Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7322 |
|---|---|
| ensemblid | ENSG00000131508.17 |
| hgncid | 12475 |
| symbol | UBE2D2 |
| name | ubiquitin conjugating enzyme E2 D2 |
| refseq_nuc | NM_003339.3 |
| refseq_prot | NP_003330.1 |
| ensembl_nuc | ENST00000398733.8 |
| ensembl_prot | ENSP00000381717.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 139561339 |
| end | 139628434 |
| strand | + |
| ver | v1.2 |
| region | chr5:139561339-139628434 |
| region5000 | chr5:139556339-139633434 |
| regionname0 | UBE2D2_chr5_139561339_139628434 |
| regionname5000 | UBE2D2_chr5_139556339_139633434 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 147 | 226 | 74 | 46 | 56 | 16 | 32 | 44 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 444 | 226 | 74 | 46 | 56 | 16 | 32 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2087 | 223 | 73 | 45 | 56 | 16 | 31 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| t0002 | 0/0 | 2087 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| t0003 | 0/0 | 2087 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| t0004 | 0/0 | 2087 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0006 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 444 | 226 | 74 | 46 | 56 | 16 | 32 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2530 | 223 | 73 | 45 | 56 | 16 | 31 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| a0001c0001t0002 | 0/0 | 2530 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| a0001c0001t0003 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| a0001c0001t0004 | 0/0 | 2530 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | copy fasta | chr5 | 139556339 | 139633434 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0006 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | USA | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0006 | REF | REF | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0189 | REF | REF | UBE2D2_chr5_139556339_139633434 | UBE2D2 | chr5 | 139556339 | 139633434 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139627018
|
A | C | 1 | a0001c0001t0004 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 7/7 | 217 | chr5 | 139627018 | |||||
| chr5:139627796
|
T | C | 1 | a0001c0001t0002 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 7/7 | 995 | chr5 | 139627796 | |||||
| chr5:139627850
|
T | C | 1 | a0001c0001t0003 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 7/7 | 1049 | chr5 | 139627850 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139562011
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.24+196A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562011 | ||||||
| chr5:139562025
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+210C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562025 | ||||||
| chr5:139562124
|
T | A | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.24+309T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562124 | ||||||
| chr5:139562126
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+311G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562126 | ||||||
| chr5:139562499
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.24+684C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562499 | ||||||
| chr5:139562532
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(4): Show | 7 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+717G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562532 | ||||||
| chr5:139562585
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.24+770A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562585 | ||||||
| chr5:139562764
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+949A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562764 | ||||||
| chr5:139562918
|
C | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+1103C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139562918 | ||||||
| chr5:139563019
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+1204C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139563019 | ||||||
| chr5:139563143
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.24+1328G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139563143 | ||||||
| chr5:139563276
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+1461A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139563276 | ||||||
| chr5:139563478
|
C | CA | 26 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.24+1671dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139563478 | |||||
| chr5:139563540
|
C | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+1725C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139563540 | ||||||
| chr5:139563723
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.24+1908G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139563723 | ||||||
| chr5:139563828
|
T | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.24+2013T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139563828 | ||||||
| chr5:139564008
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+2193A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564008 | ||||||
| chr5:139564105
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(143): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.24+2290T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564105 | ||||||
| chr5:139564195
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | NA18945.hp1 NA18982.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+2380C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564195 | ||||||
| chr5:139564216
|
C | A | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.24+2401C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564216 | ||||||
| chr5:139564476
|
C | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.24+2661C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564476 | ||||||
| chr5:139564476
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+2661C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564476 | ||||||
| chr5:139564699
|
CCA | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+2886_24+2887del others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139564699 | |||||
| chr5:139564848
|
T | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(36): Show | 39 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.24+3033T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564848 | ||||||
| chr5:139564928
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.24+3113T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139564928 | ||||||
| chr5:139565019
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+3204G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565019 | ||||||
| chr5:139565062
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.24+3247C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565062 | ||||||
| chr5:139565100
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.24+3285T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565100 | ||||||
| chr5:139565433
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+3618C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565433 | ||||||
| chr5:139565678
|
T | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.24+3863T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565678 | ||||||
| chr5:139565683
|
T | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.24+3868T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565683 | ||||||
| chr5:139565775
|
G | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+3960G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139565775 | ||||||
| chr5:139566031
|
C | CT | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.24+4231dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139566031 | |||||
| chr5:139566031
|
CT | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0222others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+4231delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139566031 | |||||
| chr5:139566145
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.24+4330A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566145 | ||||||
| chr5:139566377
|
AGGTCATG others(7): Show |
A | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.24+4582_24+4595del others(14): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139566377 | |||||
| chr5:139566397
|
TGCACAGT others(7): Show |
T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+4585_24+4598del others(14): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139566397 | |||||
| chr5:139566403
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.24+4588G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566403 | ||||||
| chr5:139566510
|
C | CA | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0100others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.24+4701dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139566510 | |||||
| chr5:139566549
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.24+4734G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566549 | ||||||
| chr5:139566795
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+4980A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566795 | ||||||
| chr5:139566931
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.24+5116G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566931 | ||||||
| chr5:139566931
|
G | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.24+5116G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566931 | ||||||
| chr5:139566944
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+5129C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139566944 | ||||||
| chr5:139567139
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01167.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.24+5324G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139567139 | ||||||
| chr5:139567168
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+5353C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139567168 | ||||||
| chr5:139567529
|
G | GT | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.24+5736dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139567529 | |||||
| chr5:139567529
|
G | GTT | 16 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 16 | HG01169.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.24+5735_24+5736dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139567529 | |||||
| chr5:139567870
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0087 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.24+6055G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139567870 | ||||||
| chr5:139567993
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.24+6178A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139567993 | ||||||
| chr5:139567996
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24+6181G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139567996 | ||||||
| chr5:139568095
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.24+6280G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139568095 | ||||||
| chr5:139568172
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.24+6357T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139568172 | ||||||
| chr5:139568503
|
C | CA | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+6694dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139568503 | |||||
| chr5:139568688
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.24+6873G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139568688 | ||||||
| chr5:139568755
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+6940G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139568755 | ||||||
| chr5:139568955
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0176 | 2 | HG01175.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.24+7140G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139568955 | ||||||
| chr5:139569256
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+7441G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139569256 | ||||||
| chr5:139569482
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+7667G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139569482 | ||||||
| chr5:139569777
|
G | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(143): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.24+7962G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139569777 | ||||||
| chr5:139569878
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.24+8063T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139569878 | ||||||
| chr5:139569881
|
G | T | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.24+8066G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139569881 | ||||||
| chr5:139569975
|
A | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG03209.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.24+8160A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139569975 | ||||||
| chr5:139570007
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.24+8192C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570007 | ||||||
| chr5:139570020
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.24+8205C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570020 | ||||||
| chr5:139570046
|
A | G | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG01993.hp1 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+8231A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570046 | ||||||
| chr5:139570099
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG01167.hp2 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+8284G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570099 | ||||||
| chr5:139570145
|
TAGTCCTA others(10): Show |
T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+8333_24+8349del others(17): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139570145 | |||||
| chr5:139570229
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.24+8414C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570229 | ||||||
| chr5:139570293
|
A | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01069.hp1 HG01071.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.24+8478A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570293 | ||||||
| chr5:139570351
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0088 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.24+8536T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570351 | ||||||
| chr5:139570501
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.24+8686C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570501 | ||||||
| chr5:139570715
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.24+8900G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570715 | ||||||
| chr5:139570746
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.24+8931C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570746 | ||||||
| chr5:139570943
|
AC | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0187 | 2 | NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.24+9129delC | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139570943 | ||||||
| chr5:139571080
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.24+9265C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571080 | ||||||
| chr5:139571092
|
T | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+9277T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571092 | ||||||
| chr5:139571406
|
C | CA | 7 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0038others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+9608dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139571406 | |||||
| chr5:139571406
|
CA | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0213others(2): Show | 5 | HG01496.hp2 HG01515.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+9608delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139571406 | |||||
| chr5:139571429
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.24+9614A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571429 | ||||||
| chr5:139571627
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+9812G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571627 | ||||||
| chr5:139571648
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+9833A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571648 | ||||||
| chr5:139571704
|
A | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.24+9889A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571704 | ||||||
| chr5:139571793
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(90): Show | 94 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.24+9978C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571793 | ||||||
| chr5:139571807
|
CTCCT | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0077others(1): Show | 4 | HG02132.hp2 NA18973.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+10002_24+10005d others(6): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139571807 | |||||
| chr5:139571844
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0090 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.24+10029C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571844 | ||||||
| chr5:139571929
|
TA | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 7 | HG01993.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+10127delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139571929 | |||||
| chr5:139571976
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.24+10161A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139571976 | ||||||
| chr5:139572287
|
A | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+10472A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139572287 | ||||||
| chr5:139572294
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.24+10479C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139572294 | ||||||
| chr5:139572396
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+10581C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139572396 | ||||||
| chr5:139572399
|
T | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00741.hp1 HG01167.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+10584T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139572399 | ||||||
| chr5:139572647
|
CT | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+10848delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139572647 | |||||
| chr5:139572891
|
G | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+11076G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139572891 | ||||||
| chr5:139572981
|
TA | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+11168delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139572981 | |||||
| chr5:139572988
|
A | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(1): Show | 4 | HG02135.hp2 HG03927.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+11173A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139572988 | ||||||
| chr5:139573146
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.24+11331A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139573146 | ||||||
| chr5:139573162
|
CGTG | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0031others(2): Show | 5 | HG02486.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+11355_24+11357d others(5): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139573162 | |||||
| chr5:139573229
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+11414G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139573229 | ||||||
| chr5:139573656
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.24+11841G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139573656 | ||||||
| chr5:139573751
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.24+11936C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139573751 | ||||||
| chr5:139573956
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.24+12141G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139573956 | ||||||
| chr5:139574004
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(142): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.24+12189C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139574004 | ||||||
| chr5:139574111
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.24+12296G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139574111 | ||||||
| chr5:139574117
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.24+12302G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139574117 | ||||||
| chr5:139574280
|
CA | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0037others(7): Show | 10 | HG02622.hp1 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.24+12481delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139574280 | |||||
| chr5:139574388
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.24+12573G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139574388 | ||||||
| chr5:139574711
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.24+12896G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139574711 | ||||||
| chr5:139574735
|
CA | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG01168.hp2 HG01496.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+12938delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139574735 | |||||
| chr5:139574735
|
CAA | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0197others(24): Show | 27 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.24+12937_24+12938d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139574735 | |||||
| chr5:139574972
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0004g0192 | 3 | HG00741.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.24+13157G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139574972 | ||||||
| chr5:139575418
|
TTCA | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+13606_24+13608d others(5): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139575418 | |||||
| chr5:139575426
|
C | CACCCCAA others(26): Show |
1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.24+13613_24+13645d others(35): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139575426 | |||||
| chr5:139575720
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.24+13905A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139575720 | ||||||
| chr5:139576144
|
C | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0062others(15): Show | 18 | HG01175.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.24+14329C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576144 | ||||||
| chr5:139576201
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.24+14386C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576201 | ||||||
| chr5:139576283
|
A | G | 18 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0062others(15): Show | 18 | HG01175.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.24+14468A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576283 | ||||||
| chr5:139576430
|
TG | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+14616delG | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576430 | ||||||
| chr5:139576432
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+14617T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576432 | ||||||
| chr5:139576512
|
A | G | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(7): Show | 10 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.24+14697A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576512 | ||||||
| chr5:139576556
|
A | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+14741A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576556 | ||||||
| chr5:139576656
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.24+14841T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576656 | ||||||
| chr5:139576658
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.24+14843C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576658 | ||||||
| chr5:139576894
|
T | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG01099.hp1 HG01167.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+15079T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139576894 | ||||||
| chr5:139576943
|
C | CT | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.24+15144dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139576943 | |||||
| chr5:139576943
|
C | CTT | 21 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0063others(18): Show | 21 | HG01175.hp1 HG01257.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.24+15143_24+15144d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139576943 | |||||
| chr5:139576967
|
A | AT | 10 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0079others(7): Show | 10 | HG01070.hp2 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.24+15169dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139576967 | |||||
| chr5:139576967
|
AT | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.24+15169delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139576967 | |||||
| chr5:139576967
|
ATT | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0018others(28): Show | 31 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.24+15168_24+15169d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139576967 | |||||
| chr5:139577048
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.24+15233A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139577048 | ||||||
| chr5:139577179
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0001g0091 | 3 | HG01192.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.24+15364C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139577179 | ||||||
