Search by Gene
| Item | Value |
|---|---|
| geneid | 7993 |
| ensemblid | ENSG00000104691.16 |
| hgncid | 30307 |
| symbol | UBXN8 |
| name | UBX domain protein 8 |
| refseq_nuc | NM_005671.4 |
| refseq_prot | NP_005662.2 |
| ensembl_nuc | ENST00000265616.10 |
| ensembl_prot | ENSP00000479216.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 30744164 |
| end | 30767006 |
| strand | + |
| ver | v1.2 |
| region | chr8:30744164-30767006 |
| region5000 | chr8:30739164-30772006 |
| regionname0 | UBXN8_chr8_30744164_30767006 |
| regionname5000 | UBXN8_chr8_30739164_30772006 |
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 | 270 | 256 | 78 | 54 | 94 | 8 | 22 | UBXN8_chr8_30739164_30772006 | UBXN8 | MASRG others(265): Show |
chr8 | 30739164 | 30772006 |
| a0002 | 0/0 | 270 | 10 | 10 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | MASRG others(265): Show |
chr8 | 30739164 | 30772006 |
| a0003 | 0/0 | 28 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | MASRG others(23): Show |
chr8 | 30739164 | 30772006 |
| a0004 | 0/0 | 270 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | MASRG others(265): Show |
chr8 | 30739164 | 30772006 |
| a0006 | 0/0 | 270 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | MASRG others(265): Show |
chr8 | 30739164 | 30772006 |
| a0007 | 0/0 | 162 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | MASRG others(157): Show |
chr8 | 30739164 | 30772006 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 810 | 256 | 78 | 54 | 94 | 8 | 22 | UBXN8_chr8_30739164_30772006 | UBXN8 | ATGGC others(805): Show |
chr8 | 30739164 | 30772006 | ||
| a0002c0002 | 0/0 | 810 | 10 | 10 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | ATGGC others(805): Show |
chr8 | 30739164 | 30772006 | ||
| a0003c0003 | 0/0 | 809 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | ATGGC others(804): Show |
chr8 | 30739164 | 30772006 | ||
| a0004c0004 | 0/0 | 810 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | ATGGC others(805): Show |
chr8 | 30739164 | 30772006 | ||
| a0006c0006 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | ATGGC others(805): Show |
chr8 | 30739164 | 30772006 | ||
| a0007c0007 | 0/0 | 808 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | ATGGC others(803): Show |
chr8 | 30739164 | 30772006 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1451 | 245 | 67 | 54 | 94 | 8 | 22 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0001c0001t0002 | 0/0 | 1451 | 8 | 8 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0001c0001t0003 | 0/0 | 1451 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0001c0001t0004 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0002c0002t0001 | 0/0 | 1451 | 3 | 3 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0002c0002t0003 | 0/0 | 1451 | 7 | 7 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0003c0003t0001 | 0/0 | 1450 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1445): Show |
chr8 | 30739164 | 30772006 |
| a0004c0004t0001 | 0/0 | 1451 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0006c0006t0001 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1446): Show |
chr8 | 30739164 | 30772006 |
| a0007c0007t0001 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | CGCCT others(1444): Show |
chr8 | 30739164 | 30772006 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0002c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0004c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0006c0006t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| a0007c0007t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00408 | hp2 | a0006 | c0006 | t0001 | g0012 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0128 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0040 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0048 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0023 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0022 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0021 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0050 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0043 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19076 | hp1 | a0007 | c0007 | t0001 | g0106 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ASW | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | USA | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0026 | AFR | LWK | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | UBXN8_chr8_30739164_30772006 | UBXN8 | chr8 | 30739164 | 30772006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30744241 | G | A | 1 | a0002 | 10 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(7): Show |
missense_variant | MODERATE | c.52G>A | p.Val18Met | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/8 | 78/1451 | 52/813 | 18/270 | chr8 | 30744241 | |||
| chr8:30744269 | CG | C | 1 | a0003 | 2 | HG01099.hp1 HG01175.hp2 |
frameshift_variant | HIGH | c.82delG | p.Asp28fs | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/8 | 108/1451 | 82/813 | 28/270 | INFO_REALIGN_3_PRIME | chr8 | 30744269 | ||
| chr8:30751459 | C | T | 6 | a0001a0002a0003others(3): Show | 273 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(270): Show |
missense_variant | MODERATE | c.152C>T | p.Thr51Ile | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/8 | 178/1451 | 152/813 | 51/270 | chr8 | 30751459 | |||
| chr8:30754768 | G | A | 1 | a0004 | 2 | HG01891.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.386G>A | p.Ser129Asn | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/8 | 412/1451 | 386/813 | 129/270 | chr8 | 30754768 | |||
| chr8:30754778 | CA | C | 1 | a0007 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.399delA | p.Lys133fs | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/8 | 425/1451 | 399/813 | 133/270 | INFO_REALIGN_3_PRIME | chr8 | 30754778 | ||
| chr8:30754782 | C | T | 1 | a0006 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.400C>T | p.Leu134Phe | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/8 | 426/1451 | 400/813 | 134/270 | chr8 | 30754782 | |||
| chr8:30756836 | TA | T | 1 | a0007 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.480delA | p.Lys160fs | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/8 | 506/1451 | 480/813 | 160/270 | INFO_REALIGN_3_PRIME | chr8 | 30756836 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30766421 | A | G | 2 | a0001c0001t0003a0002c0002t0003 | 9 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*27A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 8/8 | 27 | chr8 | 30766421 | ||||||
| chr8:30766480 | T | C | 9 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*86T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 8/8 | 86 | chr8 | 30766480 | ||||||
| chr8:30766573 | G | A | 1 | a0001c0001t0004 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 8/8 | 179 | chr8 | 30766573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30744288 | C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(117): Show | 136 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.88+11C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744288 | |||||||
| chr8:30744482 | G | C | 42 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 42 | HG00621.hp2 HG01884.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.88+205G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744482 | |||||||
| chr8:30744637 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.88+360A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744637 | |||||||
| chr8:30744669 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.88+392T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744669 | |||||||
| chr8:30744719 | A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 271 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.88+442A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744719 | |||||||
| chr8:30744809 | A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 50 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.88+532A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744809 | |||||||
| chr8:30744833 | C | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(9): Show | 14 | HG02280.hp1 HG02559.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+556C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744833 | |||||||
| chr8:30744970 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.88+693T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30744970 | |||||||
| chr8:30745155 | G | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.88+878G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30745155 | |||||||
| chr8:30745306 | G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(9): Show | 14 | HG02280.hp1 HG02559.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+1029G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30745306 | |||||||
| chr8:30745592 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.88+1315A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30745592 | |||||||
| chr8:30745646 | A | C | 1 | a0001c0001t0001g0241 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.88+1369A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30745646 | |||||||
