A | ATGTATAC others(19): Show |
1 | a0001c0001t0003g0199 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1085-440_1085-439i others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734994 | ||||||
| chr4:26734995 | T | C | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-460T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734995 | |||||||
| chr4:26734996 | G | A | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-459G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734996 | |||||||
| chr4:26734997 | T | C | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-458T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734997 | |||||||
| chr4:26735000 | A | G | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-455A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735000 | |||||||
| chr4:26735001 | C | T | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-454C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735001 | |||||||
| chr4:26735003 | C | CATATGTA others(41): Show |
1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1085-440_1085-439i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735003 | ||||||
| chr4:26735003 | C | CATATGTA others(45): Show |
1 | a0001c0001t0001g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1085-440_1085-439i others(54): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735003 | ||||||
| chr4:26735003 | C | CATATGTA others(19): Show |
4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-436_1085-411d others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735003 | ||||||
| chr4:26735003 | C | T | 1 | a0001c0002t0002g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-452C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735003 | |||||||
| chr4:26735005 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-450T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735005 | |||||||
| chr4:26735005 | T | TATGTATA others(19): Show |
1 | a0001c0001t0001g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1085-440_1085-439i others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735005 | ||||||
| chr4:26735019 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0009g0175 |
2 | HG01257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1085-436T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735019 | |||||||
| chr4:26735031 | T | C | 2 | a0001c0002t0002g0203 a0001c0002t0002g0262 |
2 | HG02071.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1085-424T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735031 | |||||||
| chr4:26735045 | C | CACACATG others(37): Show |
1 | a0001c0001t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1085-375_1085-332d others(46): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735045 | ||||||
| chr4:26735057 | T | TATGTATA others(11): Show |
4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-364_1085-347d others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735057 | ||||||
| chr4:26735057 | TATGTATA others(11): Show |
T | 1 | a0001c0002t0002g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1085-364_1085-347d others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735057 | ||||||
| chr4:26735066 | A | G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0169 a0001c0001t0001g0181 others(3): Show |
6 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1085-389A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735066 | |||||||
| chr4:26735108 | A | ACACATGT others(11): Show |
1 | a0001c0001t0001g0159 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1085-347_1085-346i others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735108 | |||||||
| chr4:26735108 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1085-347A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735108 | |||||||
| chr4:26735109 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1085-346T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735109 | |||||||
| chr4:26735120 | ATG | A | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085-327_1085-326d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735120 | ||||||
| chr4:26735166 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0085 others(1): Show |
4 | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-289A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735166 | |||||||
| chr4:26735184 | G | A | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1085-271G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735184 | |||||||
| chr4:26735236 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-219A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735236 | |||||||
| chr4:26735343 | G | C | 1 | a0001c0002t0002g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1085-112G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735343 | |||||||
| chr4:26735387 | C | A | 1 | a0001c0002t0002g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1085-68C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735387 | |||||||
| chr4:26735441 | C | CT | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1085-3dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735441 | ||||||
| chr4:26735592 | A | G | 1 | a0001c0002t0002g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1117+105A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735592 | |||||||
| chr4:26735635 | T | C | 1 | a0001c0003t0001g0026 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1117+148T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735635 | |||||||
| chr4:26735746 | G | C | 1 | a0001c0002t0002g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1117+259G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735746 | |||||||
| chr4:26735767 | G | A | 5 | a0001c0001t0001g0191 a0001c0006t0001g0211 a0001c0006t0005g0147 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117+280G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735767 | |||||||
| chr4:26735858 | A | G | 1 | a0001c0002t0002g0292 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1117+371A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735858 | |||||||
| chr4:26735923 | T | C | 8 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1117+436T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735923 | |||||||
| chr4:26735961 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1117+474G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735961 | |||||||
| chr4:26736005 | A | G | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+518A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736005 | |||||||
| chr4:26736096 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1117+609T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736096 | |||||||
| chr4:26736109 | T | C | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1117+622T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736109 | |||||||
| chr4:26736146 | C | CAA | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1117+660_1117+661i others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 26736146 | ||||||
| chr4:26736171 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1117+684T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736171 | |||||||
