Search by Gene
| Item | Value |
|---|---|
| geneid | 4943 |
| ensemblid | ENSG00000068354.16 |
| hgncid | 8092 |
| symbol | TBC1D25 |
| name | TBC1 domain family member 25 |
| refseq_nuc | NM_002536.4 |
| refseq_prot | NP_002527.1 |
| ensembl_nuc | ENST00000376771.9 |
| ensembl_prot | ENSP00000365962.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 48539714 |
| end | 48562609 |
| strand | + |
| ver | v1.2 |
| region | chrX:48539714-48562609 |
| region5000 | chrX:48534714-48567609 |
| regionname0 | TBC1D25_chrX_48539714_48562609 |
| regionname5000 | TBC1D25_chrX_48534714_48567609 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 688 | 160 | 60 | 24 | 61 | 4 | 11 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | MATAS others(683): Show |
chrX | 48534714 | 48567609 |
| a0002 | 0/0 | 688 | 128 | 19 | 26 | 57 | 5 | 21 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | MATAS others(683): Show |
chrX | 48534714 | 48567609 |
| a0003 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | MATAS others(683): Show |
chrX | 48534714 | 48567609 |
| a0004 | 0/0 | 91 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | MATAS others(86): Show |
chrX | 48534714 | 48567609 |
| a0005 | 0/0 | 686 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | MATAS others(681): Show |
chrX | 48534714 | 48567609 |
| a0006 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | MATAS others(573): Show |
chrX | 48534714 | 48567609 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2064 | 157 | 60 | 24 | 61 | 2 | 10 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0001c0003 | 0/0 | 2064 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0001c0008 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0002c0002 | 0/0 | 2064 | 126 | 19 | 26 | 57 | 5 | 19 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0002c0006 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0002c0007 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0003c0009 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2059): Show |
chrX | 48534714 | 48567609 | ||
| a0004c0004 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2058): Show |
chrX | 48534714 | 48567609 | ||
| a0005c0010 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2053): Show |
chrX | 48534714 | 48567609 | ||
| a0006c0005 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | ATGGC others(2058): Show |
chrX | 48534714 | 48567609 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3785 | 114 | 25 | 18 | 60 | 2 | 9 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0001c0001t0002 | 0/0 | 3785 | 40 | 34 | 6 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0001c0001t0005 | 0/0 | 3785 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0001c0001t0007 | 0/0 | 3785 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0001c0001t0009 | 0/0 | 3785 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0001c0003t0001 | 0/0 | 3785 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0001c0008t0001 | 0/0 | 3785 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0001 | 0/0 | 3785 | 115 | 18 | 24 | 52 | 5 | 16 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0003 | 0/0 | 3786 | 3 | 0 | 1 | 1 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3781): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0004 | 0/0 | 3785 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0006 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3781): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0008 | 0/0 | 3785 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0010 | 0/0 | 3785 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0012 | 0/0 | 3785 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0013 | 0/0 | 3785 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0002t0014 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3781): Show |
chrX | 48534714 | 48567609 |
| a0002c0006t0001 | 0/0 | 3785 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0002c0007t0001 | 0/0 | 3785 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0003c0009t0002 | 0/0 | 3785 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3780): Show |
chrX | 48534714 | 48567609 |
| a0004c0004t0001 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3779): Show |
chrX | 48534714 | 48567609 |
| a0005c0010t0011 | 0/0 | 3778 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3773): Show |
chrX | 48534714 | 48567609 |
| a0006c0005t0001 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | GGGGC others(3779): Show |
chrX | 48534714 | 48567609 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 2 | 2 | 11 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0004 | 0/0 | 8 | 2 | 1 | 5 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0001c0008t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0002 | 0/0 | 11 | 1 | 4 | 4 | 0 | 2 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0003 | 0/0 | 7 | 2 | 1 | 1 | 0 | 3 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0019 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0003g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0004g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0010g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0013g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0002t0014g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0002c0007t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0003c0009t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0005c0010t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| a0006c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0090 | EUR | GBR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0086 | EUR | GBR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0108 | EUR | GBR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0025 | EUR | FIN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | FIN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00673 | hp1 | a0002 | c0002 | t0013 | g0104 | EAS | CHS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01074 | hp1 | a0002 | c0002 | t0004 | g0003 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0025 | EUR | IBS | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | CDX | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0173 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02683 | hp2 | a0002 | c0002 | t0010 | g0002 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02735 | hp1 | a0001 | c0008 | t0001 | g0185 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03130 | hp1 | a0003 | c0009 | t0002 | g0136 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0194 | AFR | ESN | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03579 | hp1 | a0002 | c0002 | t0012 | g0116 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03669 | hp2 | a0002 | c0007 | t0001 | g0117 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0128 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03927 | hp1 | a0002 | c0006 | t0001 | g0088 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0110 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0101 | SAS | STU | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18989 | hp1 | a0002 | c0002 | t0008 | g0084 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19001 | hp1 | a0004 | c0004 | t0001 | g0033 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19001 | hp2 | a0002 | c0002 | t0014 | g0203 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19003 | hp1 | a0002 | c0002 | t0006 | g0202 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | LWK | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19072 | hp1 | a0005 | c0010 | t0011 | g0179 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19075 | hp1 | a0006 | c0005 | t0001 | g0113 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0099 | EUR | TSI | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | GIH | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | USA | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | USA | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | USA | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | LWK | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | TBC1D25_chrX_48534714_48567609 | TBC1D25 | chrX | 48534714 | 48567609 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:48544900 | CG | C | 1 | a0004 | 1 | NA19001.hp1 | frameshift_variant | HIGH | c.268delG | p.Asp90fs | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/6 | 352/3785 | 268/2067 | 90/688 | INFO_REALIGN_3_PRIME | chrX | 48544900 | ||
