Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 140739 |
| ensemblid | ENSG00000184182.19 |
| hgncid | 12480 |
| symbol | UBE2F |
| name | ubiquitin conjugating enzyme E2 F (putative) |
| refseq_nuc | NM_080678.3 |
| refseq_prot | NP_542409.1 |
| ensembl_nuc | ENST00000272930.9 |
| ensembl_prot | ENSP00000272930.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 237967014 |
| end | 238042782 |
| strand | + |
| ver | v1.2 |
| region | chr2:237967014-238042782 |
| region5000 | chr2:237962014-238047782 |
| regionname0 | UBE2F_chr2_237967014_238042782 |
| regionname5000 | UBE2F_chr2_237962014_238047782 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 555 | 324 | 83 | 58 | 140 | 10 | 32 | UBE2F_chr2_237962014_238047782 | UBE2F | ATGCT others(550): Show |
chr2 | 237962014 | 238047782 | ||
| a0001c0002 | 0/1 | 555 | 39 | 0 | 4 | 26 | 2 | 6 | UBE2F_chr2_237962014_238047782 | UBE2F | ATGCT others(550): Show |
chr2 | 237962014 | 238047782 | ||
| a0001c0003 | 0/0 | 555 | 5 | 5 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ATGCT others(550): Show |
chr2 | 237962014 | 238047782 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2137 | 252 | 50 | 43 | 133 | 7 | 19 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0002 | 1/0 | 2137 | 53 | 22 | 11 | 4 | 3 | 12 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0003 | 0/0 | 2137 | 6 | 6 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0004 | 0/0 | 2137 | 3 | 0 | 2 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0005 | 0/0 | 2137 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0006 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0007 | 0/0 | 2137 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0008 | 0/0 | 2137 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0009 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0010 | 0/0 | 2137 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0011 | 0/0 | 2137 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0012 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0001t0013 | 0/0 | 2137 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0002t0001 | 0/1 | 2137 | 39 | 0 | 4 | 26 | 2 | 6 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| a0001c0003t0001 | 0/0 | 2137 | 5 | 5 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | ACTTC others(2132): Show |
chr2 | 237962014 | 238047782 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0011g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0001t0013g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0141 | EUR | GBR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0333 | EUR | GBR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0095 | EUR | FIN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01071 | hp1 | a0001 | c0001 | t0011 | g0280 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0290 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | IBS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0334 | EUR | IBS | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0170 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0291 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0246 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CDX | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0169 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0344 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0310 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0346 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0339 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0340 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0331 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0330 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0343 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0326 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0345 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | YRI | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | CHB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18973 | hp2 | a0001 | c0001 | t0008 | g0009 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0167 | AFR | LWK | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19056 | hp2 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | YRI | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | TSI | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0114 | SAS | GIH | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | USA | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0208 | REF | REF | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0015 | REF | REF | UBE2F_chr2_237962014_238047782 | UBE2F | chr2 | 237962014 | 238047782 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237987985 | T | C | 1 | a0001c0003 | 5 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.141T>C | p.Asn47Asn | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/10 | 276/2137 | 141/558 | 47/185 | chr2 | 237987985 | |||
| chr2:237994757 | G | A | 1 | a0001c0002 | 38 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(35): Show |
synonymous_variant | LOW | c.162G>A | p.Val54Val | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/10 | 297/2137 | 162/558 | 54/185 | chr2 | 237994757 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237967057 | C | A | 1 | a0001c0001t0006 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/10 | 6051 | chr2 | 237967057 | ||||||
| chr2:237967074 | G | A | 1 | a0001c0001t0007 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/10 | 6034 | chr2 | 237967074 | ||||||
| chr2:237967094 | T | C | 1 | a0001c0001t0008 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/10 | 6014 | chr2 | 237967094 | ||||||
| chr2:238041375 | C | A | 1 | a0001c0001t0009 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 37 | chr2 | 238041375 | ||||||
| chr2:238041660 | C | T | 1 | a0001c0001t0013 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 322 | chr2 | 238041660 | ||||||
| chr2:238041707 | A | G | 1 | a0001c0001t0004 | 3 | HG01167.hp1 HG01952.hp2 NA18997.hp1 |
3_prime_UTR_variant | MODIFIER | c.*369A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 369 | chr2 | 238041707 | ||||||
| chr2:238042123 | G | T | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 785 | chr2 | 238042123 | ||||||
| chr2:238042245 | T | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*907T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 907 | chr2 | 238042245 | ||||||
| chr2:238042409 | G | C | 1 | a0001c0001t0010 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 1071 | chr2 | 238042409 | ||||||
| chr2:238042417 | C | T | 1 | a0001c0001t0005 | 2 | HG02559.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1079C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 1079 | chr2 | 238042417 | ||||||
| chr2:238042454 | G | C | 1 | a0001c0001t0011 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1116G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 1116 | chr2 | 238042454 | ||||||
| chr2:238042523 | A | C | 1 | a0001c0001t0003 | 6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1185A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 1185 | chr2 | 238042523 | ||||||
| chr2:238042642 | G | A | 1 | a0001c0001t0003 | 6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1304G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 10/10 | 1304 | chr2 | 238042642 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237967268 | T | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.-17+136T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967268 | |||||||
| chr2:237967316 | G | GGGGCCGC | 5 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0315 others(2): Show |
5 | HG02004.hp2 NA18973.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+200_-17+206dup others(7): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237967316 | ||||||
| chr2:237967384 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+252C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967384 | |||||||
| chr2:237967557 | G | T | 1 | a0001c0001t0001g0306 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-17+425G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967557 | |||||||
| chr2:237967584 | C | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+452C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967584 | |||||||
| chr2:237967788 | A | C | 1 | a0001c0001t0001g0305 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-17+656A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967788 | |||||||
| chr2:237967832 | G | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-17+700G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967832 | |||||||
| chr2:237967903 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-17+771T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237967903 | |||||||
| chr2:237968265 | C | G | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17+1133C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968265 | |||||||
| chr2:237968338 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
11 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17+1206G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968338 | |||||||
| chr2:237968381 | C | T | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+1249C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968381 | |||||||
| chr2:237968386 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.-17+1254A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968386 | |||||||
| chr2:237968499 | C | T | 1 | a0001c0002t0001g0292 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17+1367C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968499 | |||||||
| chr2:237968528 | C | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17+1396C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968528 | |||||||
| chr2:237968767 | A | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-17+1635A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968767 | |||||||
| chr2:237968772 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17+1640G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968772 | |||||||
| chr2:237968820 | A | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17+1688A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237968820 | |||||||
| chr2:237969098 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-17+1966A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237969098 | |||||||
| chr2:237969261 | C | T | 2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-17+2129C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237969261 | |||||||
| chr2:237969272 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(24): Show |
30 | HG00423.hp1 HG00621.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.-17+2140G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237969272 | |||||||
| chr2:237969542 | A | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(62): Show |
68 | HG00423.hp1 HG00621.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17+2410A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237969542 | |||||||
| chr2:237969601 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17+2469G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237969601 | |||||||
| chr2:237970016 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
64 | HG00423.hp1 HG00621.hp1 HG01358.hp1 others(61): Show |
intron_variant | MODIFIER | c.-17+2884G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970016 | |||||||
| chr2:237970062 | A | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01255.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-17+2930A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970062 | |||||||
| chr2:237970076 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+2944C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970076 | |||||||
| chr2:237970150 | C | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-16-2942C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970150 | |||||||
| chr2:237970173 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16-2919C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970173 | |||||||
| chr2:237970362 | A | C | 3 | a0001c0001t0004g0289 a0001c0001t0004g0290 a0001c0001t0004g0291 |
3 | HG01167.hp1 HG01952.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.-16-2730A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970362 | |||||||
| chr2:237970523 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-16-2569A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970523 | |||||||
| chr2:237970660 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-16-2432G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970660 | |||||||
| chr2:237970799 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0006g0056 |