| chr8:30745842 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.88+1565G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30745842 | |||||||
| chr8:30746002 | C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.88+1725C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746002 | |||||||
| chr8:30746423 | GATATTCA others(1601): Show |
G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(48): Show | 64 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+2237_89-3275del | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30746423 | ||||||
| chr8:30746510 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+2233G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746510 | |||||||
| chr8:30746515 | A | AT | 55 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(52): Show | 57 | HG00621.hp2 HG01884.hp1 HG01891.hp1 others(54): Show |
intron_variant | MODIFIER | c.88+2248dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30746515 | ||||||
| chr8:30746515 | A | ATT | 8 | a0001c0001t0001g0060a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+2247_88+2248dup others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30746515 | ||||||
| chr8:30746525 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+2248T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746525 | |||||||
| chr8:30746526 | C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0089a0001c0001t0001g0101 | 3 | HG02109.hp2 HG02486.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.88+2249C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746526 | |||||||
| chr8:30746545 | C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02083.hp2 NA18947.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+2268C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746545 | |||||||
| chr8:30746672 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+2395A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746672 | |||||||
| chr8:30746677 | C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 176 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.88+2400C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746677 | |||||||
| chr8:30746813 | C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+2536C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746813 | |||||||
| chr8:30746891 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.88+2614T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746891 | |||||||
| chr8:30746932 | G | A | 4 | a0001c0001t0001g0013a0002c0002t0003g0021a0002c0002t0003g0022others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+2655G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746932 | |||||||
| chr8:30746948 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+2671T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30746948 | |||||||
| chr8:30746949 | AATCGAGA others(2): Show |
A | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(9): Show | 14 | HG02280.hp1 HG02559.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+2676_88+2684del others(9): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30746949 | ||||||
| chr8:30747021 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+2744G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747021 | |||||||
| chr8:30747024 | G | A | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+2747G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747024 | |||||||
| chr8:30747038 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+2761C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747038 | |||||||
| chr8:30747086 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+2809T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747086 | |||||||
| chr8:30747115 | A | G | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG03704.hp1 NA18961.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+2838A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747115 | |||||||
| chr8:30747227 | A | G | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+2950A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747227 | |||||||
| chr8:30747307 | G | GT | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.88+3051dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747307 | ||||||
| chr8:30747307 | G | GTT | 42 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0052others(39): Show | 42 | HG00735.hp2 HG01123.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+3050_88+3051dup others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747307 | ||||||
| chr8:30747307 | GT | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(14): Show | 19 | HG02280.hp1 HG02300.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+3051delT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747307 | ||||||
| chr8:30747321 | T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0242 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.88+3044T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747321 | |||||||
| chr8:30747356 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.88+3079G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747356 | |||||||
| chr8:30747454 | G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(9): Show | 14 | HG02280.hp1 HG02559.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+3177G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747454 | |||||||
| chr8:30747564 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.88+3287G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747564 | |||||||
| chr8:30747614 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88+3337A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747614 | |||||||
| chr8:30747749 | AT | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(17): Show | 22 | HG01243.hp2 HG02280.hp1 HG02300.hp2 others(19): Show |
intron_variant | MODIFIER | c.88+3482delT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747749 | ||||||
| chr8:30747768 | A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 5 | HG02723.hp2 HG02818.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+3491A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747768 | |||||||
| chr8:30747768 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.88+3491A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747768 | |||||||
| chr8:30747847 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.89-3549C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747847 | |||||||
| chr8:30747871 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-3525T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747871 | |||||||
| chr8:30747893 | TC | T | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0227others(5): Show | 8 | HG01168.hp2 HG01258.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-3502delC | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747893 | |||||||
| chr8:30747894 | C | CT | 31 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0036others(28): Show | 31 | HG00621.hp2 HG01891.hp1 HG01978.hp2 others(28): Show |
intron_variant | MODIFIER | c.89-3478dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747894 | ||||||
| chr8:30747894 | C | CTT | 5 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0206others(2): Show | 5 | HG01358.hp2 HG01496.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3479_89-3478dup others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747894 | ||||||
| chr8:30747894 | C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG02273.hp2 HG02300.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.89-3502C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747894 | |||||||
| chr8:30747894 | CT | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(27): Show | 32 | HG00735.hp2 HG01243.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.89-3478delT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747894 | ||||||
| chr8:30747894 | CTTTTTTT | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3484_89-3478del others(7): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747894 | ||||||
| chr8:30747894 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-3490_89-3478del others(13): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747894 | ||||||
| chr8:30747894 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-3491_89-3478del others(14): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30747894 | ||||||
| chr8:30747902 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.89-3494T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30747902 | |||||||
| chr8:30748122 | A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG03209.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3274A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748122 | |||||||
| chr8:30748313 | T | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 172 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.89-3083T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748313 | |||||||
| chr8:30748435 | A | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-2961A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748435 | |||||||