| chrX:48559738 | A | G | 4 | a0001a0003a0004others(1): Show | 163 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
missense_variant | MODERATE | c.830A>G | p.Asn277Ser | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 914/3785 | 830/2067 | 277/688 | chrX | 48559738 | |||
| chrX:48560271 | G | A | 4 | a0001a0003a0004others(1): Show | 163 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
missense_variant | MODERATE | c.1363G>A | p.Ala455Thr | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1447/3785 | 1363/2067 | 455/688 | chrX | 48560271 | |||
| chrX:48560380 | CCAGTCA | C | 1 | a0005 | 1 | NA19072.hp1 | disruptive_inframe_deletion | MODERATE | c.1473_1478delCAGTCA | p.Ser492_Gln493del | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1557/3785 | 1473/2067 | 491/688 | chrX | 48560380 | |||
| chrX:48560571 | TC | T | 1 | a0006 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1666delC | p.His556fs | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1750/3785 | 1666/2067 | 556/688 | INFO_REALIGN_3_PRIME | chrX | 48560571 | ||
| chrX:48560745 | C | T | 1 | a0003 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1837C>T | p.Arg613Trp | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1921/3785 | 1837/2067 | 613/688 | chrX | 48560745 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:48559322 | C | T | 1 | a0001c0003 | 2 | HG00280.hp1 HG01515.hp1 |
synonymous_variant | LOW | c.681C>T | p.Gly227Gly | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 5/6 | 765/3785 | 681/2067 | 227/688 | chrX | 48559322 | |||
| chrX:48559811 | C | T | 1 | a0002c0007 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.903C>T | p.Tyr301Tyr | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 987/3785 | 903/2067 | 301/688 | chrX | 48559811 | |||
| chrX:48560636 | T | C | 1 | a0002c0006 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1728T>C | p.Asp576Asp | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1812/3785 | 1728/2067 | 576/688 | chrX | 48560636 | |||
| chrX:48560966 | C | T | 1 | a0001c0008 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.2058C>T | p.Ala686Ala | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 2142/3785 | 2058/2067 | 686/688 | chrX | 48560966 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:48539721 | C | CG | 1 | a0002c0002t0014 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | 73 | INFO_REALIGN_3_PRIME | chrX | 48539721 | |||||
| chrX:48539726 | G | A | 1 | a0001c0001t0005 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | 72 | chrX | 48539726 | ||||||
| chrX:48539748 | C | CG | 1 | a0002c0002t0006 | 1 | NA19003.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | 45 | INFO_REALIGN_3_PRIME | chrX | 48539748 | |||||
| chrX:48539752 | G | T | 1 | a0002c0002t0014 | 1 | NA19001.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | chrX | 48539752 | |||||||
| chrX:48539753 | T | G | 1 | a0002c0002t0014 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-45T>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | 45 | chrX | 48539753 | ||||||
| chrX:48539753 | T | TG | 1 | a0002c0002t0003 | 3 | HG01081.hp2 HG02523.hp2 HG03831.hp1 |
5_prime_UTR_variant | MODIFIER | c.-39dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | 38 | INFO_REALIGN_3_PRIME | chrX | 48539753 | |||||
| chrX:48539754 | G | C | 1 | a0001c0001t0007 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/6 | 44 | chrX | 48539754 | ||||||
| chrX:48561027 | A | G | 1 | a0002c0002t0013 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 52 | chrX | 48561027 | ||||||
| chrX:48561448 | G | A | 1 | a0002c0002t0008 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*473G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 473 | chrX | 48561448 | ||||||
| chrX:48561777 | T | C | 1 | a0001c0001t0009 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 802 | chrX | 48561777 | ||||||
| chrX:48562329 | G | T | 1 | a0002c0002t0012 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1354 | chrX | 48562329 | ||||||
| chrX:48562353 | G | A | 3 | a0001c0001t0002a0001c0001t0009a0003c0009t0002 | 42 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1378G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1378 | chrX | 48562353 | ||||||
| chrX:48562377 | G | A | 1 | a0002c0002t0010 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1402G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1402 | chrX | 48562377 | ||||||
| chrX:48562493 | C | T | 1 | a0002c0002t0004 | 2 | HG01074.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1518C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1518 | chrX | 48562493 | ||||||
| chrX:48562530 | AG | A | 1 | a0005c0010t0011 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1558delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1558 | INFO_REALIGN_3_PRIME | chrX | 48562530 | |||||
| chrX:48562546 | T | TG | 1 | a0005c0010t0011 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1574dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1575 | INFO_REALIGN_3_PRIME | chrX | 48562546 | |||||
| chrX:48562600 | TA | T | 1 | a0005c0010t0011 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1627delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 6/6 | 1627 | INFO_REALIGN_3_PRIME | chrX | 48562600 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:48539941 | G | GC | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.123+24dupC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48539941 | ||||||
| chrX:48539967 | A | AG | 1 | a0002c0002t0006g0202 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.123+52dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48539967 | ||||||
| chrX:48540016 | G | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0030others(8): Show | 15 | HG00438.hp2 HG00558.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.123+96G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48540016 | |||||||
| chrX:48540029 | G | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01123.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.123+109G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48540029 | |||||||
| chrX:48540361 | CG | C | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+443delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540361 | ||||||
| chrX:48540508 | AG | A | 2 | a0002c0002t0001g0039a0002c0002t0014g0203 | 2 | NA18992.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.123+590delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540508 | ||||||
| chrX:48540561 | GT | G | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.123+643delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540561 | ||||||
| chrX:48540563 | TC | T | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+646delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540563 | ||||||
| chrX:48540601 | G | GGTGA | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+682_123+683ins others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540601 | ||||||
| chrX:48540605 | A | AG | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+686dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540605 | ||||||