| chr4:26736222 | T | G | 1 | a0003c0008t0006g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1117+735T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736222 | |||||||
| chr4:26736311 | G | A | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1117+824G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736311 | |||||||
| chr4:26736349 | T | A | 2 | a0001c0002t0002g0241 a0001c0002t0002g0256 |
2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1117+862T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736349 | |||||||
| chr4:26736408 | G | T | 1 | a0004c0009t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1117+921G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736408 | |||||||
| chr4:26736491 | G | A | 128 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(125): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1117+1004G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736491 | |||||||
| chr4:26736577 | G | C | 20 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(17): Show |
20 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1117+1090G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736577 | |||||||
| chr4:26736879 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0071 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1117+1392T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736879 | |||||||
| chr4:26737068 | A | C | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1117+1581A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737068 | |||||||
| chr4:26737155 | C | T | 1 | a0001c0002t0002g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1117+1668C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737155 | |||||||
| chr4:26737502 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0050 others(3): Show |
6 | HG01257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1117+2015A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737502 | |||||||
| chr4:26737551 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1117+2064A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737551 | |||||||
| chr4:26737766 | A | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1118-2098A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737766 | |||||||
| chr4:26737866 | CA | C | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 |
3 | HG01884.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1118-1994delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 26737866 | ||||||
| chr4:26738142 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1118-1722C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738142 | |||||||
| chr4:26738220 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1118-1644A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738220 | |||||||
| chr4:26738234 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1118-1630C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738234 | |||||||
| chr4:26738740 | T | C | 1 | a0001c0004t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1118-1124T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738740 | |||||||
| chr4:26738909 | A | G | 2 | a0001c0002t0002g0241 a0001c0002t0002g0256 |
2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1118-955A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738909 | |||||||
| chr4:26739034 | G | A | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1118-830G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739034 | |||||||
| chr4:26739100 | A | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1118-764A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739100 | |||||||
| chr4:26739124 | A | C | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1118-740A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739124 | |||||||
| chr4:26739197 | G | A | 1 | a0001c0003t0001g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1118-667G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739197 | |||||||
| chr4:26739379 | G | T | 1 | a0001c0002t0002g0292 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1118-485G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739379 | |||||||
| chr4:26739461 | G | A | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0194 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118-403G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739461 | |||||||
| chr4:26739498 | C | T | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1118-366C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739498 | |||||||
| chr4:26739619 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1118-245G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739619 | |||||||
| chr4:26739730 | A | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1118-134A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739730 | |||||||
| chr4:26740215 | A | T | 2 | a0001c0001t0002g0019 a0001c0002t0002g0267 |
2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1227+242A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740215 | |||||||
| chr4:26740224 | A | T | 4 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 others(1): Show |
4 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+251A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740224 | |||||||
| chr4:26740327 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1227+354A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740327 | |||||||
| chr4:26740363 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+390G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740363 | |||||||
| chr4:26740779 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG02559.hp2 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+806C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740779 | |||||||
| chr4:26740833 | C | A | 1 | a0001c0002t0002g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1227+860C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740833 | |||||||
| chr4:26740983 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+1010A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740983 | |||||||
| chr4:26741130 | G | A | 1 | a0001c0001t0007g0030 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1227+1157G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741130 | |||||||
| chr4:26741280 | C | T | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228-1228C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741280 | |||||||
| chr4:26741310 | T | A | 4 | a0002c0007t0001g0163 a0002c0007t0001g0164 a0002c0007t0001g0165 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-1198T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741310 | |||||||
| chr4:26741349 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1228-1159C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741349 | |||||||
| chr4:26741362 | C | CA | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0048 others(7): Show |
10 | HG00738.hp2 HG01109.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1228-1122dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | ||||||
| chr4:26741362 | CA | C | 33 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0086 others(30): Show |