| chr5:139577404
|
C | CT | 27 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(24): Show | 28 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.24+15614dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139577404 | |||||
| chr5:139577404
|
CT | C | 47 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(44): Show | 47 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.24+15614delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139577404 | |||||
| chr5:139577477
|
GA | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+15663delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139577477 | ||||||
| chr5:139577507
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.24+15692G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139577507 | ||||||
| chr5:139577754
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.24+15939C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139577754 | ||||||
| chr5:139577858
|
T | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+16043T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139577858 | ||||||
| chr5:139578434
|
T | TTG | 33 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0041others(30): Show | 33 | HG00323.hp2 HG01099.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.24+16653_24+16654d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139578434 | |||||
| chr5:139578434
|
T | TTGTG | 6 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0045others(3): Show | 6 | HG01167.hp2 HG01884.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.24+16651_24+16654d others(6): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139578434 | |||||
| chr5:139578434
|
TTG | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 42 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.24+16653_24+16654d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139578434 | |||||
| chr5:139578434
|
TTGTG | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(21): Show | 24 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.24+16651_24+16654d others(6): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139578434 | |||||
| chr5:139578493
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.24+16678T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139578493 | ||||||
| chr5:139578576
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.24+16761T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139578576 | ||||||
| chr5:139578738
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.24+16923C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139578738 | ||||||
| chr5:139578912
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+17097A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139578912 | ||||||
| chr5:139579002
|
C | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+17187C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139579002 | ||||||
| chr5:139579010
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+17195C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139579010 | ||||||
| chr5:139579030
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0092 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.24+17215C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139579030 | ||||||
| chr5:139579241
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+17426C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139579241 | ||||||
| chr5:139579396
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.24+17581C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139579396 | ||||||
| chr5:139580045
|
C | CAAAA | 7 | a0001c0001t0001g0197a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG00741.hp1 HG01167.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+18243_24+18246d others(6): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139580045 | |||||
| chr5:139580045
|
C | CAAAAA | 23 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(20): Show | 23 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.24+18242_24+18246d others(7): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139580045 | |||||
| chr5:139580059
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.24+18244A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139580059 | ||||||
| chr5:139580317
|
A | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+18502A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139580317 | ||||||
| chr5:139580395
|
T | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.24+18580T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139580395 | ||||||
| chr5:139580418
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.24+18603T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139580418 | ||||||
| chr5:139580451
|
C | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0171others(1): Show | 4 | NA18946.hp1 NA18987.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+18636C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139580451 | ||||||
| chr5:139581061
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.24+19246G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581061 | ||||||
| chr5:139581077
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.24+19262G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581077 | ||||||
| chr5:139581509
|
C | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-18863C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581509 | ||||||
| chr5:139581674
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25-18698T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581674 | ||||||
| chr5:139581705
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.25-18667G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581705 | ||||||
| chr5:139581731
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0095 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.25-18641C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581731 | ||||||
| chr5:139581809
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.25-18563C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581809 | ||||||
| chr5:139581986
|
T | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.25-18386T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139581986 | ||||||
| chr5:139582266
|
A | AT | 35 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(32): Show | 35 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.25-18092dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139582266 | |||||
| chr5:139582666
|
A | AT | 30 | a0001c0001t0001g0017a0001c0001t0001g0129a0001c0001t0001g0137others(27): Show | 30 | HG00280.hp1 HG00741.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.25-17684dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139582666 | |||||
| chr5:139582666
|
AT | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0019others(94): Show | 98 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.25-17684delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139582666 | |||||
| chr5:139582666
|
ATT | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-17685_25-17684d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139582666 | |||||
| chr5:139582823
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.25-17549G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139582823 | ||||||
| chr5:139582965
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25-17407C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139582965 | ||||||
| chr5:139582969
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-17403T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139582969 | ||||||
| chr5:139582977
|
CT | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0041others(36): Show | 39 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.25-17381delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139582977 | |||||
| chr5:139583000
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-17372C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583000 | ||||||
| chr5:139583002
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25-17370T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583002 | ||||||
| chr5:139583005
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25-17367C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583005 | ||||||
| chr5:139583034
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25-17338G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583034 | ||||||
| chr5:139583036
|
A | C | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25-17336A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583036 | ||||||
| chr5:139583096
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25-17276T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583096 | ||||||
| chr5:139583097
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25-17275C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583097 | ||||||
| chr5:139583117
|
G | T | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25-17255G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583117 | ||||||
| chr5:139583458
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.25-16914A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583458 | ||||||
| chr5:139583932
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25-16440C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139583932 | ||||||
| chr5:139584393
|
T | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-15979T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584393 | ||||||
| chr5:139584461
|
C | CAAAT | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.25-15908_25-15907i others(6): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139584461 | |||||
| chr5:139584533
|
C | CTT | 98 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 99 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.25-15825_25-15824d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139584533 | |||||
| chr5:139584533
|
C | CTTT | 7 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0088others(4): Show | 7 | HG00741.hp1 HG01167.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-15826_25-15824d others(5): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139584533 | |||||
| chr5:139584533
|
C | CTTTTT | 24 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(21): Show | 24 | HG00280.hp1 HG00597.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.25-15828_25-15824d others(7): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139584533 | |||||
| chr5:139584562
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-15810C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584562 | ||||||
| chr5:139584563
|
G | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0043others(4): Show | 7 | HG02129.hp1 HG02132.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-15809G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584563 | ||||||
| chr5:139584572
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.25-15800G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584572 | ||||||
| chr5:139584586
|
G | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02622.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.25-15786G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584586 | ||||||
| chr5:139584662
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-15710A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584662 | ||||||
| chr5:139584725
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.25-15647G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584725 | ||||||
| chr5:139584754
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0183 | 3 | HG01168.hp2 HG01169.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.25-15618A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584754 | ||||||
| chr5:139584849
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25-15523T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139584849 | ||||||
| chr5:139584901
|
C | CT | 5 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0046others(2): Show | 5 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-15455dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139584901 | |||||
| chr5:139585057
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01069.hp1 HG01071.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.25-15315C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139585057 | ||||||
| chr5:139585067
|
AT | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-15301delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139585067 | |||||
| chr5:139585100
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0164 | 2 | HG02135.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.25-15272A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139585100 | ||||||
| chr5:139585210
|