| chrX:48540628 | G | T | 2 | a0002c0002t0001g0198a0002c0002t0001g0199 | 2 | HG01261.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.124-705G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48540628 | |||||||
| chrX:48540722 | C | T | 2 | a0002c0002t0001g0196a0002c0002t0001g0197 | 2 | HG01168.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.124-611C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48540722 | |||||||
| chrX:48540790 | G | A | 1 | a0002c0002t0001g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124-543G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48540790 | |||||||
| chrX:48540808 | GA | G | 1 | a0001c0001t0001g0195 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.124-519delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540808 | ||||||
| chrX:48540832 | G | GC | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.124-500dupC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540832 | ||||||
| chrX:48540870 | A | C | 1 | a0001c0001t0009g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.124-463A>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48540870 | |||||||
| chrX:48540913 | CA | C | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.124-418delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540913 | ||||||
| chrX:48540949 | T | TA | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.124-381dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540949 | ||||||
| chrX:48540956 | CA | C | 1 | a0001c0001t0001g0195 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.124-371delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48540956 | ||||||
| chrX:48541087 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.124-246G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48541087 | |||||||
| chrX:48541134 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.124-199T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48541134 | |||||||
| chrX:48541159 | T | C | 4 | a0001c0001t0002g0005a0001c0001t0002g0042a0001c0001t0002g0043others(1): Show | 9 | HG01081.hp1 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-174T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48541159 | |||||||
| chrX:48541278 | T | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(15): Show | 23 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-55T>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48541278 | |||||||
| chrX:48541279 | CT | C | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.124-52delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48541279 | ||||||
| chrX:48541325 | C | T | 1 | a0002c0002t0001g0192 | 1 | NA19058.hp1 | splice_region_variant&intron_variant | LOW | c.124-8C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | chrX | 48541325 | |||||||
| chrX:48541326 | TC | T | 1 | a0002c0002t0001g0059 | 1 | HG01169.hp2 | splice_region_variant&intron_variant | LOW | c.124-3delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 48541326 | ||||||
| chrX:48541608 | GT | G | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.233+170delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48541608 | ||||||
| chrX:48541738 | CA | C | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.233+298delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48541738 | ||||||
| chrX:48541762 | AT | A | 1 | a0001c0001t0001g0061 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.233+325delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48541762 | ||||||
| chrX:48541768 | CA | C | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.233+328delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48541768 | ||||||
| chrX:48541826 | C | A | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG02055.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.233+384C>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48541826 | |||||||
| chrX:48541863 | T | G | 1 | a0002c0002t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.233+421T>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48541863 | |||||||
| chrX:48541884 | C | CA | 1 | a0001c0001t0001g0061 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.233+443dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48541884 | ||||||
| chrX:48542016 | CT | C | 1 | a0001c0001t0001g0061 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.233+579delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542016 | ||||||
| chrX:48542026 | C | CT | 18 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0046others(15): Show | 21 | HG00741.hp1 HG01070.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.233+601dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542026 | ||||||
| chrX:48542026 | C | CTT | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(87): Show | 138 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.233+600_233+601dup others(2): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542026 | ||||||
| chrX:48542026 | C | CTTT | 5 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0191others(2): Show | 5 | HG01346.hp1 HG01346.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+599_233+601dup others(3): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542026 | ||||||
| chrX:48542026 | CT | C | 7 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0068others(4): Show | 7 | HG01123.hp1 HG01943.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+601delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542026 | ||||||
| chrX:48542165 | A | AT | 60 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(57): Show | 98 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.233+743dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542165 | ||||||
| chrX:48542165 | A | ATT | 1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+742_233+743dup others(2): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542165 | ||||||
| chrX:48542165 | AT | A | 18 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0002g0062others(15): Show | 23 | HG01168.hp1 HG01255.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+743delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542165 | ||||||
| chrX:48542191 | G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0134a0001c0001t0002g0135others(5): Show | 10 | HG00741.hp1 HG01070.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.233+749G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48542191 | |||||||
| chrX:48542261 | C | CG | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.233+822dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542261 | ||||||
| chrX:48542334 | AT | A | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.233+897delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542334 | ||||||
| chrX:48542341 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.233+899T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48542341 | |||||||
| chrX:48542365 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.233+923A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48542365 | |||||||
| chrX:48542370 | GT | G | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.233+930delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542370 | ||||||
| chrX:48542419 | CG | C | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.233+979delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542419 | ||||||
| chrX:48542490 | C | CTT | 1 | a0002c0002t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.233+1061_233+1062d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542490 | ||||||
| chrX:48542490 | CT | C | 5 | a0001c0001t0001g0032a0001c0001t0002g0042a0002c0002t0001g0060others(2): Show | 5 | HG01081.hp1 HG02896.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+1062delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542490 | ||||||
| chrX:48542531 | AG | A | 1 | a0002c0002t0001g0066 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.233+1091delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542531 | ||||||