| chr8:30748468 | GA | G | 9 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-2914delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30748468 | ||||||
| chr8:30748508 | T | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0064others(9): Show | 14 | HG02280.hp1 HG02559.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-2888T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748508 | |||||||
| chr8:30748548 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.89-2848T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748548 | |||||||
| chr8:30748549 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.89-2847C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748549 | |||||||
| chr8:30748600 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-2796G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748600 | |||||||
| chr8:30748705 | T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02258.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.89-2691T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748705 | |||||||
| chr8:30748804 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-2592G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748804 | |||||||
| chr8:30748832 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.89-2564C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748832 | |||||||
| chr8:30748833 | G | A | 2 | a0001c0001t0001g0093a0001c0001t0002g0092 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.89-2563G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748833 | |||||||
| chr8:30748889 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-2507A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748889 | |||||||
| chr8:30748905 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.89-2491C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748905 | |||||||
| chr8:30748974 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.89-2422C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30748974 | |||||||
| chr8:30749054 | T | C | 1 | a0002c0002t0003g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.89-2342T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749054 | |||||||
| chr8:30749121 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-2275C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749121 | |||||||
| chr8:30749122 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-2274G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749122 | |||||||
| chr8:30749350 | G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0032others(19): Show | 22 | HG00621.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.89-2046G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749350 | |||||||
| chr8:30749378 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-2018C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749378 | |||||||
| chr8:30749392 | C | CAAAAA | 23 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(20): Show | 23 | HG00558.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-1996_89-1992dup others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30749392 | ||||||
| chr8:30749400 | A | AAAAAT | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(136): Show | 155 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.89-1987_89-1983dup others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30749400 | ||||||
| chr8:30749400 | A | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0049 | 2 | NA19079.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.89-1996A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749400 | |||||||
| chr8:30749401 | A | AAAAAAT | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0093others(12): Show | 19 | HG01243.hp2 HG01891.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-1992_89-1991ins others(6): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30749401 | ||||||
| chr8:30749401 | A | AAAAAT | 56 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 67 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.89-1992_89-1991ins others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30749401 | ||||||
| chr8:30749405 | T | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(60): Show | 78 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.89-1991T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749405 | |||||||
| chr8:30749410 | T | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02148.hp1 HG02559.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1986T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749410 | |||||||
| chr8:30749608 | CT | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.89-1773delT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30749608 | ||||||
| chr8:30749608 | CTT | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1774_89-1773del others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30749608 | ||||||
| chr8:30749732 | A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(27): Show | 43 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-1664A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749732 | |||||||
| chr8:30749755 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.89-1641G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749755 | |||||||
| chr8:30749760 | C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | NA18984.hp1 NA19001.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.89-1636C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749760 | |||||||
| chr8:30749857 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.89-1539G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749857 | |||||||
| chr8:30749917 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.89-1479T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749917 | |||||||
| chr8:30749922 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.89-1474G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749922 | |||||||
| chr8:30749992 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1404A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30749992 | |||||||
| chr8:30750071 | C | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(115): Show | 134 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.89-1325C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750071 | |||||||
| chr8:30750094 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-1302T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750094 | |||||||
| chr8:30750154 | C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(116): Show | 135 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.89-1242C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750154 | |||||||
| chr8:30750199 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-1197T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750199 | |||||||
| chr8:30750255 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-1141C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750255 | |||||||
| chr8:30750342 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.89-1054C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750342 | |||||||
| chr8:30750388 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-1008T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750388 | |||||||
| chr8:30750508 | C | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0222others(1): Show | 4 | NA18940.hp1 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-888C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750508 | |||||||
| chr8:30750543 | C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01255.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.89-853C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750543 | |||||||
| chr8:30750548 | G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0198 | 2 | HG02300.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.89-848G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750548 | |||||||
| chr8:30750551 | T | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-845T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750551 | |||||||
| chr8:30750559 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.89-837T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750559 | |||||||
| chr8:30750634 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.89-762G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750634 | |||||||
| chr8:30750662 | A | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(165): Show | 184 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.89-734A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750662 | |||||||
| chr8:30750722 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.89-674G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750722 | |||||||
| chr8:30750733 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.89-663A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750733 | |||||||
| chr8:30750763 | ACTCTGTC others(82): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-632_89-544delCT others(87): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750763 | |||||||
| chr8:30750772 | C | CA | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(11): Show | 14 | HG01243.hp2 HG02109.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-612dupA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30750772 | ||||||