3 | HG01358.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-16-2293C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970799 | |||||||
| chr2:237970812 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02165.hp1 NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-16-2280A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970812 | |||||||
| chr2:237970849 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-2243C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970849 | |||||||
| chr2:237970895 | T | G | 2 | a0001c0001t0001g0009 a0001c0001t0008g0009 |
2 | NA18973.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-16-2197T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970895 | |||||||
| chr2:237970998 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-2094C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237970998 | |||||||
| chr2:237971005 | G | T | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-16-2087G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971005 | |||||||
| chr2:237971274 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-16-1818G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971274 | |||||||
| chr2:237971387 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-16-1705A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971387 | |||||||
| chr2:237971389 | C | G | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16-1703C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971389 | |||||||
| chr2:237971418 | C | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-16-1674C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971418 | |||||||
| chr2:237971503 | TAGTAGAG others(4): Show |
T | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16-1588_-16-1578d others(13): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971503 | |||||||
| chr2:237971504 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.-16-1588A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971504 | |||||||
| chr2:237971517 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16-1575T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971517 | |||||||
| chr2:237971636 | T | C | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-1456T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971636 | |||||||
| chr2:237971673 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-16-1419G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971673 | |||||||
| chr2:237971733 | C | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-16-1359C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971733 | |||||||
| chr2:237971739 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-16-1353G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971739 | |||||||
| chr2:237971745 | T | TTGTTACA others(1): Show |
305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-16-1345_-16-1338d others(10): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237971745 | ||||||
| chr2:237971799 | T | TTAA | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-16-1291_-16-1289d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237971799 | ||||||
| chr2:237971888 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-16-1204G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237971888 | |||||||
| chr2:237972078 | G | A | 1 | a0001c0001t0002g0318 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-16-1014G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972078 | |||||||
| chr2:237972099 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-16-993T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972099 | |||||||
| chr2:237972106 | C | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-986C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972106 | |||||||
| chr2:237972165 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-16-927A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972165 | |||||||
| chr2:237972167 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-925C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972167 | |||||||
| chr2:237972466 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-16-626G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972466 | |||||||
| chr2:237972513 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-16-579T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972513 | |||||||
| chr2:237972541 | AT | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(30): Show |
36 | HG00423.hp2 HG01081.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.-16-524delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237972541 | ||||||
| chr2:237972541 | ATT | A | 84 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0051 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-16-525_-16-524del others(2): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237972541 | ||||||
| chr2:237972541 | ATTT | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
199 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-16-526_-16-524del others(3): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237972541 | ||||||
| chr2:237972541 | ATTTT | A | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0068 others(8): Show |
11 | HG01168.hp1 HG01515.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-527_-16-524del others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 237972541 | ||||||
| chr2:237972544 | T | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0303 others(1): Show |
4 | HG00642.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-548T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972544 | |||||||
| chr2:237972545 | T | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(23): Show |
28 | HG00423.hp2 HG01081.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.-16-547T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972545 | |||||||
| chr2:237972545 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-16-547T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972545 | |||||||
| chr2:237972546 | T | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0051 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-16-546T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972546 | |||||||
| chr2:237972547 | T | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
189 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.-16-545T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972547 | |||||||
| chr2:237972548 | T | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0068 others(9): Show |
12 | HG01168.hp1 HG01515.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.-16-544T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972548 | |||||||
| chr2:237972549 | T | A | 2 | a0001c0001t0001g0051 a0001c0002t0001g0206 |
2 | HG03831.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-16-543T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972549 | |||||||
| chr2:237972550 | T | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(76): Show |
82 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-16-542T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972550 | |||||||
| chr2:237972551 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0068 others(3): Show |
6 | NA18946.hp1 NA18948.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-541T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972551 | |||||||
| chr2:237972553 | T | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
32 | HG00140.hp2 HG00621.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-539T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972553 | |||||||
| chr2:237972584 | C | T | 30 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(27): Show |
33 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.-16-508C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972584 | |||||||
| chr2:237972615 | A | G | 1 | a0001c0003t0001g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-16-477A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972615 | |||||||
| chr2:237972626 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0029 others(78): Show |
83 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-16-466C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972626 | |||||||
| chr2:237972676 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.-16-416G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972676 | |||||||
| chr2:237972827 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-16-265A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972827 | |||||||
| chr2:237972892 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-16-200A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972892 | |||||||
| chr2:237972916 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-16-176A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 1/9 | chr2 | 237972916 | |||||||
| chr2:237973297 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+72A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237973297 | |||||||
| chr2:237973448 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+223T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237973448 | |||||||
| chr2:237973455 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+230G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237973455 | |||||||
| chr2:237973559 | T | A | 1 | a0001c0002t0001g0105 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.118+334T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237973559 | |||||||
| chr2:237973911 | A | G | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+686A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237973911 | |||||||
| chr2:237974022 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.118+797G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974022 | |||||||
| chr2:237974033 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.118+808A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974033 | |||||||
| chr2:237974093 | C | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.118+868C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974093 | |||||||
| chr2:237974111 | A | T | 1 | a0001c0001t0011g0280 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.118+886A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974111 | |||||||
| chr2:237974160 | A | AT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
89 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.118+949dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237974160 | ||||||
| chr2:237974160 | AT | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(25): Show |
31 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.118+949delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237974160 | ||||||
| chr2:237974411 | A | C | 1 | a0001c0002t0001g0156 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.118+1186A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974411 | |||||||
| chr2:237974474 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.118+1249G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974474 | |||||||
| chr2:237974501 | GT | G | 12 | a0001c0001t0001g0279 a0001c0001t0002g0293 a0001c0001t0002g0294 others(9): Show |
12 | HG01261.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.118+1289delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237974501 | ||||||
| chr2:237974501 | GTT | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
119 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.118+1288_118+1289d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237974501 | ||||||
| chr2:237974513 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.118+1288T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974513 | |||||||
| chr2:237974514 | T | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0202 a0001c0001t0001g0226 |
3 | HG03139.hp1 NA18956.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.118+1289T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974514 | |||||||
| chr2:237974514 | TG | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.118+1290delG | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974514 | |||||||
| chr2:237974515 | G | T | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0106 others(11): Show |
14 | HG01081.hp2 HG01261.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+1290G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974515 | |||||||
| chr2:237974519 | T | G | 1 | a0001c0002t0001g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.118+1294T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974519 | |||||||
| chr2:237974521 | T | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02027.hp2 HG02056.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+1296T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974521 | |||||||