| chrX:48542620 | TG | T | 1 | a0002c0002t0001g0066 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.233+1181delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542620 | ||||||
| chrX:48542663 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.233+1221A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48542663 | |||||||
| chrX:48542705 | C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.233+1263C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48542705 | |||||||
| chrX:48542758 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.233+1316C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48542758 | |||||||
| chrX:48542868 | TG | T | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.233+1429delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542868 | ||||||
| chrX:48542931 | T | TA | 7 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0079others(4): Show | 7 | HG02135.hp1 NA18947.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+1490dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48542931 | ||||||
| chrX:48543122 | CG | C | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.233+1687delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543122 | ||||||
| chrX:48543246 | A | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-1623A>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543246 | |||||||
| chrX:48543246 | AT | A | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-1613delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543246 | ||||||
| chrX:48543345 | T | TC | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234-1522dupC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543345 | ||||||
| chrX:48543372 | T | G | 1 | a0001c0001t0002g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.234-1497T>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543372 | |||||||
| chrX:48543452 | G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.234-1417G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543452 | |||||||
| chrX:48543471 | G | A | 3 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | HG02257.hp2 HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.234-1398G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543471 | |||||||
| chrX:48543487 | A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.234-1382A>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543487 | |||||||
| chrX:48543537 | CT | C | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234-1327delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543537 | ||||||
| chrX:48543631 | TC | T | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-1235delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543631 | ||||||
| chrX:48543642 | TG | T | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-1224delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543642 | ||||||
| chrX:48543644 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.234-1225G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543644 | |||||||
| chrX:48543682 | A | AG | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234-1186dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543682 | ||||||
| chrX:48543757 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.234-1112G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543757 | |||||||
| chrX:48543805 | G | GC | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234-1061dupC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543805 | ||||||
| chrX:48543809 | G | A | 1 | a0002c0002t0001g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.234-1060G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543809 | |||||||
| chrX:48543816 | G | A | 3 | a0002c0002t0001g0011a0002c0002t0001g0071a0002c0002t0001g0072 | 5 | HG02723.hp1 HG02896.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1053G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543816 | |||||||
| chrX:48543870 | T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.234-999T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543870 | |||||||
| chrX:48543871 | G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.234-998G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543871 | |||||||
| chrX:48543883 | C | CA | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.234-971dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543883 | ||||||
| chrX:48543883 | C | CAA | 27 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 36 | HG00438.hp2 HG00741.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.234-972_234-971dup others(2): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543883 | ||||||
| chrX:48543883 | C | CAAA | 1 | a0002c0002t0008g0084 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.234-973_234-971dup others(3): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543883 | ||||||
| chrX:48543883 | CA | C | 2 | a0002c0002t0001g0196a0002c0002t0014g0203 | 2 | HG01168.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.234-971delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543883 | ||||||
| chrX:48543923 | A | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0200others(1): Show | 4 | HG01123.hp2 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-946A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48543923 | |||||||
| chrX:48543946 | A | AC | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234-920dupC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48543946 | ||||||
| chrX:48544008 | G | C | 2 | a0001c0001t0002g0163a0001c0001t0002g0190 | 2 | HG01346.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.234-861G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48544008 | |||||||
| chrX:48544068 | A | G | 27 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0039others(24): Show | 35 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.234-801A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48544068 | |||||||
| chrX:48544221 | GT | G | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-646delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544221 | ||||||
| chrX:48544248 | C | CT | 1 | a0002c0002t0001g0066 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.234-612dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544248 | ||||||
| chrX:48544248 | C | CTT | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-613_234-612dup others(2): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544248 | ||||||
| chrX:48544248 | CT | C | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.234-612delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544248 | ||||||
| chrX:48544317 | A | C | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-552A>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48544317 | |||||||
| chrX:48544319 | C | A | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-550C>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48544319 | |||||||
| chrX:48544319 | C | CT | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(52): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.234-534dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544319 | ||||||
| chrX:48544319 | C | CTT | 4 | a0001c0001t0001g0037a0001c0001t0001g0061a0001c0001t0001g0187others(1): Show | 4 | HG01109.hp1 HG01358.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-535_234-534dup others(2): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544319 | ||||||
| chrX:48544320 | T | C | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-549T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48544320 | |||||||
| chrX:48544484 | A | AT | 1 | a0001c0001t0001g0186 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.234-377dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544484 | ||||||
| chrX:48544513 | G | GT | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234-353dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544513 | ||||||