| chr8:30750772 | CA | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(118): Show | 137 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.89-612delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30750772 | ||||||
| chr8:30750818 | GA | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 261 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.89-567delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 30750818 | ||||||
| chr8:30750880 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.89-516G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750880 | |||||||
| chr8:30750943 | T | C | 2 | a0001c0001t0003g0046a0001c0001t0003g0047 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.89-453T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30750943 | |||||||
| chr8:30751043 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.89-353C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751043 | |||||||
| chr8:30751059 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.89-337C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751059 | |||||||
| chr8:30751131 | C | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(61): Show | 78 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.89-265C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751131 | |||||||
| chr8:30751141 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.89-255A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751141 | |||||||
| chr8:30751256 | A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 180 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.89-140A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751256 | |||||||
| chr8:30751273 | G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-123G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751273 | |||||||
| chr8:30751332 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.89-64A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751332 | |||||||
| chr8:30751375 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.89-21T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 1/7 | chr8 | 30751375 | |||||||
| chr8:30751534 | A | T | 1 | a0007c0007t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.211+16A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30751534 | |||||||
| chr8:30751544 | T | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 180 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.211+26T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30751544 | |||||||
| chr8:30751561 | A | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 180 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.211+43A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30751561 | |||||||
| chr8:30751894 | C | CT | 15 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0001g0079others(12): Show | 15 | HG01515.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.211+394dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 30751894 | ||||||
| chr8:30751954 | A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG02280.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+436A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30751954 | |||||||
| chr8:30751973 | A | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02155.hp1 HG02273.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+455A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30751973 | |||||||
| chr8:30752142 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.211+624G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752142 | |||||||
| chr8:30752150 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211+632G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752150 | |||||||
| chr8:30752170 | A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.211+652A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752170 | |||||||
| chr8:30752335 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.212-700A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752335 | |||||||
| chr8:30752371 | G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(45): Show | 61 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.212-664G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752371 | |||||||
| chr8:30752489 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.212-546A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752489 | |||||||
| chr8:30752819 | A | G | 2 | a0002c0002t0003g0048a0002c0002t0003g0050 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.212-216A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752819 | |||||||
| chr8:30752825 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.212-210T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30752825 | |||||||
| chr8:30753014 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.212-21T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 2/7 | chr8 | 30753014 | |||||||
| chr8:30753310 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.282+205G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753310 | |||||||
| chr8:30753357 | A | G | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+252A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753357 | |||||||
| chr8:30753404 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.282+299G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753404 | |||||||
| chr8:30753606 | C | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG02280.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.282+501C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753606 | |||||||
| chr8:30753648 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.282+543A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753648 | |||||||
| chr8:30753669 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+564C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753669 | |||||||
| chr8:30753771 | C | CT | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 221 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.282+685dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 30753771 | ||||||
| chr8:30753771 | C | CTT | 30 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 31 | HG00408.hp2 HG02040.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.282+684_282+685dup others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 30753771 | ||||||
| chr8:30753820 | T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(61): Show | 78 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.282+715T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753820 | |||||||
| chr8:30753873 | T | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+768T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30753873 | |||||||
| chr8:30754461 | G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0060 | 2 | NA18957.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.283-204G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30754461 | |||||||
| chr8:30754504 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283-161C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 3/7 | chr8 | 30754504 | |||||||
| chr8:30754836 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.405+49C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30754836 | |||||||
| chr8:30754956 | G | GT | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(61): Show | 78 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.405+185dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 30754956 | ||||||
| chr8:30755025 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.405+238G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755025 | |||||||
| chr8:30755041 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.405+254C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755041 | |||||||
| chr8:30755057 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.405+270G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755057 | |||||||
| chr8:30755064 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.405+277T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755064 | |||||||
| chr8:30755198 | G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.405+411G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755198 | |||||||
| chr8:30755255 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.405+468G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755255 | |||||||
| chr8:30755262 | G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(57): Show | 74 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.405+475G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755262 | |||||||
| chr8:30755491 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.405+704G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755491 | |||||||
| chr8:30755578 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.405+791C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755578 | |||||||
| chr8:30755589 | CA | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.405+812delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 30755589 | ||||||