CT | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0107others(37): Show | 40 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.25-15146delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139585210 | |||||
| chr5:139585231
|
CAG | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.25-15138_25-15137d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139585231 | |||||
| chr5:139585351
|
T | G | 1 | a0001c0001t0001g0137 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.25-15021T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139585351 | ||||||
| chr5:139585791
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.25-14581A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139585791 | ||||||
| chr5:139585935
|
C | CA | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0024others(54): Show | 57 | HG00280.hp1 HG00597.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.25-14411dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139585935 | |||||
| chr5:139585935
|
C | CAA | 7 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0199others(4): Show | 7 | HG00323.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-14412_25-14411d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139585935 | |||||
| chr5:139585935
|
CA | C | 25 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0035others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.25-14411delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139585935 | |||||
| chr5:139586101
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-14271A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139586101 | ||||||
| chr5:139586403
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.25-13969T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139586403 | ||||||
| chr5:139586546
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.25-13826A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139586546 | ||||||
| chr5:139586737
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25-13635C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139586737 | ||||||
| chr5:139586839
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.25-13533C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139586839 | ||||||
| chr5:139587244
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-13128A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587244 | ||||||
| chr5:139587270
|
C | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-13102C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587270 | ||||||
| chr5:139587306
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.25-13066G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587306 | ||||||
| chr5:139587323
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25-13049C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587323 | ||||||
| chr5:139587327
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.25-13045G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587327 | ||||||
| chr5:139587364
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.25-13008G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587364 | ||||||
| chr5:139587540
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.25-12832G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587540 | ||||||
| chr5:139587602
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.25-12770G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587602 | ||||||
| chr5:139587672
|
C | CA | 67 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.25-12678dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139587672 | |||||
| chr5:139587672
|
C | CAA | 5 | a0001c0001t0001g0126a0001c0001t0001g0200a0001c0001t0001g0205others(2): Show | 5 | HG00741.hp1 HG03710.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-12679_25-12678d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139587672 | |||||
| chr5:139587672
|
CA | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0073others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-12678delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139587672 | |||||
| chr5:139587697
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0088a0001c0001t0001g0096others(2): Show | 5 | HG02622.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-12675G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587697 | ||||||
| chr5:139587723
|
TAATAGAG others(3): Show |
T | 1 | a0001c0001t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25-12636_25-12627d others(12): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139587723 | |||||
| chr5:139587923
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.25-12449C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587923 | ||||||
| chr5:139587940
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.25-12432G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139587940 | ||||||
| chr5:139588248
|
G | GT | 8 | a0001c0001t0001g0079a0001c0001t0001g0100a0001c0001t0001g0105others(5): Show | 8 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-12113dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139588248 | |||||
| chr5:139588255
|
T | G | 33 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0128others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.25-12117T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588255 | ||||||
| chr5:139588275
|
G | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00741.hp1 HG01167.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-12097G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588275 | ||||||
| chr5:139588349
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.25-12023C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588349 | ||||||
| chr5:139588362
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0177 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.25-12010G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588362 | ||||||
| chr5:139588414
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.25-11958T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588414 | ||||||
| chr5:139588784
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.25-11588T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588784 | ||||||
| chr5:139588859
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25-11513C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139588859 | ||||||
| chr5:139589052
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25-11320A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589052 | ||||||
| chr5:139589169
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG02622.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.25-11203G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589169 | ||||||
| chr5:139589252
|
CTG | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-11118_25-11117d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139589252 | |||||
| chr5:139589402
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-10970G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589402 | ||||||
| chr5:139589594
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(90): Show | 94 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.25-10778G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589594 | ||||||
| chr5:139589877
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-10495T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589877 | ||||||
| chr5:139589886
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-10486A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589886 | ||||||
| chr5:139589946
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25-10426G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139589946 | ||||||
| chr5:139590149
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.25-10223G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590149 | ||||||
| chr5:139590443
|
T | TA | 8 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-9915dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590443 | |||||
| chr5:139590443
|
TA | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-9915delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590443 | |||||
| chr5:139590518
|
T | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0043others(5): Show | 8 | HG02129.hp1 HG02132.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-9854T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590518 | ||||||
| chr5:139590531
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-9841A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590531 | ||||||
| chr5:139590715
|
A | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-9657A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590715 | ||||||
| chr5:139590741
|
C | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.25-9631C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590741 | ||||||
| chr5:139590782
|
C | CT | 44 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.25-9560dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
C | CTT | 10 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0086others(7): Show | 10 | HG01346.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-9561_25-9560dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0001t0001g0214 | 3 | HG00597.hp2 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.25-9569_25-9560dup others(10): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG03239.hp1 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.25-9570_25-9560dup others(11): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.25-9571_25-9560dup others(12): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25-9577_25-9560dup others(18): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0209 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.25-9578_25-9560dup others(19): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
CT | C | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(14): Show | 17 | HG00639.hp2 HG01070.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.25-9560delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0164 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.25-9569_25-9560del others(10): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0077a0001c0001t0004g0192 | 2 | HG00741.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.25-9570_25-9560del others(11): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0127 | 3 | HG03471.hp1 HG03516.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.25-9571_25-9560del others(12): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.25-9572_25-9560del others(13): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590782
|
CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0003a0001c0001t0001g0196a0001c0001t0001g0201others(4): Show | 7 | HG02523.hp2 HG02602.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-9576_25-9560del others(17): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139590782 | |||||
| chr5:139590786
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-9586T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590786 | ||||||
| chr5:139590789
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.25-9583T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590789 | ||||||
| chr5:139590840
|
G | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG02622.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.25-9532G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139590840 | ||||||
| chr5:139591021
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.25-9351T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139591021 | ||||||
| chr5:139591205
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-9167G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139591205 | ||||||
| chr5:139591288
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-9084C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139591288 | ||||||
| chr5:139591415
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.25-8957T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139591415 | ||||||
| chr5:139591540
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.25-8832A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139591540 | ||||||
| chr5:139591560
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.25-8812G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139591560 | ||||||
| chr5:139592158
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-8214C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139592158 | ||||||
| chr5:139592248
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0058 | 2 | HG01257.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.25-8124G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139592248 | ||||||
| chr5:139592259
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-8113C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139592259 | ||||||