| chrX:48544613 | A | AC | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234-253dupC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chrX | 48544613 | ||||||
| chrX:48544736 | T | G | 1 | a0002c0002t0001g0012 | 3 | HG02083.hp1 NA18959.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.234-133T>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 2/5 | chrX | 48544736 | |||||||
| chrX:48545168 | A | AT | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+148dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48545168 | ||||||
| chrX:48545243 | G | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(49): Show | 65 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.388+220G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48545243 | |||||||
| chrX:48545333 | A | AT | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388+311dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48545333 | ||||||
| chrX:48545338 | A | T | 1 | a0002c0007t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.388+315A>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48545338 | |||||||
| chrX:48545396 | A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(15): Show | 23 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+373A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48545396 | |||||||
| chrX:48545619 | G | A | 34 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0021others(31): Show | 42 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.388+596G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48545619 | |||||||
| chrX:48545647 | T | C | 1 | a0002c0002t0001g0132 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.388+624T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48545647 | |||||||
| chrX:48545712 | CT | C | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+691delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48545712 | ||||||
| chrX:48545822 | TG | T | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.388+801delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48545822 | ||||||
| chrX:48546047 | TA | T | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+1032delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546047 | ||||||
| chrX:48546070 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.388+1047G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48546070 | |||||||
| chrX:48546168 | T | C | 1 | a0003c0009t0002g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388+1145T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48546168 | |||||||
| chrX:48546212 | C | CA | 13 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0008t0001g0185others(10): Show | 20 | HG01123.hp1 HG01255.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.388+1206dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546212 | ||||||
| chrX:48546212 | C | CAA | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(72): Show | 116 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.388+1205_388+1206d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546212 | ||||||
| chrX:48546212 | C | CAAA | 2 | a0001c0001t0001g0050a0001c0001t0001g0169 | 2 | NA18949.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.388+1204_388+1206d others(5): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546212 | ||||||
| chrX:48546260 | TC | T | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.388+1240delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546260 | ||||||
| chrX:48546280 | G | A | 3 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156 | 3 | HG02647.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.388+1257G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48546280 | |||||||
| chrX:48546290 | G | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.388+1267G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48546290 | |||||||
| chrX:48546327 | C | T | 1 | a0002c0002t0012g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.388+1304C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48546327 | |||||||
| chrX:48546375 | T | TG | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+1354dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546375 | ||||||
| chrX:48546515 | AAAAT | A | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388+1500_388+1503d others(6): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546515 | ||||||
| chrX:48546552 | TC | T | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.388+1532delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546552 | ||||||
| chrX:48546681 | T | TG | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+1660dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546681 | ||||||
| chrX:48546963 | A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.388+1940A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48546963 | |||||||
| chrX:48546980 | TG | T | 1 | a0002c0002t0014g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.388+1960delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48546980 | ||||||
| chrX:48547163 | A | AG | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+2142dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547163 | ||||||
| chrX:48547314 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.388+2291G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48547314 | |||||||
| chrX:48547431 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.388+2408G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48547431 | |||||||
| chrX:48547485 | A | AG | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+2463dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547485 | ||||||
| chrX:48547545 | GAAA | G | 1 | a0002c0002t0001g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.388+2524_388+2526d others(5): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547545 | ||||||
| chrX:48547573 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.388+2550C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48547573 | |||||||
| chrX:48547592 | GAGAC | G | 4 | a0002c0002t0001g0018a0002c0002t0001g0077a0002c0002t0001g0095others(1): Show | 5 | HG00639.hp1 HG01256.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+2577_388+2580d others(6): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547592 | ||||||
| chrX:48547608 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.388+2585C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48547608 | |||||||
| chrX:48547736 | A | AG | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+2714dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547736 | ||||||
| chrX:48547758 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.388+2735C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48547758 | |||||||
| chrX:48547798 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.388+2775C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48547798 | |||||||
| chrX:48547937 | C | CA | 9 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0172others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+2932dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547937 | ||||||
| chrX:48547937 | CA | C | 3 | a0001c0001t0001g0058a0002c0002t0014g0203a0006c0005t0001g0113 | 3 | HG03490.hp1 NA19001.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.388+2932delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48547937 | ||||||
| chrX:48548074 | T | TA | 1 | a0001c0001t0001g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.388+3052dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548074 | ||||||
| chrX:48548100 | T | TTTGG | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.388+3078_388+3079i others(6): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548100 | ||||||
| chrX:48548112 | G | GT | 7 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0184others(4): Show | 8 | HG02572.hp1 NA19003.hp1 NA19006.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+3099dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548112 | ||||||