| chr8:30755722 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.405+935C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755722 | |||||||
| chr8:30755760 | G | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.405+973G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755760 | |||||||
| chr8:30755760 | G | GA | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(118): Show | 138 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.406-984dupA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 30755760 | ||||||
| chr8:30755760 | GA | G | 15 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0088others(12): Show | 15 | HG01243.hp2 HG01256.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.406-984delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 30755760 | ||||||
| chr8:30755927 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.406-838A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30755927 | |||||||
| chr8:30756223 | C | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0027others(20): Show | 24 | HG00621.hp2 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.406-542C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756223 | |||||||
| chr8:30756227 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406-538G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756227 | |||||||
| chr8:30756246 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406-519T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756246 | |||||||
| chr8:30756265 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.406-500C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756265 | |||||||
| chr8:30756353 | C | T | 10 | a0001c0001t0003g0046a0001c0001t0003g0047a0002c0002t0001g0055others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.406-412C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756353 | |||||||
| chr8:30756489 | C | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(115): Show | 134 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.406-276C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756489 | |||||||
| chr8:30756590 | G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG02280.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.406-175G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 4/7 | chr8 | 30756590 | |||||||
| chr8:30757000 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.528+113T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757000 | |||||||
| chr8:30757060 | T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.528+173T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757060 | |||||||
| chr8:30757157 | T | TA | 7 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG01123.hp2 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+285dupA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30757157 | ||||||
| chr8:30757157 | TA | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0121others(5): Show | 8 | HG01168.hp2 HG01256.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+285delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30757157 | ||||||
| chr8:30757278 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+391T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757278 | |||||||
| chr8:30757413 | G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0185 | 2 | NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.528+526G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757413 | |||||||
| chr8:30757530 | C | G | 11 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG02280.hp2 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+643C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757530 | |||||||
| chr8:30757559 | A | T | 11 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG02280.hp2 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+672A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757559 | |||||||
| chr8:30757626 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.528+739C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757626 | |||||||
| chr8:30757642 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.528+755C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757642 | |||||||
| chr8:30757656 | C | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0185 | 2 | NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.528+769C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757656 | |||||||
| chr8:30757854 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.528+967C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757854 | |||||||
| chr8:30757855 | G | A | 5 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+968G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757855 | |||||||
| chr8:30757859 | C | CA | 10 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0140others(7): Show | 10 | HG00735.hp2 HG01358.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.528+990dupA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30757859 | ||||||
| chr8:30757900 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.528+1013T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757900 | |||||||
| chr8:30757953 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+1066C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30757953 | |||||||
| chr8:30758016 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+1129C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758016 | |||||||
| chr8:30758041 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.528+1154G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758041 | |||||||
| chr8:30758046 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.528+1159C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758046 | |||||||
| chr8:30758051 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+1164C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758051 | |||||||
| chr8:30758188 | G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.528+1301G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758188 | |||||||
| chr8:30758431 | A | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG02280.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+1544A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758431 | |||||||
| chr8:30758528 | G | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG00733.hp2 HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.528+1641G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758528 | |||||||
| chr8:30758554 | G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0104 | 3 | NA18954.hp1 NA18973.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.528+1667G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758554 | |||||||
| chr8:30758583 | G | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG02280.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+1696G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758583 | |||||||
| chr8:30758852 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+1965T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758852 | |||||||
| chr8:30758857 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.528+1970T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758857 | |||||||
| chr8:30758870 | ATGTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+1985_528+1996d others(14): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30758870 | ||||||
| chr8:30758872 | G | GT | 5 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0147others(2): Show | 5 | HG00621.hp1 HG01891.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+1993dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30758872 | ||||||
| chr8:30758874 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.528+1987T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758874 | |||||||
| chr8:30758879 | TTGTTTGT others(8): Show |
T | 3 | a0001c0001t0001g0024a0001c0001t0001g0038a0002c0002t0003g0025 | 3 | HG02572.hp2 HG03654.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.528+1994_529-1993d others(17): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30758879 | ||||||
| chr8:30758880 | TG | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(33): Show | 46 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.528+1994delG | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758880 | |||||||
| chr8:30758881 | G | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 211 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.528+1994G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758881 | |||||||
| chr8:30758884 | T | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0082others(13): Show | 19 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.528+1997T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758884 | |||||||
| chr8:30758885 | G | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0082others(15): Show | 21 | HG01109.hp2 HG01175.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.528+1998G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758885 | |||||||
| chr8:30758893 | TG | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.529-1994delG | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758893 | |||||||