| chr2:237974550 | G | A | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+1325G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974550 | |||||||
| chr2:237974605 | C | G | 1 | a0001c0002t0001g0163 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.118+1380C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974605 | |||||||
| chr2:237974658 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118+1433C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974658 | |||||||
| chr2:237974659 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG00597.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.118+1434G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974659 | |||||||
| chr2:237974667 | C | T | 2 | a0001c0002t0001g0316 a0001c0002t0001g0317 |
2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.118+1442C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974667 | |||||||
| chr2:237974761 | C | A | 1 | a0001c0003t0001g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.118+1536C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974761 | |||||||
| chr2:237974901 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0084 others(24): Show |
28 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.118+1676G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237974901 | |||||||
| chr2:237974901 | G | GGCCTCCC others(116): Show |
1 | a0001c0001t0001g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+1692_118+1814d others(125): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237974901 | ||||||
| chr2:237975033 | A | AAGTGCTA others(116): Show |
2 | a0001c0001t0001g0009 a0001c0001t0008g0009 |
2 | NA18973.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.118+1814_118+1815i others(125): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237975033 | ||||||
| chr2:237975105 | A | AT | 10 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0003g0307 others(7): Show |
10 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+1895dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237975105 | ||||||
| chr2:237975105 | AT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0020 others(42): Show |
48 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.118+1895delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237975105 | ||||||
| chr2:237975106 | T | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(55): Show |
61 | HG00423.hp1 HG00621.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.118+1881T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975106 | |||||||
| chr2:237975107 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+1882T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975107 | |||||||
| chr2:237975107 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(55): Show |
61 | HG00423.hp1 HG00621.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.118+1882T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975107 | |||||||
| chr2:237975108 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+1883T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975108 | |||||||
| chr2:237975116 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+1891T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975116 | |||||||
| chr2:237975138 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+1913T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975138 | |||||||
| chr2:237975139 | A | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+1914A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975139 | |||||||
| chr2:237975195 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+1970G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975195 | |||||||
| chr2:237975312 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.118+2087G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975312 | |||||||
| chr2:237975324 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.118+2099G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975324 | |||||||
| chr2:237975410 | A | C | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+2185A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975410 | |||||||
| chr2:237975620 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+2395G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975620 | |||||||
| chr2:237975642 | G | A | 1 | a0001c0002t0001g0124 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.118+2417G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975642 | |||||||
| chr2:237975653 | G | A | 3 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 |
3 | HG01081.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.118+2428G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975653 | |||||||
| chr2:237975658 | A | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
59 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(56): Show |
intron_variant | MODIFIER | c.118+2433A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237975658 | |||||||
| chr2:237975941 | A | ACTCTTTT others(262): Show |
2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG01081.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.118+2727_118+2728i others(271): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237975941 | ||||||
| chr2:237975941 | A | ACTCTTTT others(289): Show |
1 | a0001c0001t0002g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+2727_118+2728i others(298): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237975941 | ||||||
| chr2:237976008 | T | C | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+2783T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976008 | |||||||
| chr2:237976073 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02647.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.118+2848G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976073 | |||||||
| chr2:237976195 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.118+2970C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976195 | |||||||
| chr2:237976301 | A | G | 1 | a0001c0001t0011g0280 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.118+3076A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976301 | |||||||
| chr2:237976590 | G | GT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(6): Show |
11 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.118+3366dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237976590 | ||||||
| chr2:237976667 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+3442G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976667 | |||||||
| chr2:237976851 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.118+3626C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976851 | |||||||
| chr2:237976873 | T | G | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.118+3648T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976873 | |||||||
| chr2:237976895 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+3670G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976895 | |||||||
| chr2:237976950 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.118+3725G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976950 | |||||||
| chr2:237976987 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.118+3762A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237976987 | |||||||
| chr2:237977030 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.118+3805G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977030 | |||||||
| chr2:237977032 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.118+3807G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977032 | |||||||
| chr2:237977086 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.118+3861C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977086 | |||||||
| chr2:237977109 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118+3884G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977109 | |||||||
| chr2:237977150 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(28): Show |
34 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.118+3925A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977150 | |||||||
| chr2:237977215 | AAGAAGGT others(9): Show |
A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3997_118+4012d others(18): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237977215 | ||||||
| chr2:237977219 | A | AG | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+3996dupG | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237977219 | ||||||
| chr2:237977219 | AGGTCTCA others(10): Show |
A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
306 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.118+4010_118+4026d others(19): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237977219 | ||||||
| chr2:237977248 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
59 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(56): Show |
intron_variant | MODIFIER | c.118+4023G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977248 | |||||||
| chr2:237977293 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.118+4068C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977293 | |||||||
| chr2:237977335 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+4110C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977335 | |||||||
| chr2:237977550 | C | T | 5 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0315 others(2): Show |
5 | HG02004.hp2 NA18973.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+4325C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977550 | |||||||
| chr2:237977650 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0281 |
2 | HG01516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.118+4425G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977650 | |||||||
| chr2:237977769 | G | A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+4544G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977769 | |||||||
| chr2:237977839 | T | C | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+4614T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977839 | |||||||
| chr2:237977866 | T | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.118+4641T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977866 | |||||||
| chr2:237977890 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.118+4665C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977890 | |||||||
| chr2:237977987 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.118+4762G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237977987 | |||||||
| chr2:237978021 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.118+4796C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978021 | |||||||
| chr2:237978038 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.118+4813C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978038 | |||||||
| chr2:237978386 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(24): Show |
30 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.118+5161G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978386 | |||||||
| chr2:237978692 | T | A | 1 | a0001c0001t0002g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118+5467T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978692 | |||||||
| chr2:237978726 | G | A | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+5501G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978726 | |||||||
| chr2:237978761 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+5536G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978761 | |||||||
| chr2:237978773 | G | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
22 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+5548G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978773 | |||||||
| chr2:237978895 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118+5670C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978895 | |||||||
| chr2:237978909 | AGGGCAGA others(10): Show |
A | 1 | a0001c0001t0001g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.118+5685_118+5701d others(19): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978909 | |||||||
| chr2:237978933 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.118+5708C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978933 | |||||||
| chr2:237978957 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118+5732C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237978957 | |||||||
| chr2:237979017 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.118+5792A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237979017 | |||||||
| chr2:237979102 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118+5877C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237979102 | |||||||
| chr2:237979283 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.118+6058C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237979283 | |||||||