| chrX:48548112 | GT | G | 1 | a0002c0002t0001g0119 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.388+3099delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548112 | ||||||
| chrX:48548122 | T | TTG | 1 | a0002c0002t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.388+3099_388+3100i others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48548122 | |||||||
| chrX:48548123 | G | GT | 8 | a0001c0001t0001g0183a0001c0001t0002g0063a0002c0002t0001g0067others(5): Show | 8 | HG00423.hp1 HG02055.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+3110dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548123 | ||||||
| chrX:48548123 | G | T | 1 | a0002c0002t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.388+3100G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48548123 | |||||||
| chrX:48548454 | CT | C | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.388+3436delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548454 | ||||||
| chrX:48548658 | T | C | 1 | a0002c0002t0001g0120 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.388+3635T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48548658 | |||||||
| chrX:48548685 | C | CT | 1 | a0001c0001t0001g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.388+3667dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48548685 | ||||||
| chrX:48548752 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.388+3729C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48548752 | |||||||
| chrX:48549409 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.388+4386G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48549409 | |||||||
| chrX:48549471 | A | G | 1 | a0002c0002t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.388+4448A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48549471 | |||||||
| chrX:48549721 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.388+4698G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48549721 | |||||||
| chrX:48549838 | A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0148 | 2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.388+4815A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48549838 | |||||||
| chrX:48549992 | A | AT | 1 | a0006c0005t0001g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+4980dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48549992 | ||||||
| chrX:48549992 | ATT | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.388+4979_388+4980d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48549992 | ||||||
| chrX:48550119 | TG | T | 1 | a0001c0001t0001g0174 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.388+5099delG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48550119 | ||||||
| chrX:48550330 | C | T | 1 | a0002c0002t0001g0091 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.388+5307C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550330 | |||||||
| chrX:48550413 | T | C | 1 | a0002c0007t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.388+5390T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550413 | |||||||
| chrX:48550429 | AC | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(15): Show | 23 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+5407delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550429 | |||||||
| chrX:48550431 | T | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(15): Show | 23 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+5408T>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550431 | |||||||
| chrX:48550432 | G | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(15): Show | 23 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+5409G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550432 | |||||||
| chrX:48550433 | C | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(15): Show | 23 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+5410C>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550433 | |||||||
| chrX:48550451 | AT | A | 1 | a0001c0001t0001g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.388+5433delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48550451 | ||||||
| chrX:48550479 | A | AT | 3 | a0001c0001t0001g0055a0001c0001t0002g0063a0002c0002t0001g0109 | 3 | HG02055.hp1 NA18942.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.388+5471dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48550479 | ||||||
| chrX:48550479 | A | T | 1 | a0006c0005t0001g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+5456A>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550479 | |||||||
| chrX:48550479 | AT | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0175a0002c0002t0001g0071 | 3 | HG02896.hp1 NA18947.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.388+5471delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48550479 | ||||||
| chrX:48550499 | T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.388+5476T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550499 | |||||||
| chrX:48550525 | G | A | 3 | a0002c0002t0001g0012a0002c0002t0001g0066a0002c0002t0001g0097 | 5 | HG02083.hp1 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+5502G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550525 | |||||||
| chrX:48550570 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.388+5547G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550570 | |||||||
| chrX:48550593 | C | T | 14 | a0001c0001t0002g0013a0001c0001t0002g0134a0001c0001t0002g0135others(11): Show | 16 | HG00741.hp1 HG01070.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.388+5570C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550593 | |||||||
| chrX:48550661 | C | CT | 4 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0055others(1): Show | 4 | NA18949.hp2 NA18972.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+5653dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48550661 | ||||||
| chrX:48550661 | CT | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0176a0001c0001t0002g0155others(1): Show | 4 | HG00323.hp2 HG03041.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+5653delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48550661 | ||||||
| chrX:48550910 | C | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0134a0001c0001t0002g0135others(3): Show | 8 | HG00741.hp1 HG01070.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+5887C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550910 | |||||||
| chrX:48550939 | A | G | 1 | a0002c0002t0001g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.388+5916A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48550939 | |||||||
| chrX:48551227 | C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0181a0001c0001t0001g0182 | 4 | HG01934.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+6204C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551227 | |||||||
| chrX:48551327 | TTTTG | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(49): Show | 65 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.388+6324_388+6327d others(6): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48551327 | ||||||
| chrX:48551624 | CT | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.388+6609delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48551624 | ||||||
| chrX:48551650 | G | C | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.388+6627G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551650 | |||||||
| chrX:48551677 | G | A | 1 | a0001c0008t0001g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.388+6654G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551677 | |||||||
| chrX:48551699 | C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.388+6676C>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551699 | |||||||