| chr8:30758894 | G | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 252 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.529-1994G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758894 | |||||||
| chr8:30758895 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.529-1993T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758895 | |||||||
| chr8:30758900 | T | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(145): Show | 165 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.529-1988T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758900 | |||||||
| chr8:30758900 | T | TG | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG01109.hp1 HG01175.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-1988_529-1987i others(3): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758900 | |||||||
| chr8:30758901 | T | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 9 | HG02280.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1987T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758901 | |||||||
| chr8:30758903 | T | G | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-1985T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758903 | |||||||
| chr8:30758925 | G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(156): Show | 176 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.529-1963G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758925 | |||||||
| chr8:30758954 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.529-1934C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758954 | |||||||
| chr8:30758994 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.529-1894C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758994 | |||||||
| chr8:30758995 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.529-1893G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30758995 | |||||||
| chr8:30759095 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.529-1793G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759095 | |||||||
| chr8:30759100 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.529-1788G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759100 | |||||||
| chr8:30759109 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.529-1779G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759109 | |||||||
| chr8:30759181 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.529-1707C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759181 | |||||||
| chr8:30759204 | A | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0150 | 3 | HG01168.hp1 HG01169.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.529-1684A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759204 | |||||||
| chr8:30759326 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.529-1562C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759326 | |||||||
| chr8:30759345 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-1543C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759345 | |||||||
| chr8:30759465 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.529-1423C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759465 | |||||||
| chr8:30759469 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.529-1419A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759469 | |||||||
| chr8:30759471 | G | A | 1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.529-1417G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759471 | |||||||
| chr8:30759679 | G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(156): Show | 176 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.529-1209G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759679 | |||||||
| chr8:30759717 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-1171G>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759717 | |||||||
| chr8:30759749 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-1139A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759749 | |||||||
| chr8:30759772 | C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(143): Show | 163 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.529-1116C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759772 | |||||||
| chr8:30759819 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.529-1069T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759819 | |||||||
| chr8:30759855 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.529-1033G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759855 | |||||||
| chr8:30759906 | A | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG01243.hp1 HG02145.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.529-982A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759906 | |||||||
| chr8:30759906 | A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 270 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.529-982A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759906 | |||||||
| chr8:30759911 | C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0185 | 2 | NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.529-977C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759911 | |||||||
| chr8:30759926 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.529-962C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759926 | |||||||
| chr8:30759928 | G | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(156): Show | 176 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.529-960G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759928 | |||||||
| chr8:30759950 | C | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0162 | 3 | HG02055.hp1 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.529-938C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30759950 | |||||||
| chr8:30759968 | T | TAAATA | 16 | a0001c0001t0001g0033a0001c0001t0001g0164a0001c0001t0001g0179others(13): Show | 16 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.529-879_529-875dup others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | T | TAAATAAA others(3): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0051 | 3 | HG02055.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.529-884_529-875dup others(10): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | T | TAAATAAA others(8): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0242 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.529-889_529-875dup others(15): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | T | TAAATAAA others(13): Show |
3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02258.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.529-894_529-875dup others(20): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | TAAATA | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0029others(26): Show | 30 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.529-879_529-875del others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | TAAATAAA others(3): Show |
T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0097others(5): Show | 8 | HG01243.hp2 HG01515.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.529-884_529-875del others(10): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | TAAATAAA others(8): Show |
T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(33): Show | 49 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.529-889_529-875del others(15): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30759968 | TAAATAAA others(13): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-894_529-875del others(20): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30759968 | ||||||
| chr8:30760064 | C | CT | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(161): Show | 181 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.529-809dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760064 | ||||||
| chr8:30760064 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-824C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760064 | |||||||
| chr8:30760223 | T | TG | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 271 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.529-664dupG | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760223 | ||||||
| chr8:30760420 | C | CAT | 25 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0140others(22): Show | 28 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.529-445_529-444dup others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760420 | ||||||
| chr8:30760420 | C | CATAT | 6 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0149others(3): Show | 11 | HG00558.hp1 HG00558.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.529-447_529-444dup others(4): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760420 | ||||||
| chr8:30760420 | C | CATATAT | 10 | a0001c0001t0001g0134a0001c0001t0001g0148a0001c0001t0001g0194others(7): Show | 10 | HG01993.hp2 HG02155.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-449_529-444dup others(6): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760420 | ||||||
| chr8:30760435 | A | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.529-453A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760435 | |||||||