| chr2:237979472 | C | T | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+6247C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237979472 | |||||||
| chr2:237979560 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+6335C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237979560 | |||||||
| chr2:237980048 | G | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG02145.hp2 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+6823G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980048 | |||||||
| chr2:237980061 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.118+6836G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980061 | |||||||
| chr2:237980084 | T | TA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0226 a0001c0001t0001g0231 others(3): Show |
7 | NA18953.hp2 NA18956.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6862dupA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237980084 | ||||||
| chr2:237980183 | G | A | 1 | a0001c0003t0001g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118+6958G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980183 | |||||||
| chr2:237980187 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.118+6962A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980187 | |||||||
| chr2:237980330 | T | C | 2 | a0001c0002t0001g0027 a0001c0002t0001g0163 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.118+7105T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980330 | |||||||
| chr2:237980332 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(124): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.118+7107T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980332 | |||||||
| chr2:237980407 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.118+7182C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980407 | |||||||
| chr2:237980614 | A | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-7349A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980614 | |||||||
| chr2:237980624 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.119-7339G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980624 | |||||||
| chr2:237980625 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-7338C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980625 | |||||||
| chr2:237980670 | T | A | 1 | a0001c0001t0002g0332 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.119-7293T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980670 | |||||||
| chr2:237980711 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.119-7252C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980711 | |||||||
| chr2:237980758 | T | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-7205T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980758 | |||||||
| chr2:237980854 | G | A | 6 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(3): Show |
7 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-7109G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237980854 | |||||||
| chr2:237981047 | G | A | 6 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(3): Show |
7 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-6916G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981047 | |||||||
| chr2:237981165 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.119-6798T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981165 | |||||||
| chr2:237981183 | T | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-6780T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981183 | |||||||
| chr2:237981367 | GA | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-6595delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981367 | |||||||
| chr2:237981394 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(34): Show |
40 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.119-6569G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981394 | |||||||
| chr2:237981413 | G | A | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-6550G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981413 | |||||||
| chr2:237981614 | CT | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0002g0013 others(15): Show |
21 | HG00099.hp2 HG01169.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.119-6319delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981614 | CTT | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(35): Show |
40 | HG00323.hp2 HG00738.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.119-6320_119-6319d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981614 | CTTT | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
85 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.119-6321_119-6319d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981614 | CTTTT | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
64 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-6322_119-6319d others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981614 | CTTTTT | C | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(108): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.119-6323_119-6319d others(7): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981614 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 |
3 | HG01081.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.119-6329_119-6319d others(13): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981614 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-6333_119-6319d others(17): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237981614 | ||||||
| chr2:237981674 | T | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.119-6289T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981674 | |||||||
| chr2:237981749 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.119-6214C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981749 | |||||||
| chr2:237981864 | C | T | 3 | a0001c0003t0001g0168 a0001c0003t0001g0169 a0001c0003t0001g0170 |
3 | HG01891.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.119-6099C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981864 | |||||||
| chr2:237981966 | A | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-5997A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237981966 | |||||||
| chr2:237982036 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-5927A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982036 | |||||||
| chr2:237982100 | G | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-5863G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982100 | |||||||
| chr2:237982168 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
22 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-5795G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982168 | |||||||
| chr2:237982204 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.119-5759A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982204 | |||||||
| chr2:237982264 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.119-5699C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982264 | |||||||
| chr2:237982289 | G | C | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.119-5674G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982289 | |||||||
| chr2:237982317 | C | G | 2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.119-5646C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982317 | |||||||
| chr2:237982338 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0010g0186 |
3 | NA18952.hp2 NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.119-5625C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982338 | |||||||
| chr2:237982489 | G | A | 22 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(19): Show |
22 | HG00140.hp2 HG00558.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.119-5474G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982489 | |||||||
| chr2:237982949 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.119-5014A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237982949 | |||||||
| chr2:237983004 | T | G | 1 | a0001c0002t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.119-4959T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237983004 | |||||||
| chr2:237983266 | C | T | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-4697C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237983266 | |||||||
| chr2:237983630 | G | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.119-4333G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237983630 | |||||||
| chr2:237983708 | G | A | 7 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-4255G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237983708 | |||||||
| chr2:237983802 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.119-4161C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237983802 | |||||||
| chr2:237984050 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.119-3913T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984050 | |||||||
| chr2:237984128 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.119-3835G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984128 | |||||||
| chr2:237984337 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.119-3626A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984337 | |||||||
| chr2:237984344 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.119-3619A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984344 | |||||||
| chr2:237984541 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.119-3422C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984541 | |||||||
| chr2:237984658 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.119-3305C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984658 | |||||||
| chr2:237984720 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.119-3243T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984720 | |||||||
| chr2:237984760 | T | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0086 others(30): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.119-3203T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984760 | |||||||
| chr2:237984925 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.119-3038A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237984925 | |||||||
| chr2:237984996 | CA | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.119-2949delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237984996 | ||||||
| chr2:237984996 | CAA | C | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00642.hp1 HG01358.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.119-2950_119-2949d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237984996 | ||||||
| chr2:237984996 | CAAA | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0171 a0001c0001t0001g0184 others(5): Show |
8 | HG00621.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-2951_119-2949d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237984996 | ||||||
| chr2:237984996 | CAAAA | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
97 | HG00423.hp1 HG01255.hp1 HG01257.hp2 others(94): Show |
intron_variant | MODIFIER | c.119-2952_119-2949d others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237984996 | ||||||
| chr2:237985089 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.119-2874C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985089 | |||||||
| chr2:237985097 | G | T | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.119-2866G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985097 | |||||||
| chr2:237985175 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.119-2788A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985175 | |||||||
| chr2:237985178 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-2785G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985178 | |||||||
| chr2:237985206 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.119-2757T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985206 | |||||||
| chr2:237985210 | T | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.119-2753T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985210 | |||||||
| chr2:237985410 | C | T | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-2553C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985410 | |||||||
| chr2:237985507 | C | G | 1 | a0001c0001t0002g0346 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.119-2456C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985507 | |||||||
| chr2:237985814 | T | C | 1 | a0001c0002t0001g0207 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.119-2149T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985814 | |||||||
| chr2:237985892 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-2071T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237985892 | |||||||