| chr5:139592596
|
C | CT | 7 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0079others(4): Show | 7 | HG01175.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-7754dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139592596 | |||||
| chr5:139592596
|
CT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.25-7754delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139592596 | |||||
| chr5:139592727
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.25-7645C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139592727 | ||||||
| chr5:139592759
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.25-7613T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139592759 | ||||||
| chr5:139592965
|
AT | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.25-7405delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139592965 | |||||
| chr5:139592996
|
C | CT | 47 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0022others(44): Show | 47 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.25-7359dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139592996 | |||||
| chr5:139593015
|
A | T | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.25-7357A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593015 | ||||||
| chr5:139593048
|
T | G | 1 | a0001c0001t0002g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.25-7324T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593048 | ||||||
| chr5:139593065
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.25-7307G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593065 | ||||||
| chr5:139593462
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25-6910T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593462 | ||||||
| chr5:139593475
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25-6897C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593475 | ||||||
| chr5:139593496
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(66): Show | 70 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.25-6876A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593496 | ||||||
| chr5:139593499
|
T | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-6873T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593499 | ||||||
| chr5:139593517
|
GTATACAT others(7): Show |
G | 1 | a0001c0001t0001g0054 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.25-6836_25-6823del others(14): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139593517 | |||||
| chr5:139593650
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.25-6722C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593650 | ||||||
| chr5:139593759
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.25-6613T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593759 | ||||||
| chr5:139593890
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.25-6482A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593890 | ||||||
| chr5:139593992
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.25-6380G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139593992 | ||||||
| chr5:139594122
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.25-6250G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139594122 | ||||||
| chr5:139594351
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25-6021A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139594351 | ||||||
| chr5:139594574
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-5798C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139594574 | ||||||
| chr5:139594580
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-5792A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139594580 | ||||||
| chr5:139595239
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.25-5133G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595239 | ||||||
| chr5:139595300
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.25-5072G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595300 | ||||||
| chr5:139595309
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.25-5063T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595309 | ||||||
| chr5:139595380
|
G | GT | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01099.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-4981dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139595380 | |||||
| chr5:139595525
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-4847C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595525 | ||||||
| chr5:139595656
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01167.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25-4716A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595656 | ||||||
| chr5:139595859
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.25-4513A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595859 | ||||||
| chr5:139595890
|
TTG | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG03225.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-4480_25-4479del others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139595890 | |||||
| chr5:139595891
|
TG | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0218 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.25-4480delG | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595891 | ||||||
| chr5:139595892
|
G | GT | 10 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0130others(7): Show | 10 | HG00597.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.25-4461dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139595892 | |||||
| chr5:139595892
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0115 | 2 | HG02165.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.25-4480G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595892 | ||||||
| chr5:139595892
|
GT | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(92): Show | 96 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.25-4461delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139595892 | |||||
| chr5:139595892
|
GTT | G | 22 | a0001c0001t0001g0101a0001c0001t0001g0194a0001c0001t0001g0195others(19): Show | 22 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.25-4462_25-4461del others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139595892 | |||||
| chr5:139595896
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-4476T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595896 | ||||||
| chr5:139595936
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-4436C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595936 | ||||||
| chr5:139595952
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25-4420G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139595952 | ||||||
| chr5:139596128
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25-4244A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139596128 | ||||||
| chr5:139596538
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25-3834C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139596538 | ||||||
| chr5:139596742
|
A | AAAT | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-3610_25-3608dup others(3): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139596742 | |||||
| chr5:139596774
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-3598C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139596774 | ||||||
| chr5:139596915
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.25-3457T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139596915 | ||||||
| chr5:139596978
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0092 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.25-3394C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139596978 | ||||||
| chr5:139597002
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-3370G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139597002 | ||||||
| chr5:139597061
|
T | TAAAAAAA others(321): Show |
1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25-3295_25-3294ins others(328): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139597061 | |||||
| chr5:139597067
|
A | AAATAATA others(353): Show |
1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.25-3295_25-3294ins others(360): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139597067 | |||||
| chr5:139597067
|
A | AAATAATA others(348): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.25-3295_25-3294ins others(355): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139597067 | |||||
| chr5:139597596
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0053 | 3 | HG00733.hp2 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.25-2776A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139597596 | ||||||
| chr5:139597795
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.25-2577T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139597795 | ||||||
| chr5:139598026
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.25-2346C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139598026 | ||||||
| chr5:139598075
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25-2297A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139598075 | ||||||
| chr5:139598278
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-2094G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139598278 | ||||||
| chr5:139598552
|
C | CT | 55 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0025others(52): Show | 55 | HG00280.hp1 HG01167.hp2 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.25-1794dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598552 | |||||
| chr5:139598552
|
C | CTT | 10 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0200others(7): Show | 10 | HG00597.hp2 HG02055.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-1795_25-1794dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598552 | |||||
| chr5:139598552
|
CT | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0121others(2): Show | 5 | HG00741.hp1 HG01168.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-1794delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598552 | |||||
| chr5:139598914
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25-1458T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139598914 | ||||||
| chr5:139598919
|
C | CT | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0137others(26): Show | 29 | HG00280.hp1 HG00597.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.25-1427dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598919 | |||||
| chr5:139598919
|
C | CTT | 5 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0213others(2): Show | 5 | HG00597.hp2 HG01496.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-1428_25-1427dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598919 | |||||
| chr5:139598919
|
CT | C | 54 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0023others(51): Show | 54 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.25-1427delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598919 | |||||
| chr5:139598919
|
CTT | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(58): Show | 62 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.25-1428_25-1427del others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139598919 | |||||
| chr5:139599512
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.25-860G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599512 | ||||||
| chr5:139599596
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25-776C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599596 | ||||||
| chr5:139599629
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.25-743C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599629 | ||||||
| chr5:139599683
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.25-689G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599683 | ||||||
| chr5:139599739
|
A | AAAACAAA others(4): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.25-622_25-612dupCA others(9): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139599739 | |||||
| chr5:139599979
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-393A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599979 | ||||||
| chr5:139599982
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25-390T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599982 | ||||||
| chr5:139599986
|
G | C | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-386G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | chr5 | 139599986 | ||||||
| chr5:139600283
|
CAG | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25-85_25-84delGA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 139600283 | |||||
| chr5:139600462
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+27T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139600462 | ||||||