| chrX:48551704 | AC | A | 1 | a0001c0001t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.388+6685delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48551704 | ||||||
| chrX:48551765 | C | T | 2 | a0002c0002t0001g0127a0002c0002t0003g0128 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.388+6742C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551765 | |||||||
| chrX:48551862 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388+6839C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551862 | |||||||
| chrX:48551939 | G | A | 13 | a0001c0001t0002g0021a0001c0001t0002g0062a0001c0001t0002g0063others(10): Show | 14 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.388+6916G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48551939 | |||||||
| chrX:48552059 | C | T | 5 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-6838C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48552059 | |||||||
| chrX:48552104 | A | G | 1 | a0002c0002t0001g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.389-6793A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48552104 | |||||||
| chrX:48552188 | C | CT | 1 | a0002c0002t0001g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.389-6699dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552188 | ||||||
| chrX:48552228 | CCAG | C | 1 | a0001c0001t0002g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.389-6668_389-6666d others(5): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48552228 | |||||||
| chrX:48552344 | GC | G | 1 | a0001c0001t0001g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.389-6550delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552344 | ||||||
| chrX:48552353 | A | AT | 3 | a0001c0001t0001g0171a0001c0001t0001g0180a0002c0002t0001g0107 | 3 | HG01169.hp1 HG04184.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.389-6525dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552353 | ||||||
| chrX:48552353 | AT | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0032others(59): Show | 75 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.389-6525delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552353 | ||||||
| chrX:48552393 | C | T | 1 | a0002c0002t0001g0066 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.389-6504C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48552393 | |||||||
| chrX:48552630 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.389-6267C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48552630 | |||||||
| chrX:48552648 | GC | G | 1 | a0001c0001t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.389-6245delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552648 | ||||||
| chrX:48552687 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.389-6210A>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48552687 | |||||||
| chrX:48552793 | C | CT | 2 | a0002c0002t0001g0068a0002c0002t0001g0107 | 2 | HG04184.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.389-6090dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552793 | ||||||
| chrX:48552793 | CT | C | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.389-6090delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552793 | ||||||
| chrX:48552879 | TC | T | 1 | a0002c0002t0001g0139 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.389-6015delC | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552879 | ||||||
| chrX:48552971 | G | GT | 1 | a0002c0002t0001g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.389-5925dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48552971 | ||||||
| chrX:48553135 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.389-5762C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48553135 | |||||||
| chrX:48553199 | A | G | 1 | a0003c0009t0002g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.389-5698A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48553199 | |||||||
| chrX:48553251 | AATATAAT | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.389-5632_389-5626d others(9): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48553251 | ||||||
| chrX:48553616 | C | CT | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 94 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.389-5259dupT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48553616 | ||||||
| chrX:48553616 | C | CTT | 7 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0038others(4): Show | 9 | HG00423.hp1 HG00609.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.389-5260_389-5259d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48553616 | ||||||
| chrX:48553616 | CT | C | 93 | a0001c0001t0001g0054a0001c0001t0002g0005a0001c0001t0002g0013others(90): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.389-5259delT | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48553616 | ||||||
| chrX:48553616 | CTT | C | 3 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | HG02257.hp2 HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.389-5260_389-5259d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48553616 | ||||||
| chrX:48553720 | G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 99 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.389-5177G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48553720 | |||||||
| chrX:48553947 | G | A | 2 | a0002c0002t0001g0101a0002c0002t0001g0102 | 2 | HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.389-4950G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48553947 | |||||||
| chrX:48554010 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG02071.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.389-4887G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48554010 | |||||||
| chrX:48554049 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-4848C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48554049 | |||||||
| chrX:48554125 | G | A | 2 | a0002c0002t0001g0122a0002c0002t0001g0129 | 2 | NA18984.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.389-4772G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48554125 | |||||||
| chrX:48554180 | CA | C | 1 | a0004c0004t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.389-4705delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48554180 | ||||||
| chrX:48554228 | T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.389-4669T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48554228 | |||||||
| chrX:48554559 | C | CA | 6 | a0001c0001t0002g0063a0002c0002t0001g0087a0002c0002t0001g0093others(3): Show | 6 | HG00423.hp2 HG01175.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-4319dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48554559 | ||||||
| chrX:48554559 | CA | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(63): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.389-4319delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48554559 | ||||||
| chrX:48554559 | CAA | C | 2 | a0001c0001t0001g0142a0005c0010t0011g0179 | 2 | NA18992.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.389-4320_389-4319d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48554559 | ||||||
| chrX:48555212 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.389-3685A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48555212 | |||||||
| chrX:48555222 | G | A | 1 | a0002c0002t0001g0095 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.389-3675G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48555222 | |||||||
| chrX:48555334 | C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.389-3563C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48555334 | |||||||
| chrX:48555476 | G | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0064 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.389-3421G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48555476 | |||||||
| chrX:48555564 | T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.389-3333T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48555564 | |||||||