| chr2:237986027 | A | AT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(8): Show |
13 | HG01346.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.119-1927dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237986027 | ||||||
| chr2:237986129 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-1834T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986129 | |||||||
| chr2:237986142 | C | CT | 9 | a0001c0001t0001g0008 a0001c0001t0003g0310 a0001c0001t0003g0311 others(6): Show |
10 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-1805dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237986142 | ||||||
| chr2:237986142 | CT | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.119-1805delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 237986142 | ||||||
| chr2:237986143 | T | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02155.hp2 NA18990.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.119-1820T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986143 | |||||||
| chr2:237986144 | T | C | 6 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-1819T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986144 | |||||||
| chr2:237986228 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.119-1735C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986228 | |||||||
| chr2:237986311 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.119-1652C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986311 | |||||||
| chr2:237986394 | A | G | 1 | a0001c0001t0002g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-1569A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986394 | |||||||
| chr2:237986429 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
11 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-1534C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986429 | |||||||
| chr2:237986442 | C | T | 1 | a0001c0001t0002g0345 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.119-1521C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986442 | |||||||
| chr2:237986583 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-1380G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986583 | |||||||
| chr2:237986736 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.119-1227T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986736 | |||||||
| chr2:237986773 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.119-1190C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986773 | |||||||
| chr2:237986851 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.119-1112A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986851 | |||||||
| chr2:237986863 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.119-1100G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986863 | |||||||
| chr2:237986865 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.119-1098G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986865 | |||||||
| chr2:237986970 | G | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.119-993G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237986970 | |||||||
| chr2:237987256 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.119-707G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987256 | |||||||
| chr2:237987371 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.119-592G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987371 | |||||||
| chr2:237987496 | C | T | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.119-467C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987496 | |||||||
| chr2:237987512 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.119-451C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987512 | |||||||
| chr2:237987766 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.119-197T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987766 | |||||||
| chr2:237987852 | C | CA | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(84): Show |
94 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.119-111_119-110ins others(1): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987852 | |||||||
| chr2:237987852 | C | CAT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
87 | HG00423.hp1 HG00621.hp1 HG01346.hp2 others(84): Show |
intron_variant | MODIFIER | c.119-111_119-110ins others(2): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987852 | |||||||
| chr2:237987852 | C | CATT | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.119-111_119-110ins others(3): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987852 | |||||||
| chr2:237987852 | C | CATTT | 5 | a0001c0001t0001g0080 a0001c0001t0001g0109 a0001c0001t0001g0119 others(2): Show |
5 | HG01109.hp2 HG03490.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-111_119-110ins others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987852 | |||||||
| chr2:237987852 | C | CATTTTTT | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-111_119-110ins others(7): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987852 | |||||||
| chr2:237987853 | T | A | 1 | a0001c0001t0001g0274 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.119-110T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987853 | |||||||
| chr2:237987932 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.119-31A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987932 | |||||||
| chr2:237987949 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.119-14C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 2/9 | chr2 | 237987949 | |||||||
| chr2:237988012 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.148+20A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988012 | |||||||
| chr2:237988069 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.148+77G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988069 | |||||||
| chr2:237988279 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.148+287C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988279 | |||||||
| chr2:237988282 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0006g0056 |
3 | HG01358.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.148+290T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988282 | |||||||
| chr2:237988316 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.148+324C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988316 | |||||||
| chr2:237988335 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.148+343C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988335 | |||||||
| chr2:237988360 | A | G | 2 | a0001c0001t0002g0343 a0001c0001t0002g0344 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.148+368A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988360 | |||||||
| chr2:237988409 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+417C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988409 | |||||||
| chr2:237988447 | CA | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.148+469delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237988447 | ||||||
| chr2:237988462 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.148+470T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988462 | |||||||
| chr2:237988592 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.148+600G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988592 | |||||||
| chr2:237988615 | T | TA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0020 others(41): Show |
47 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(44): Show |
intron_variant | MODIFIER | c.148+642dupA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237988615 | ||||||
| chr2:237988615 | TA | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(9): Show |
13 | HG01168.hp2 HG02080.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.148+642delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237988615 | ||||||
| chr2:237988732 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.148+740G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988732 | |||||||
| chr2:237988790 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.148+798T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988790 | |||||||
| chr2:237988822 | T | C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0071 |
3 | NA18939.hp1 NA18988.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.148+830T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988822 | |||||||
| chr2:237988945 | C | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.148+953C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988945 | |||||||
| chr2:237988964 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.148+972C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237988964 | |||||||
| chr2:237989077 | A | AT | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
63 | HG00423.hp1 HG00621.hp1 HG01358.hp1 others(60): Show |
intron_variant | MODIFIER | c.148+1091dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237989077 | ||||||
| chr2:237989077 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.148+1085A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989077 | |||||||
| chr2:237989113 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.148+1121C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989113 | |||||||
| chr2:237989197 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0261 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.148+1205A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989197 | |||||||
| chr2:237989292 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.148+1300A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989292 | |||||||
| chr2:237989464 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+1472C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989464 | |||||||
| chr2:237989465 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.148+1473G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989465 | |||||||
| chr2:237989631 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.148+1639G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989631 | |||||||
| chr2:237989735 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.148+1743G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237989735 | |||||||
| chr2:237990111 | CA | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0106 others(12): Show |
16 | HG00735.hp1 HG01081.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.148+2141delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237990111 | ||||||
| chr2:237990111 | CAA | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.148+2140_148+2141d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237990111 | ||||||
| chr2:237990111 | CAAA | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(34): Show |
39 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(36): Show |
intron_variant | MODIFIER | c.148+2139_148+2141d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237990111 | ||||||
| chr2:237990133 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.148+2141A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990133 | |||||||
| chr2:237990167 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.148+2175G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990167 | |||||||
| chr2:237990221 | G | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0237 a0001c0001t0001g0281 |
3 | HG01358.hp2 HG01516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.148+2229G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990221 | |||||||
| chr2:237990403 | CT | C | 15 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0229 others(12): Show |
16 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.148+2426delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237990403 | ||||||
| chr2:237990458 | A | C | 1 | a0001c0001t0001g0259 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.148+2466A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990458 | |||||||
| chr2:237990566 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
15 | HG01346.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.148+2574C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990566 | |||||||
| chr2:237990676 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.148+2684G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990676 | |||||||
| chr2:237990696 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.148+2704G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990696 | |||||||
| chr2:237990738 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.148+2746G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990738 | |||||||
| chr2:237990755 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.148+2763T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990755 | |||||||
| chr2:237990768 | A | T | 2 | a0001c0001t0001g0053 a0001c0001t0002g0331 |