| chr8:30760435 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.529-451_529-442del others(10): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760435 | ||||||
| chr8:30760437 | A | ATTT | 3 | a0001c0001t0003g0047a0002c0002t0003g0025a0002c0002t0003g0048 | 3 | HG02258.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-450_529-449ins others(3): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760437 | ||||||
| chr8:30760437 | A | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.529-451A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760437 | |||||||
| chr8:30760439 | A | ATTT | 3 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0050 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.529-448_529-447ins others(3): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760439 | ||||||
| chr8:30760439 | A | T | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.529-449A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760439 | |||||||
| chr8:30760441 | A | ATTTTTT | 6 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-446_529-445ins others(6): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760441 | ||||||
| chr8:30760441 | A | ATTTTTTT | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0119others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-446_529-445ins others(7): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760441 | ||||||
| chr8:30760441 | A | T | 22 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(19): Show | 22 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.529-447A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760441 | |||||||
| chr8:30760442 | TA | T | 3 | a0001c0001t0001g0089a0001c0001t0002g0090a0001c0001t0002g0091 | 3 | HG02257.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.529-445delA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760442 | |||||||
| chr8:30760443 | A | ATAT | 10 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0042others(7): Show | 11 | HG00621.hp2 HG00642.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(3): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATATAT | 13 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00597.hp2 HG02056.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.529-444_529-443ins others(10): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0001g0082 | 4 | HG01978.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(10): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATATTTTT | 7 | a0001c0001t0001g0045a0001c0001t0001g0057a0001c0001t0001g0083others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(7): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATATTTTT others(1): Show |
19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(16): Show | 31 | HG00408.hp2 HG00735.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(8): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATATTTTT others(3): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01255.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.529-444_529-443ins others(10): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATT | 8 | a0001c0001t0001g0141a0001c0001t0001g0146a0001c0001t0001g0178others(5): Show | 8 | HG01168.hp2 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.529-431_529-430dup others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | ATTTTTTT | 6 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 6 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-436_529-430dup others(7): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 30760443 | ||||||
| chr8:30760443 | A | T | 37 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(34): Show | 37 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.529-445A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760443 | |||||||
| chr8:30760444 | T | TA | 5 | a0001c0001t0001g0144a0001c0001t0001g0202a0001c0001t0002g0069others(2): Show | 5 | HG01074.hp2 HG01928.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(1): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760444 | |||||||
| chr8:30760444 | T | TATA | 30 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 33 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(3): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760444 | |||||||
| chr8:30760444 | T | TATATA | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(23): Show | 32 | HG00099.hp2 HG00438.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(5): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760444 | |||||||
| chr8:30760444 | T | TATATATA | 7 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0054others(4): Show | 7 | HG01109.hp1 HG01261.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-444_529-443ins others(7): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760444 | |||||||
| chr8:30760444 | T | TATATATA others(4): Show |
1 | a0001c0001t0004g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.529-444_529-443ins others(11): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760444 | |||||||
| chr8:30760445 | T | A | 10 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0185others(7): Show | 10 | HG02293.hp1 NA18940.hp1 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-443T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760445 | |||||||
| chr8:30760446 | T | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 22 | HG00438.hp2 HG00609.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.529-442T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760446 | |||||||
| chr8:30760447 | T | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0197a0001c0001t0001g0220others(3): Show | 6 | HG02293.hp1 NA18940.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-441T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760447 | |||||||
| chr8:30760448 | T | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0039others(2): Show | 5 | HG03471.hp1 HG03654.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-440T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760448 | |||||||
| chr8:30760504 | C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(45): Show | 61 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.529-384C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760504 | |||||||
| chr8:30760835 | C | T | 1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.529-53C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 5/7 | chr8 | 30760835 | |||||||
| chr8:30761001 | C | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.570+72C>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761001 | |||||||
| chr8:30761049 | T | G | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+120T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761049 | |||||||
| chr8:30761057 | C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+128C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761057 | |||||||
| chr8:30761248 | CT | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0051others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+332delT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 30761248 | ||||||
| chr8:30761326 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+397C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761326 | |||||||
| chr8:30761330 | C | G | 1 | a0001c0001t0002g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.570+401C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761330 | |||||||
| chr8:30761396 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.570+467C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761396 | |||||||
| chr8:30761404 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.570+475C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761404 | |||||||
| chr8:30761405 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.570+476G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761405 | |||||||
| chr8:30761446 | T | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+517T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761446 | |||||||
| chr8:30761509 | C | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(64): Show | 81 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.570+580C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761509 | |||||||
| chr8:30761622 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+693G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761622 | |||||||
| chr8:30761716 | G | GA | 11 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG02280.hp2 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+797dupA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 30761716 | ||||||
| chr8:30761855 | A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(28): Show | 44 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.570+926A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761855 | |||||||
| chr8:30761898 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.570+969A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761898 | |||||||
| chr8:30761932 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+1003A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30761932 | |||||||