| chrX:48555784 | CAT | C | 1 | a0002c0002t0001g0198 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.389-3112_389-3111d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48555784 | |||||||
| chrX:48555877 | C | CA | 1 | a0006c0005t0001g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.389-3017dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48555877 | ||||||
| chrX:48556048 | A | G | 1 | a0002c0002t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.389-2849A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556048 | |||||||
| chrX:48556060 | A | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.389-2837A>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556060 | |||||||
| chrX:48556099 | A | G | 7 | a0002c0002t0001g0041a0002c0002t0001g0067a0002c0002t0001g0079others(4): Show | 7 | HG02135.hp1 NA18947.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.389-2798A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556099 | |||||||
| chrX:48556202 | G | GGCAGA | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.389-2693_389-2689d others(7): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48556202 | ||||||
| chrX:48556209 | T | C | 1 | a0002c0002t0001g0085 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.389-2688T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556209 | |||||||
| chrX:48556309 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.389-2588C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556309 | |||||||
| chrX:48556521 | T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 163 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.389-2376T>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556521 | |||||||
| chrX:48556607 | C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0144a0001c0001t0001g0174 | 4 | HG01070.hp1 HG01071.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-2290C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556607 | |||||||
| chrX:48556746 | C | CA | 17 | a0002c0002t0001g0068a0002c0002t0001g0072a0002c0002t0001g0075others(14): Show | 17 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.389-2129dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48556746 | ||||||
| chrX:48556746 | CA | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0048a0001c0001t0001g0143others(13): Show | 18 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.389-2129delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48556746 | ||||||
| chrX:48556746 | CAA | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(93): Show | 145 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.389-2130_389-2129d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48556746 | ||||||
| chrX:48556746 | CAAA | C | 1 | a0001c0001t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.389-2131_389-2129d others(5): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48556746 | ||||||
| chrX:48556922 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.389-1975G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48556922 | |||||||
| chrX:48557010 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.389-1887C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557010 | |||||||
| chrX:48557063 | C | CA | 28 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(25): Show | 34 | HG00280.hp1 HG00558.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.389-1820dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48557063 | ||||||
| chrX:48557063 | C | CAA | 1 | a0001c0001t0001g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.389-1821_389-1820d others(4): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48557063 | ||||||
| chrX:48557063 | CA | C | 2 | a0001c0001t0001g0030a0006c0005t0001g0113 | 2 | NA18949.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.389-1820delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48557063 | ||||||
| chrX:48557094 | G | A | 1 | a0002c0002t0001g0096 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.389-1803G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557094 | |||||||
| chrX:48557142 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.389-1755C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557142 | |||||||
| chrX:48557638 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.389-1259C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557638 | |||||||
| chrX:48557643 | C | CA | 7 | a0001c0001t0001g0061a0001c0001t0002g0005a0001c0001t0002g0042others(4): Show | 12 | HG01081.hp1 HG01978.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.389-1238dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48557643 | ||||||
| chrX:48557643 | CA | C | 1 | a0002c0002t0001g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.389-1238delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48557643 | ||||||
| chrX:48557730 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.389-1167A>G | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557730 | |||||||
| chrX:48557742 | G | A | 1 | a0002c0002t0001g0129 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.389-1155G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557742 | |||||||
| chrX:48557764 | G | T | 34 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0021others(31): Show | 42 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.389-1133G>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557764 | |||||||
| chrX:48557808 | CA | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 163 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.389-1079delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48557808 | ||||||
| chrX:48557892 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.389-1005C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48557892 | |||||||
| chrX:48558013 | A | AG | 1 | a0005c0010t0011g0179 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.389-882dupG | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48558013 | ||||||
| chrX:48558051 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.389-846C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48558051 | |||||||
| chrX:48558111 | C | CA | 59 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0026others(56): Show | 74 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.389-768dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48558111 | ||||||
| chrX:48558111 | C | CAA | 7 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0053others(4): Show | 7 | HG00544.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.389-769_389-768dup others(2): Show |
TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48558111 | ||||||
| chrX:48558111 | CA | C | 2 | a0002c0002t0001g0129a0006c0005t0001g0113 | 2 | NA19075.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.389-768delA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48558111 | ||||||
| chrX:48558196 | G | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0193 | 3 | HG02922.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.389-701G>C | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48558196 | |||||||
| chrX:48558262 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.389-635C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48558262 | |||||||
| chrX:48558552 | T | TA | 1 | a0005c0010t0011g0179 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.389-344dupA | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chrX | 48558552 | ||||||
| chrX:48558618 | C | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(46): Show | 62 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.389-279C>T | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48558618 | |||||||
| chrX:48558828 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.389-69G>A | TBC1D25 | ENSG00000068354.16 | transcript | ENST00000376771.9 | protein_coding | 3/5 | chrX | 48558828 |