2 | HG01993.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.148+2776A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237990768 | |||||||
| chr2:237991164 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.148+3172C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991164 | |||||||
| chr2:237991191 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0172 |
3 | HG02486.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.148+3199C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991191 | |||||||
| chr2:237991417 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.149-3327G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991417 | |||||||
| chr2:237991561 | A | AT | 6 | a0001c0001t0001g0020 a0001c0002t0001g0147 a0001c0002t0001g0148 others(3): Show |
6 | HG03098.hp1 NA18943.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-3168dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991561 | ||||||
| chr2:237991561 | AT | A | 8 | a0001c0001t0001g0072 a0001c0001t0001g0125 a0001c0001t0001g0174 others(5): Show |
8 | HG01069.hp1 HG01069.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-3168delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991561 | ||||||
| chr2:237991601 | C | CTTTT | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3140_149-3139i others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991601 | ||||||
| chr2:237991609 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0001g0284 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.149-3132_149-3131i others(19): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(12): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0174 |
2 | HG00558.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.149-3132_149-3131i others(21): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(13): Show |
22 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0084 others(19): Show |
23 | HG00140.hp1 HG00423.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-3132_149-3131i others(22): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(14): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0119 |
3 | HG02148.hp2 HG04184.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.149-3132_149-3131i others(23): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(4): Show |
1 | a0001c0001t0001g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-3132_149-3131i others(13): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(9): Show |
14 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0281 others(11): Show |
14 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.149-3132_149-3131i others(18): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(10): Show |
117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.149-3132_149-3131i others(19): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(11): Show |
121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(118): Show |
124 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.149-3132_149-3131i others(20): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(12): Show |
13 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG00621.hp2 HG00735.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.149-3132_149-3131i others(21): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991609 | C | CTTTCTTT others(13): Show |
3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0010g0186 |
3 | HG01257.hp2 HG01258.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.149-3132_149-3131i others(22): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991609 | ||||||
| chr2:237991663 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.149-3081C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991663 | |||||||
| chr2:237991665 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.149-3079C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991665 | |||||||
| chr2:237991671 | C | T | 22 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(19): Show |
22 | HG00140.hp2 HG00558.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.149-3073C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991671 | |||||||
| chr2:237991727 | T | A | 1 | a0001c0001t0002g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.149-3017T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991727 | |||||||
| chr2:237991737 | G | C | 1 | a0001c0001t0002g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.149-3007G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991737 | |||||||
| chr2:237991814 | C | T | 9 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-2930C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991814 | |||||||
| chr2:237991863 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | NA18988.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.149-2881A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991863 | |||||||
| chr2:237991870 | C | CT | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0050 others(120): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.149-2861dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237991870 | ||||||
| chr2:237991957 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0196 a0001c0001t0001g0202 |
3 | NA18944.hp2 NA18961.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.149-2787C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991957 | |||||||
| chr2:237991993 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.149-2751C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237991993 | |||||||
| chr2:237992012 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.149-2732G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992012 | |||||||
| chr2:237992040 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-2704A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992040 | |||||||
| chr2:237992112 | T | TGCC | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | NA18747.hp2 NA19004.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-2631_149-2629d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237992112 | ||||||
| chr2:237992157 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-2587C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992157 | |||||||
| chr2:237992158 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2586G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992158 | |||||||
| chr2:237992187 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.149-2557G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992187 | |||||||
| chr2:237992301 | C | T | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-2443C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992301 | |||||||
| chr2:237992351 | C | T | 9 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0133 others(6): Show |
9 | HG00642.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-2393C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992351 | |||||||
| chr2:237992549 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.149-2195C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992549 | |||||||
| chr2:237992557 | T | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.149-2187T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992557 | |||||||
| chr2:237992575 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.149-2169C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992575 | |||||||
| chr2:237992784 | C | T | 1 | a0001c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.149-1960C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992784 | |||||||
| chr2:237992811 | AT | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0047 |
5 | HG02015.hp1 NA18945.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-1930delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237992811 | ||||||
| chr2:237992830 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.149-1914C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992830 | |||||||
| chr2:237992861 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0125 a0001c0001t0001g0130 |
3 | HG00735.hp2 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.149-1883C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992861 | |||||||
| chr2:237992871 | T | C | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.149-1873T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237992871 | |||||||
| chr2:237992994 | C | CT | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.149-1739dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237992994 | ||||||
| chr2:237993054 | C | G | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.149-1690C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993054 | |||||||
| chr2:237993092 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.149-1652A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993092 | |||||||
| chr2:237993111 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-1633C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993111 | |||||||
| chr2:237993189 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.149-1555C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993189 | |||||||
| chr2:237993241 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-1503C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993241 | |||||||
| chr2:237993256 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.149-1488G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993256 | |||||||
| chr2:237993315 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-1429G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993315 | |||||||
| chr2:237993377 | C | T | 1 | a0001c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.149-1367C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993377 | |||||||
| chr2:237993519 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.149-1225C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993519 | |||||||
| chr2:237993595 | C | T | 1 | a0001c0001t0002g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.149-1149C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993595 | |||||||
| chr2:237993696 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.149-1048G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993696 | |||||||
| chr2:237993808 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.149-936A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237993808 | |||||||
| chr2:237994086 | G | A | 8 | a0001c0001t0001g0239 a0001c0001t0003g0307 a0001c0001t0003g0308 others(5): Show |
8 | HG02004.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-658G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994086 | |||||||
| chr2:237994108 | TC | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-635delC | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994108 | |||||||
| chr2:237994109 | CT | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.149-617delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 237994109 | ||||||
| chr2:237994112 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
25 | HG01346.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-632T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994112 | |||||||
| chr2:237994113 | T | C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0212 a0001c0001t0001g0213 others(12): Show |
16 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-631T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994113 | |||||||
| chr2:237994206 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.149-538G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994206 | |||||||
| chr2:237994213 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.149-531T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994213 | |||||||
| chr2:237994271 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.149-473T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994271 | |||||||
| chr2:237994419 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0226 a0001c0001t0001g0231 others(4): Show |
8 | NA18949.hp1 NA18953.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-325T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994419 | |||||||
| chr2:237994435 | A | G | 3 | a0001c0003t0001g0168 a0001c0003t0001g0169 a0001c0003t0001g0170 |
3 | HG01891.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.149-309A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994435 | |||||||
| chr2:237994668 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.149-76C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 3/9 | chr2 | 237994668 | |||||||
| chr2:237994858 | A | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+49A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237994858 | |||||||
| chr2:237994872 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+63C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237994872 | |||||||