| chr5:139600789
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.88+354C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139600789 | ||||||
| chr5:139600800
|
CTTTA | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+373_88+376delAT others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139600800 | |||||
| chr5:139600826
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0157a0001c0001t0001g0181 | 3 | HG01934.hp2 HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.88+391G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139600826 | ||||||
| chr5:139601050
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.88+615G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139601050 | ||||||
| chr5:139601401
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.88+966C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139601401 | ||||||
| chr5:139601457
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.88+1022A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139601457 | ||||||
| chr5:139601658
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+1223C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139601658 | ||||||
| chr5:139601676
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0183 | 3 | HG01168.hp2 HG01169.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.88+1241C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139601676 | ||||||
| chr5:139602088
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+1653G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139602088 | ||||||
| chr5:139602953
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | NA18945.hp1 NA18982.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+2518G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139602953 | ||||||
| chr5:139603383
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+2948A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139603383 | ||||||
| chr5:139603484
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+3049G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139603484 | ||||||
| chr5:139603554
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.88+3119G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139603554 | ||||||
| chr5:139603584
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.88+3149T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139603584 | ||||||
| chr5:139603615
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+3180C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139603615 | ||||||
| chr5:139603623
|
G | GA | 10 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0075others(7): Show | 10 | HG00597.hp1 HG00741.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+3211dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139603623 | |||||
| chr5:139603623
|
G | GAA | 23 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(20): Show | 23 | HG00280.hp1 HG00597.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.88+3210_88+3211dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139603623 | |||||
| chr5:139603623
|
G | GAAA | 7 | a0001c0001t0001g0203a0001c0001t0001g0211a0001c0001t0001g0217others(4): Show | 7 | HG00741.hp1 HG01167.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+3209_88+3211dup others(3): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139603623 | |||||
| chr5:139603623
|
GA | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(51): Show | 55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.88+3211delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139603623 | |||||
| chr5:139603849
|
TGAGGCAG others(25): Show |
T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | NA18945.hp1 NA18982.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+3420_88+3451del others(32): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139603849 | |||||
| chr5:139604140
|
C | CT | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(7): Show | 10 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+3722dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139604140 | |||||
| chr5:139604465
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.88+4030A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139604465 | ||||||
| chr5:139604819
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.88+4384G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139604819 | ||||||
| chr5:139604880
|
T | TA | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.88+4461dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139604880 | |||||
| chr5:139604880
|
TA | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.88+4461delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139604880 | |||||
| chr5:139605314
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88+4879C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139605314 | ||||||
| chr5:139605361
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+4926G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139605361 | ||||||
| chr5:139605367
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.88+4932C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139605367 | ||||||
| chr5:139605591
|
C | CA | 11 | a0001c0001t0001g0135a0001c0001t0001g0172a0001c0001t0001g0182others(8): Show | 11 | HG00741.hp1 HG01106.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+5179dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139605591 | |||||
| chr5:139605591
|
C | CAA | 5 | a0001c0001t0001g0066a0001c0001t0001g0200a0001c0001t0001g0202others(2): Show | 5 | HG00597.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+5178_88+5179dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139605591 | |||||
| chr5:139605591
|
CA | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(90): Show | 94 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.88+5179delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139605591 | |||||
| chr5:139605610
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88+5175A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139605610 | ||||||
| chr5:139605669
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.88+5234C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139605669 | ||||||
| chr5:139605737
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.88+5302C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139605737 | ||||||
| chr5:139605910
|
T | TA | 28 | a0001c0001t0001g0003a0001c0001t0001g0166a0001c0001t0001g0194others(25): Show | 28 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.88+5486dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139605910 | |||||
| chr5:139606017
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+5582G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139606017 | ||||||
| chr5:139606032
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+5597C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139606032 | ||||||
| chr5:139606109
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.88+5674T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139606109 | ||||||
| chr5:139606203
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+5768C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139606203 | ||||||
| chr5:139606309
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.88+5874G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139606309 | ||||||
| chr5:139606396
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.88+5961C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139606396 | ||||||
| chr5:139607052
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+6617C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139607052 | ||||||
| chr5:139607084
|
G | A | 22 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0034others(19): Show | 22 | HG00733.hp2 HG01070.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.88+6649G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139607084 | ||||||
| chr5:139607662
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.89-6924T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139607662 | ||||||
| chr5:139607707
|
A | G | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-6879A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139607707 | ||||||
| chr5:139608017
|
G | GA | 7 | a0001c0001t0001g0035a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG01175.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-6554dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139608017 | |||||
| chr5:139608169
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.89-6417C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608169 | ||||||
| chr5:139608171
|
G | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(143): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.89-6415G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608171 | ||||||
| chr5:139608295
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.89-6291A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608295 | ||||||
| chr5:139608363
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG03209.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.89-6223G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608363 | ||||||
| chr5:139608444
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-6142A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608444 | ||||||
| chr5:139608594
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.89-5992T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608594 | ||||||
| chr5:139608634
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.89-5952T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608634 | ||||||
| chr5:139608693
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.89-5893C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608693 | ||||||
| chr5:139608807
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.89-5779G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608807 | ||||||
| chr5:139608883
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.89-5703G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139608883 | ||||||
| chr5:139609031
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.89-5555G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609031 | ||||||
| chr5:139609086
|
C | CA | 12 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0067others(9): Show | 12 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-5487dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139609086 | |||||
| chr5:139609119
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.89-5467A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609119 | ||||||
| chr5:139609331
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.89-5255C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609331 | ||||||
| chr5:139609376
|
C | CT | 21 | a0001c0001t0001g0003a0001c0001t0001g0196a0001c0001t0001g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-5199dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139609376 | |||||
| chr5:139609376
|
C | CTT | 5 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(2): Show | 5 | HG00280.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-5200_89-5199dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139609376 | |||||
| chr5:139609400
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.89-5186C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609400 | ||||||
| chr5:139609401
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-5185G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609401 | ||||||
| chr5:139609660
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.89-4926C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609660 | ||||||
| chr5:139609684
|
TA | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0051a0001c0001t0001g0174others(3): Show | 6 | HG01167.hp1 HG01255.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-4887delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139609684 | |||||
| chr5:139609699
|
A | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG01993.hp1 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-4887A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609699 | ||||||
| chr5:139609726
|
C | CT | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-4853dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139609726 | |||||
| chr5:139609875
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4711G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139609875 | ||||||
| chr5:139610264
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4322C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610264 | ||||||
| chr5:139610278
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.89-4308C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610278 | ||||||
| chr5:139610546