| chr8:30762035 | C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0242 | 2 | HG03195.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.570+1106C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762035 | |||||||
| chr8:30762061 | C | CT | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 239 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.570+1149dupT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 30762061 | ||||||
| chr8:30762061 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.570+1132C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762061 | |||||||
| chr8:30762221 | C | T | 7 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG01243.hp2 HG02300.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1052C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762221 | |||||||
| chr8:30762250 | T | A | 2 | a0001c0001t0001g0072a0002c0002t0001g0055 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.571-1023T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762250 | |||||||
| chr8:30762381 | GTTTTTT | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-891_571-886del others(6): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762381 | |||||||
| chr8:30762382 | TTTTTTG | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 196 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.571-866_571-861del others(6): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 30762382 | ||||||
| chr8:30762388 | G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-885G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762388 | |||||||
| chr8:30762773 | A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0065others(12): Show | 16 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-500A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762773 | |||||||
| chr8:30762874 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.571-399G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762874 | |||||||
| chr8:30762876 | CT | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 261 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.571-385delT | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 30762876 | ||||||
| chr8:30762882 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.571-391T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762882 | |||||||
| chr8:30762888 | T | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.571-385T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30762888 | |||||||
| chr8:30763031 | C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0162 | 3 | HG02055.hp1 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.571-242C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30763031 | |||||||
| chr8:30763049 | A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.571-224A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 6/7 | chr8 | 30763049 | |||||||
| chr8:30763415 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.645+68G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30763415 | |||||||
| chr8:30763448 | T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.645+101T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30763448 | |||||||
| chr8:30763616 | A | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 273 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.645+269A>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30763616 | |||||||
| chr8:30763679 | T | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0173 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.645+332T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30763679 | |||||||
| chr8:30763710 | G | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(88): Show | 105 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.645+363G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30763710 | |||||||
| chr8:30763883 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.645+536C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30763883 | |||||||
| chr8:30764060 | C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.645+713C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764060 | |||||||
| chr8:30764116 | A | G | 1 | a0002c0002t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.645+769A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764116 | |||||||
| chr8:30764248 | T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+901T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764248 | |||||||
| chr8:30764307 | G | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0028others(3): Show | 6 | HG02109.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+960G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764307 | |||||||
| chr8:30764325 | C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0082 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.645+978C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764325 | |||||||
| chr8:30764487 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.645+1140A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764487 | |||||||
| chr8:30764541 | T | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.645+1194T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764541 | |||||||
| chr8:30764729 | C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.645+1382C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764729 | |||||||
| chr8:30764773 | C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(175): Show | 196 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.645+1426C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764773 | |||||||
| chr8:30764774 | G | A | 2 | a0001c0001t0003g0046a0001c0001t0003g0047 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.645+1427G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764774 | |||||||
| chr8:30764902 | T | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-1325T>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30764902 | |||||||
| chr8:30765092 | A | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.646-1135A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765092 | |||||||
| chr8:30765093 | A | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.646-1134A>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765093 | |||||||
| chr8:30765097 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.646-1130T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765097 | |||||||
| chr8:30765133 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.646-1094G>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765133 | |||||||
| chr8:30765144 | T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.646-1083T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765144 | |||||||
| chr8:30765234 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.646-993T>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765234 | |||||||
| chr8:30765361 | C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(182): Show | 203 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.646-866C>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765361 | |||||||
| chr8:30765503 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.646-724T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765503 | |||||||
| chr8:30765532 | T | TCA | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(176): Show | 197 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.646-695_646-694ins others(2): Show |
UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765532 | |||||||
| chr8:30765533 | T | C | 6 | a0001c0001t0001g0192a0001c0001t0001g0208a0001c0001t0001g0209others(3): Show | 6 | HG02155.hp1 HG02273.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-694T>C | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765533 | |||||||
| chr8:30765546 | A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0206 | 2 | HG01496.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.646-681A>G | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765546 | |||||||
| chr8:30765639 | C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 62 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.646-588C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765639 | |||||||
| chr8:30765733 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.646-494C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765733 | |||||||
| chr8:30765745 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.646-482C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765745 | |||||||
| chr8:30765766 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-461G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765766 | |||||||
| chr8:30765837 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.646-390G>A | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765837 | |||||||
| chr8:30765915 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.646-312C>T | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | chr8 | 30765915 | |||||||
| chr8:30766010 | C | CA | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(177): Show | 198 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.646-202dupA | UBXN8 | ENSG00000104691.16 | transcript | ENST00000265616.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 30766010 |