| chr2:237994976 | G | C | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.214+167G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237994976 | |||||||
| chr2:237995289 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.214+480A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995289 | |||||||
| chr2:237995303 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0012g0200 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.214+494T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995303 | |||||||
| chr2:237995315 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.214+506G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995315 | |||||||
| chr2:237995494 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.214+685G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995494 | |||||||
| chr2:237995502 | T | A | 1 | a0001c0001t0002g0326 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.214+693T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995502 | |||||||
| chr2:237995688 | G | C | 1 | a0001c0001t0007g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.214+879G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995688 | |||||||
| chr2:237995703 | T | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+894T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995703 | |||||||
| chr2:237995773 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(28): Show |
33 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.214+964A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995773 | |||||||
| chr2:237995776 | C | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+967C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995776 | |||||||
| chr2:237995849 | T | C | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+1040T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995849 | |||||||
| chr2:237995945 | A | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0110 a0001c0001t0001g0125 others(2): Show |
5 | HG00735.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+1136A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237995945 | |||||||
| chr2:237996001 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.214+1192A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996001 | |||||||
| chr2:237996024 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.214+1215G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996024 | |||||||
| chr2:237996150 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.214+1341G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996150 | |||||||
| chr2:237996173 | A | G | 1 | a0001c0001t0002g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214+1364A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996173 | |||||||
| chr2:237996221 | T | C | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+1412T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996221 | |||||||
| chr2:237996425 | T | C | 1 | a0001c0002t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.214+1616T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996425 | |||||||
| chr2:237996472 | CCG | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(24): Show |
30 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.214+1666_214+1667d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237996472 | ||||||
| chr2:237996473 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+1664C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996473 | |||||||
| chr2:237996475 | C | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.214+1666C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996475 | |||||||
| chr2:237996476 | G | GT | 10 | a0001c0001t0001g0223 a0001c0001t0001g0230 a0001c0001t0001g0237 others(7): Show |
10 | HG01081.hp2 HG01358.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+1683dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237996476 | ||||||
| chr2:237996476 | GT | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.214+1683delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237996476 | ||||||
| chr2:237996478 | T | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(24): Show |
30 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.214+1669T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996478 | |||||||
| chr2:237996543 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.214+1734C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996543 | |||||||
| chr2:237996601 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG00558.hp1 NA18948.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+1792G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996601 | |||||||
| chr2:237996656 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.214+1847A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996656 | |||||||
| chr2:237996864 | G | A | 1 | a0001c0001t0002g0334 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.214+2055G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996864 | |||||||
| chr2:237996895 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.214+2086A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237996895 | |||||||
| chr2:237997116 | A | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG00558.hp1 NA18948.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+2307A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997116 | |||||||
| chr2:237997273 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+2464T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997273 | |||||||
| chr2:237997274 | A | G | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.214+2465A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997274 | |||||||
| chr2:237997450 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.214+2641T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997450 | |||||||
| chr2:237997487 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.214+2678A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997487 | |||||||
| chr2:237997535 | A | G | 4 | a0001c0003t0001g0167 a0001c0003t0001g0168 a0001c0003t0001g0169 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2726A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997535 | |||||||
| chr2:237997581 | T | C | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.214+2772T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997581 | |||||||
| chr2:237997673 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(52): Show |
58 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.214+2864G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997673 | |||||||
| chr2:237997771 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+2962G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997771 | |||||||
| chr2:237997869 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+3060C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997869 | |||||||
| chr2:237997934 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.214+3125A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997934 | |||||||
| chr2:237997960 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.214+3151A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237997960 | |||||||
| chr2:237998142 | A | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+3333A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998142 | |||||||
| chr2:237998143 | T | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+3334T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998143 | |||||||
| chr2:237998314 | C | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+3505C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998314 | |||||||
| chr2:237998478 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.214+3669A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998478 | |||||||
| chr2:237998511 | AAT | A | 9 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+3705_214+3706d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237998511 | ||||||
| chr2:237998516 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.214+3707G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998516 | |||||||
| chr2:237998612 | CT | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.214+3819delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237998612 | ||||||
| chr2:237998619 | T | C | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+3810T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998619 | |||||||
| chr2:237998627 | T | A | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+3818T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998627 | |||||||
| chr2:237998684 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.214+3875A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998684 | |||||||
| chr2:237998717 | C | G | 1 | a0001c0002t0001g0149 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.214+3908C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237998717 | |||||||
| chr2:237999000 | A | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+4191A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999000 | |||||||
| chr2:237999088 | A | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(42): Show |
50 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.214+4279A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999088 | |||||||
| chr2:237999092 | T | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.214+4283T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999092 | |||||||
| chr2:237999093 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.214+4284T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999093 | |||||||
| chr2:237999096 | T | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.214+4287T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999096 | |||||||
| chr2:237999097 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.214+4288T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999097 | |||||||
| chr2:237999113 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+4304C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999113 | |||||||
| chr2:237999172 | TC | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+4366delC | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237999172 | ||||||
| chr2:237999356 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.214+4547C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999356 | |||||||
| chr2:237999365 | T | A | 1 | a0001c0001t0002g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.214+4556T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999365 | |||||||
| chr2:237999400 | T | A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+4591T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999400 | |||||||
| chr2:237999465 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+4656A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999465 | |||||||
| chr2:237999478 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+4669T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999478 | |||||||
| chr2:237999487 | T | C | 1 | a0001c0001t0007g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.214+4678T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999487 | |||||||
| chr2:237999719 | T | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
59 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(56): Show |
intron_variant | MODIFIER | c.214+4910T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999719 | |||||||
| chr2:237999739 | C | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0176 a0001c0001t0001g0178 others(18): Show |
21 | HG02074.hp2 HG02523.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.214+4930C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999739 | |||||||
| chr2:237999761 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.214+4952C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999761 | |||||||
| chr2:237999770 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.214+4961A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999770 | |||||||
| chr2:237999820 | C | CT | 13 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(10): Show |
13 | HG02055.hp2 HG02074.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.214+5033dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237999820 | ||||||
| chr2:237999820 | CTTTTTTT | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.214+5027_214+5033d others(9): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 237999820 | ||||||
| chr2:237999887 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.214+5078C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 237999887 | |||||||
| chr2:238000047 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5238C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000047 | |||||||
| chr2:238000062 | T | C | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+5253T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000062 | |||||||