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.89-4040A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610546 | ||||||
| chr5:139610548
|
A | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0018others(63): Show | 67 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.89-4038A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610548 | ||||||
| chr5:139610555
|
T | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(68): Show | 72 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.89-4031T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610555 | ||||||
| chr5:139610557
|
T | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0118 | 2 | HG02895.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.89-4029T>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610557 | ||||||
| chr5:139610688
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.89-3898C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610688 | ||||||
| chr5:139610702
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-3884G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610702 | ||||||
| chr5:139610995
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0053 | 3 | HG00733.hp2 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.89-3591C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139610995 | ||||||
| chr5:139611005
|
C | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3581C>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139611005 | ||||||
| chr5:139611120
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.89-3466C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139611120 | ||||||
| chr5:139611175
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0001g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.89-3383_89-3382ins others(38): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611175 | |||||
| chr5:139611175
|
CT | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.89-3383delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611175 | |||||
| chr5:139611175
|
CTT | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0061others(6): Show | 9 | HG01069.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-3384_89-3383del others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611175 | |||||
| chr5:139611175
|
CTTTTTTT others(2): Show |
C | 27 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0197others(24): Show | 27 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.89-3391_89-3383del others(9): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611175 | |||||
| chr5:139611175
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.89-3393_89-3383del others(11): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611175 | |||||
| chr5:139611278
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.89-3308C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139611278 | ||||||
| chr5:139611420
|
T | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-3166T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139611420 | ||||||
| chr5:139611824
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-2762A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139611824 | ||||||
| chr5:139611858
|
CCT | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2727_89-2726del others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139611858 | ||||||
| chr5:139611961
|
G | GT | 30 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 30 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.89-2607dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611961 | |||||
| chr5:139611961
|
G | GTT | 12 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0196others(9): Show | 12 | HG00741.hp1 HG02486.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-2608_89-2607dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611961 | |||||
| chr5:139611961
|
GT | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0029others(9): Show | 13 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.89-2607delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139611961 | |||||
| chr5:139612090
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.89-2496G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139612090 | ||||||
| chr5:139612712
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.89-1874C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139612712 | ||||||
| chr5:139612762
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-1824G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139612762 | ||||||
| chr5:139613046
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00741.hp1 HG01167.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-1540A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613046 | ||||||
| chr5:139613118
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(67): Show | 71 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.89-1468A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613118 | ||||||
| chr5:139613214
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-1372G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613214 | ||||||
| chr5:139613267
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.89-1319G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613267 | ||||||
| chr5:139613577
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.89-1009T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613577 | ||||||
| chr5:139613626
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-960T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613626 | ||||||
| chr5:139613830
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.89-756T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613830 | ||||||
| chr5:139613980
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-606T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139613980 | ||||||
| chr5:139614022
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-564A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139614022 | ||||||
| chr5:139614061
|
CA | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.89-505delA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139614061 | |||||
| chr5:139614061
|
CAA | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0222others(2): Show | 5 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-506_89-505delAA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139614061 | |||||
| chr5:139614061
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-516_89-505delAA others(10): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 139614061 | |||||
| chr5:139614339
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.89-247G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 2/6 | chr5 | 139614339 | ||||||
| chr5:139615003
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.304+37G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615003 | ||||||
| chr5:139615027
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.304+61T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615027 | ||||||
| chr5:139615112
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.304+146C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615112 | ||||||
| chr5:139615193
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0078 | 2 | NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.304+227A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615193 | ||||||
| chr5:139615222
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.304+256T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615222 | ||||||
| chr5:139615353
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.304+387C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615353 | ||||||
| chr5:139615396
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304+430A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615396 | ||||||
| chr5:139615479
|
T | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.304+513T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615479 | ||||||
| chr5:139615738
|
T | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0061others(1): Show | 4 | HG01192.hp2 HG01255.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+772T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139615738 | ||||||
| chr5:139615829
|
A | AT | 38 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(35): Show | 39 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.304+887dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139615829 | |||||
| chr5:139615829
|
A | ATT | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0037others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.304+886_304+887dup others(2): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139615829 | |||||
| chr5:139616037
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304+1071T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616037 | ||||||
| chr5:139616077
|
A | C | 20 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0037others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.304+1111A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616077 | ||||||
| chr5:139616197
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304+1231C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616197 | ||||||
| chr5:139616204
|
A | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.304+1238A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616204 | ||||||
| chr5:139616366
|
G | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.304+1400G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616366 | ||||||
| chr5:139616556
|
A | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304+1590A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616556 | ||||||
| chr5:139616557
|
C | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304+1591C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616557 | ||||||
| chr5:139616558
|
G | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304+1592G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616558 | ||||||
| chr5:139616633
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.304+1667T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139616633 | ||||||
| chr5:139617054
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01167.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.304+2088G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139617054 | ||||||
| chr5:139617326
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.304+2360A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139617326 | ||||||
| chr5:139617370
|
A | AT | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0021others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.304+2427dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139617370 | |||||
| chr5:139617370
|
A | ATT | 6 | a0001c0001t0001g0059a0001c0001t0001g0196a0001c0001t0001g0210others(3): Show | 6 | HG01106.hp1 HG02486.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.304+2426_304+2427d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139617370 | |||||
| chr5:139617370
|
AT | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(8): Show | 11 | HG01099.hp1 HG01167.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+2427delT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139617370 | |||||
| chr5:139617470
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304+2504G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139617470 | ||||||
| chr5:139617485
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.304+2519T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139617485 | ||||||
| chr5:139617842
|
C | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.304+2876C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139617842 | ||||||
| chr5:139617953
|
T | TA | 29 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(26): Show | 29 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.304+2996dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139617953 | |||||
| chr5:139618042
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.304+3076C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618042 | ||||||
| chr5:139618066
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.304+3100C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618066 | ||||||
| chr5:139618118
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.304+3152G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618118 | ||||||
| chr5:139618231
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.304+3265C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618231 | ||||||
| chr5:139618612
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.304+3646G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618612 | ||||||
| chr5:139618654
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.304+3688T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618654 | ||||||