33 | HG00544.hp1 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1228-1122delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | ||||||
| chr4:26741362 | CAA | C | 111 | a0001c0001t0001g0149 a0001c0001t0001g0160 a0001c0001t0001g0161 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1228-1123_1228-112 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | ||||||
| chr4:26741362 | CAAA | C | 9 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG00741.hp1 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1228-1124_1228-112 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | ||||||
| chr4:26741383 | AAAAG | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(25): Show |
28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228-1123_1228-112 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741383 | ||||||
| chr4:26741628 | C | CT | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(27): Show |
30 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(27): Show |
intron_variant | MODIFIER | c.1228-866dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741628 | ||||||
| chr4:26741628 | CT | C | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0002g0305 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1228-866delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741628 | ||||||
| chr4:26741719 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1228-789A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741719 | |||||||
| chr4:26741785 | G | C | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1228-723G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741785 | |||||||
| chr4:26741838 | C | G | 1 | a0001c0001t0008g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1228-670C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741838 | |||||||
| chr4:26741900 | T | C | 1 | a0001c0002t0002g0235 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1228-608T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741900 | |||||||
| chr4:26742005 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1228-503G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26742005 | |||||||
| chr4:26742154 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0204 |
3 | HG00738.hp1 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1228-354A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26742154 | |||||||
| chr4:26742772 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1319+173C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26742772 | |||||||
| chr4:26743181 | T | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1319+582T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743181 | |||||||
| chr4:26743209 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1319+610G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743209 | |||||||
| chr4:26743239 | G | A | 1 | a0001c0002t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1319+640G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743239 | |||||||
| chr4:26743303 | A | G | 5 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1319+704A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743303 | |||||||
| chr4:26743564 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1319+965A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743564 | |||||||
| chr4:26743594 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1319+995G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743594 | |||||||
| chr4:26743783 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1319+1184C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743783 | |||||||
| chr4:26743970 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1319+1371A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743970 | |||||||
| chr4:26744321 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1319+1722A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744321 | |||||||
| chr4:26744328 | T | A | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1319+1729T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744328 | |||||||
| chr4:26744388 | T | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG00280.hp1 HG00738.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1319+1789T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744388 | |||||||
| chr4:26744841 | T | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(21): Show |
24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.1319+2242T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744841 | |||||||
| chr4:26744853 | T | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1319+2254T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744853 | |||||||
| chr4:26745119 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1319+2520A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745119 | |||||||
| chr4:26745208 | A | G | 28 | a0001c0001t0001g0086 a0001c0001t0001g0146 a0001c0001t0001g0149 others(25): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1319+2609A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745208 | |||||||
| chr4:26745326 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1319+2727C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745326 | |||||||
| chr4:26745331 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1319+2732A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745331 | |||||||
| chr4:26745452 | T | C | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1319+2853T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745452 | |||||||
| chr4:26745459 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0082 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1319+2860A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745459 | |||||||
| chr4:26745497 | C | CT | 101 | a0001c0001t0001g0146 a0001c0001t0001g0188 a0001c0001t0001g0189 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1320-2886dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | ||||||
| chr4:26745497 | C | CTT | 22 | a0001c0001t0001g0134 a0001c0001t0001g0149 a0001c0001t0001g0157 others(19): Show |
22 | HG00673.hp1 HG00741.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1320-2887_1320-288 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | ||||||
| chr4:26745497 | C | CTTT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0118 others(19): Show |
22 | HG00609.hp1 HG02886.hp1 HG03453.hp2 others(19): Show |
intron_variant | MODIFIER | c.1320-2888_1320-288 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | ||||||
| chr4:26745497 | CT | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1320-2886delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | ||||||
| chr4:26745665 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1320-2746C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745665 | |||||||
| chr4:26745700 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1320-2711C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745700 | |||||||
| chr4:26745718 | G | A | 1 | a0001c0002t0002g0297 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1320-2693G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745718 | |||||||