| chr5:139618991
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+4025A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139618991 | ||||||
| chr5:139619395
|
C | CA | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(92): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.305-3958dupA | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139619395 | |||||
| chr5:139619478
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.305-3890G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139619478 | ||||||
| chr5:139619592
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305-3776G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139619592 | ||||||
| chr5:139619788
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-3580G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139619788 | ||||||
| chr5:139619817
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0224 | 2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.305-3551C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139619817 | ||||||
| chr5:139619856
|
T | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.305-3512T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139619856 | ||||||
| chr5:139619863
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00741.hp1 HG01167.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-3496_305-3495i others(16): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 139619863 | |||||
| chr5:139620022
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.305-3346G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139620022 | ||||||
| chr5:139620041
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.305-3327G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139620041 | ||||||
| chr5:139620144
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0078 | 2 | NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.305-3224C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139620144 | ||||||
| chr5:139620847
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.305-2521G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139620847 | ||||||
| chr5:139621002
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.305-2366C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139621002 | ||||||
| chr5:139621010
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.305-2358C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139621010 | ||||||
| chr5:139621169
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0183 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.305-2199G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139621169 | ||||||
| chr5:139621355
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.305-2013G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139621355 | ||||||
| chr5:139621734
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(25): Show | 28 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.305-1634C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139621734 | ||||||
| chr5:139621862
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(22): Show | 25 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.305-1506A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139621862 | ||||||
| chr5:139622200
|
A | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0001g0167others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-1168A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622200 | ||||||
| chr5:139622245
|
A | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(25): Show | 28 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.305-1123A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622245 | ||||||
| chr5:139622290
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.305-1078G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622290 | ||||||
| chr5:139622313
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.305-1055C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622313 | ||||||
| chr5:139622495
|
C | T | 1 | a0001c0001t0003g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.305-873C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622495 | ||||||
| chr5:139622523
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.305-845A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622523 | ||||||
| chr5:139622672
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.305-696G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622672 | ||||||
| chr5:139622704
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.305-664A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622704 | ||||||
| chr5:139622751
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.305-617G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622751 | ||||||
| chr5:139622941
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.305-427C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139622941 | ||||||
| chr5:139623029
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.305-339C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 5/6 | chr5 | 139623029 | ||||||
| chr5:139623631
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(4): Show | 7 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.398+170A>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623631 | ||||||
| chr5:139623688
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0004g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.398+235_398+246dup others(12): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139623688 | |||||
| chr5:139623692
|
T | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+231T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623692 | ||||||
| chr5:139623700
|
G | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0061 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.398+239G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623700 | ||||||
| chr5:139623704
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.398+243T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623704 | ||||||
| chr5:139623778
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0092 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.398+317G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623778 | ||||||
| chr5:139623887
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.398+426T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623887 | ||||||
| chr5:139623910
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.398+449C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139623910 | ||||||
| chr5:139624011
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.398+550T>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139624011 | ||||||
| chr5:139624125
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.398+664T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139624125 | ||||||
| chr5:139624478
|
G | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0078 | 2 | NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.398+1017G>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139624478 | ||||||
| chr5:139624904
|
G | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0194others(31): Show | 34 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.398+1443G>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139624904 | ||||||
| chr5:139624984
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+1523A>G | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139624984 | ||||||
| chr5:139625042
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.398+1581C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625042 | ||||||
| chr5:139625051
|
C | CT | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.398+1591dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625051 | |||||
| chr5:139625137
|
A | C | 1 | a0001c0001t0002g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.399-1619A>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625137 | ||||||
| chr5:139625172
|
C | CCCAGCCT others(41): Show |
30 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0056others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.399-1537_399-1490d others(50): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625172 | |||||
| chr5:139625172
|
C | CCCAGCCT others(89): Show |
1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.399-1490_399-1489i others(98): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625172 | |||||
| chr5:139625172
|
CCCAGCCT others(41): Show |
C | 3 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0078 | 3 | NA18973.hp1 NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.399-1537_399-1490d others(50): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625172 | |||||
| chr5:139625276
|
G | GT | 30 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 30 | HG00597.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.399-1461dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625276 | |||||
| chr5:139625309
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.399-1447C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625309 | ||||||
| chr5:139625390
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(34): Show | 38 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.399-1366C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625390 | ||||||
| chr5:139625404
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.399-1352C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625404 | ||||||
| chr5:139625430
|
AC | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0194a0001c0001t0001g0195others(19): Show | 22 | HG00280.hp1 HG00597.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.399-1316delC | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625430 | |||||
| chr5:139625439
|
C | CTTT | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.399-1317_399-1316i others(5): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625439 | ||||||
| chr5:139625440
|
C | CCT | 72 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(69): Show | 72 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.399-1316_399-1315i others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625440 | ||||||
| chr5:139625440
|
C | CCTT | 16 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0048others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.399-1316_399-1315i others(5): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625440 | ||||||
| chr5:139625440
|
C | CT | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(54): Show | 57 | HG00280.hp2 HG00733.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.399-1295dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625440 | |||||
| chr5:139625440
|
C | CTT | 21 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0039others(18): Show | 22 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.399-1296_399-1295d others(4): Show |
UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625440 | |||||
| chr5:139625440
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0088others(4): Show | 7 | HG02622.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.399-1316C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625440 | ||||||
| chr5:139625441
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.399-1315T>C | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625441 | ||||||
| chr5:139625610
|
A | AT | 30 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0194others(27): Show | 30 | HG00280.hp1 HG00597.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.399-1133dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139625610 | |||||
| chr5:139625713
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00741.hp1 HG01167.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.399-1043C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625713 | ||||||
| chr5:139625811
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | HG03669.hp2 HG03688.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.399-945G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625811 | ||||||
| chr5:139625972
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01099.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.399-784C>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139625972 | ||||||
| chr5:139626125
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.399-631G>A | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139626125 | ||||||
| chr5:139626131
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.399-625C>T | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | chr5 | 139626131 | ||||||
| chr5:139626667
|
C | CT | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01167.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.399-87dupT | UBE2D2 | ENSG00000131508.17 | transcript | ENST00000398733.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 139626667 |