| chr4:26745731 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1320-2680C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745731 | |||||||
| chr4:26745878 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1320-2533C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745878 | |||||||
| chr4:26745888 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1320-2523C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745888 | |||||||
| chr4:26746196 | A | G | 30 | a0001c0002t0002g0154 a0001c0002t0002g0212 a0001c0002t0002g0223 others(27): Show |
30 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1320-2215A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746196 | |||||||
| chr4:26746228 | G | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1320-2183G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746228 | |||||||
| chr4:26746232 | AT | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
130 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1320-2161delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26746232 | ||||||
| chr4:26746232 | ATT | A | 8 | a0001c0001t0008g0148 a0001c0002t0002g0226 a0001c0002t0002g0227 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1320-2162_1320-216 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26746232 | ||||||
| chr4:26746332 | G | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1320-2079G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746332 | |||||||
| chr4:26746436 | A | G | 10 | a0001c0001t0001g0086 a0001c0001t0001g0171 a0001c0001t0001g0172 others(7): Show |
10 | HG00733.hp1 HG02630.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320-1975A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746436 | |||||||
| chr4:26746493 | A | ATG | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(43): Show |
46 | HG00609.hp1 HG00741.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1320-1916_1320-191 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26746493 | ||||||
| chr4:26746558 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1320-1853A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746558 | |||||||
| chr4:26746908 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1320-1503A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746908 | |||||||
| chr4:26747235 | A | G | 2 | a0001c0001t0008g0148 a0001c0001t0008g0209 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1320-1176A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747235 | |||||||
| chr4:26747508 | C | A | 1 | a0001c0003t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1320-903C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747508 | |||||||
| chr4:26747718 | T | C | 1 | a0001c0002t0002g0154 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1320-693T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747718 | |||||||
| chr4:26747746 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1320-665C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747746 | |||||||
| chr4:26747908 | A | G | 1 | a0001c0001t0004g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1320-503A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747908 | |||||||
| chr4:26748243 | T | C | 2 | a0001c0002t0002g0289 a0001c0002t0002g0290 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1320-168T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26748243 | |||||||
| chr4:26748599 | C | T | 1 | a0001c0006t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1435+73C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26748599 | |||||||
| chr4:26748870 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435+344T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26748870 | |||||||
| chr4:26748892 | C | T | 107 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1435+366C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26748892 | |||||||
| chr4:26749088 | T | G | 1 | a0001c0002t0010g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1435+562T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749088 | |||||||
| chr4:26749154 | C | G | 1 | a0001c0002t0002g0225 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1435+628C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749154 | |||||||
| chr4:26749216 | C | A | 1 | a0001c0002t0002g0281 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1435+690C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749216 | |||||||
| chr4:26749263 | A | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1435+737A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749263 | |||||||
| chr4:26749448 | GT | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
106 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1435+940delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26749448 | ||||||
| chr4:26749449 | T | TG | 100 | a0001c0001t0002g0116 a0001c0001t0002g0152 a0001c0001t0002g0153 others(97): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1435+923_1435+924i others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749449 | |||||||
| chr4:26749450 | T | G | 9 | a0001c0001t0008g0148 a0001c0001t0008g0209 a0001c0002t0002g0305 others(6): Show |
9 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1435+924T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749450 | |||||||
| chr4:26749635 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0046 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1435+1109C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749635 | |||||||
| chr4:26749889 | T | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1435+1363T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749889 | |||||||
| chr4:26750108 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1435+1582A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750108 | |||||||
| chr4:26750259 | T | G | 4 | a0001c0006t0001g0211 a0001c0006t0005g0147 a0001c0006t0005g0207 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+1733T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750259 | |||||||
| chr4:26750423 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1435+1897T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750423 | |||||||
| chr4:26750501 | C | A | 1 | a0001c0002t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1435+1975C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750501 | |||||||
| chr4:26750534 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435+2008C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750534 | |||||||
| chr4:26750587 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1435+2061G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750587 | |||||||
| chr4:26750633 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1435+2107G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750633 | |||||||
| chr4:26750753 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1435+2227G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750753 | |||||||
| chr4:26750823 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1435+2297T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750823 | |||||||
| chr4:26750883 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1435+2357C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750883 | |||||||
| chr4:26750974 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1435+2448A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750974 | |||||||
| chr4:26751061 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1435+2535A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751061 | |||||||
| chr4:26751093 | A | G | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1435+2567A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751093 | |||||||
| chr4:26751381 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0004g0022 |
3 | NA18955.hp1 NA19009.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1436-2439A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751381 | |||||||
| chr4:26751440 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1436-2380T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751440 | |||||||
| chr4:26751586 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1436-2234T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751586 | |||||||
| chr4:26751601 | T | C | 28 | a0001c0001t0001g0086 a0001c0001t0001g0146 a0001c0001t0001g0149 others(25): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1436-2219T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751601 | |||||||
| chr4:26751704 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1436-2116G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751704 | |||||||
| chr4:26751925 | T | A | 2 | a0001c0005t0001g0106 a0001c0005t0001g0190 |
2 | HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1436-1895T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751925 | |||||||
| chr4:26751951 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1436-1869C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751951 | |||||||
| chr4:26752019 | G | A | 17 | a0001c0001t0001g0086 a0001c0001t0001g0171 a0001c0001t0001g0172 others(14): Show |
17 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1436-1801G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752019 | |||||||
| chr4:26752136 | A | G | 102 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1436-1684A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752136 | |||||||
| chr4:26752204 | C | T | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1436-1616C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752204 | |||||||
| chr4:26752243 | C | CT | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
32 | HG00609.hp1 HG02559.hp2 HG03139.hp2 others(29): Show |
intron_variant | MODIFIER | c.1436-1558dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26752243 | ||||||
| chr4:26752243 | CT | C | 32 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0097 others(29): Show |
32 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1436-1558delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26752243 | ||||||
| chr4:26752243 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0015 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1436-1571_1436-155 others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26752243 | ||||||
| chr4:26752358 | G | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1436-1462G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752358 | |||||||
| chr4:26752491 | C | G | 9 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1436-1329C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752491 | |||||||
| chr4:26752573 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1436-1247C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752573 | |||||||
| chr4:26752623 | T | C | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1436-1197T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752623 | |||||||
| chr4:26752645 | A | T | 2 | a0001c0001t0003g0193 a0001c0001t0003g0194 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1436-1175A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752645 | |||||||
| chr4:26752797 | A | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(29): Show |
32 | HG00609.hp1 HG01243.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1436-1023A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752797 | |||||||
| chr4:26753013 | T | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0117 others(29): Show |
32 | HG00609.hp1 HG01243.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1436-807T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753013 | |||||||
| chr4:26753072 | T | C | 1 | a0001c0005t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1436-748T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753072 | |||||||
| chr4:26753264 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1436-556T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753264 | |||||||
| chr4:26753265 | G | A | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1436-555G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753265 | |||||||
| chr4:26753294 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1436-526A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753294 | |||||||
| chr4:26753535 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1436-285T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753535 | |||||||
| chr4:26753584 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0204 |
3 | HG00738.hp1 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1436-236A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753584 | |||||||
| chr4:26753651 | G | T | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1436-169G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753651 | |||||||
| chr4:26753715 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1436-105A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753715 | |||||||
| chr4:26754074 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1506+184A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754074 | |||||||
| chr4:26754169 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1506+279T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754169 | |||||||
| chr4:26754171 | G | A | 2 | a0003c0008t0006g0114 a0003c0008t0006g0115 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1506+281G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754171 | |||||||
| chr4:26754480 | A | G | 109 | a0001c0001t0002g0019 a0001c0001t0002g0116 a0001c0001t0002g0152 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1507-393A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754480 | |||||||
| chr4:26754504 | T | C | 3 | a0001c0002t0002g0223 a0001c0002t0002g0282 a0001c0002t0002g0286 |
3 | HG00323.hp2 HG01168.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1507-369T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754504 | |||||||
| chr4:26754596 | G | C | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1507-277G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754596 | |||||||
| chr4:26754649 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1507-224A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754649 | |||||||
| chr4:26754681 | C | T | 1 | a0001c0002t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1507-192C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754681 |