| chr2:238000162 | T | C | 2 | a0001c0001t0003g0308 a0001c0001t0003g0309 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214+5353T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000162 | |||||||
| chr2:238000174 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.214+5365C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000174 | |||||||
| chr2:238000554 | C | T | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(124): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.214+5745C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000554 | |||||||
| chr2:238000613 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5804T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000613 | |||||||
| chr2:238000627 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+5818A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000627 | |||||||
| chr2:238000650 | T | G | 7 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+5841T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000650 | |||||||
| chr2:238000783 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+5974A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238000783 | |||||||
| chr2:238001033 | C | CT | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.214+6242dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238001033 | ||||||
| chr2:238001033 | C | CTT | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(73): Show |
83 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.214+6241_214+6242d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238001033 | ||||||
| chr2:238001128 | G | A | 1 | a0001c0001t0009g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.214+6319G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001128 | |||||||
| chr2:238001368 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.214+6559A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001368 | |||||||
| chr2:238001402 | T | G | 1 | a0001c0001t0002g0345 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+6593T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001402 | |||||||
| chr2:238001425 | G | T | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0060 others(123): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.214+6616G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001425 | |||||||
| chr2:238001474 | A | G | 1 | a0001c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.214+6665A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001474 | |||||||
| chr2:238001619 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.214+6810C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001619 | |||||||
| chr2:238001688 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214+6879C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001688 | |||||||
| chr2:238001797 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.214+6988G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001797 | |||||||
| chr2:238001936 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.214+7127G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238001936 | |||||||
| chr2:238002021 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+7212T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002021 | |||||||
| chr2:238002063 | A | ATT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
89 | HG00621.hp1 HG01169.hp2 HG01255.hp1 others(86): Show |
intron_variant | MODIFIER | c.214+7271_214+7272d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238002063 | ||||||
| chr2:238002063 | A | ATTT | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.214+7270_214+7272d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238002063 | ||||||
| chr2:238002063 | A | ATTTT | 18 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0073 others(15): Show |
18 | HG00642.hp1 HG01346.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+7269_214+7272d others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238002063 | ||||||
| chr2:238002231 | A | AT | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+7434dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238002231 | ||||||
| chr2:238002237 | T | TG | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.214+7428_214+7429i others(3): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002237 | |||||||
| chr2:238002253 | GTTTTGT | G | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+7466_214+7471d others(8): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238002253 | ||||||
| chr2:238002459 | C | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+7650C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002459 | |||||||
| chr2:238002653 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.214+7844C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002653 | |||||||
| chr2:238002715 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.214+7906G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002715 | |||||||
| chr2:238002935 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.214+8126G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002935 | |||||||
| chr2:238002974 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.214+8165A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238002974 | |||||||
| chr2:238003114 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+8305C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003114 | |||||||
| chr2:238003133 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | NA18943.hp1 NA18972.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+8324A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003133 | |||||||
| chr2:238003191 | G | GT | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
71 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.214+8393dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238003191 | ||||||
| chr2:238003329 | C | G | 1 | a0001c0002t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.214+8520C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003329 | |||||||
| chr2:238003348 | C | G | 1 | a0001c0002t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.214+8539C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003348 | |||||||
| chr2:238003361 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+8552T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003361 | |||||||
| chr2:238003478 | A | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+8669A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003478 | |||||||
| chr2:238003498 | T | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+8689T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003498 | |||||||
| chr2:238003504 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0229 a0001c0001t0001g0239 others(6): Show |
10 | HG01109.hp1 HG01928.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+8695C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003504 | |||||||
| chr2:238003505 | G | A | 1 | a0001c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.214+8696G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003505 | |||||||
| chr2:238003516 | A | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+8707A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003516 | |||||||
| chr2:238003701 | G | A | 1 | a0001c0001t0011g0280 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.214+8892G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003701 | |||||||
| chr2:238003804 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+8995A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003804 | |||||||
| chr2:238003836 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+9027G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003836 | |||||||
| chr2:238003984 | T | C | 25 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(22): Show |
25 | HG00140.hp2 HG00558.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.214+9175T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238003984 | |||||||
| chr2:238004248 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0011g0280 |
2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.214+9439T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238004248 | |||||||
| chr2:238004408 | G | GT | 7 | a0001c0001t0001g0061 a0001c0001t0003g0307 a0001c0001t0003g0308 others(4): Show |
7 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+9608dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238004408 | ||||||
| chr2:238004408 | GT | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0171 others(4): Show |
8 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+9608delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238004408 | ||||||
| chr2:238004602 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0196 a0001c0001t0001g0202 |
3 | NA18944.hp2 NA18961.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.214+9793C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238004602 | |||||||
| chr2:238004793 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.214+9984G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238004793 | |||||||
| chr2:238004959 | A | G | 5 | a0001c0001t0002g0014 a0001c0001t0002g0319 a0001c0001t0002g0321 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+10150A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238004959 | |||||||
| chr2:238005141 | G | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+10332G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005141 | |||||||
| chr2:238005153 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.214+10344G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005153 | |||||||
| chr2:238005188 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+10379T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005188 | |||||||
| chr2:238005255 | T | G | 3 | a0001c0003t0001g0168 a0001c0003t0001g0169 a0001c0003t0001g0170 |
3 | HG01891.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.214+10446T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005255 | |||||||
| chr2:238005451 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.214+10642C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005451 | |||||||
| chr2:238005537 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+10728T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005537 | |||||||
| chr2:238005538 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+10729G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005538 | |||||||
| chr2:238005603 | T | TG | 3 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0047 |
5 | HG02015.hp1 NA18945.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+10796dupG | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238005603 | ||||||
| chr2:238005605 | G | GT | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
186 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.214+10806dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238005605 | ||||||
| chr2:238005605 | G | GTT | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0060 others(96): Show |
101 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.214+10805_214+1080 others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238005605 | ||||||
| chr2:238005605 | G | GTTT | 28 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(25): Show |
28 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+10804_214+1080 others(7): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238005605 | ||||||
| chr2:238005660 | C | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+10851C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005660 | |||||||
| chr2:238005712 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.215-10854T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238005712 | |||||||
| chr2:238006154 | T | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-10412T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238006154 | |||||||
| chr2:238006164 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-10402G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238006164 | |||||||
| chr2:238006304 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.215-10262A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238006304 | |||||||
| chr2:238006405 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(53): Show |
59 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(56): Show |
intron_variant | MODIFIER | c.215-10161A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238006405 | |||||||
| chr2:238006725 | GGGACATC others(8): Show |
G | 1 | a0001c0001t0001g0069 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.215-9839_215-9825d others(17): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238006725 | ||||||
| chr2:238006759 | C | CT | 9 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0203 others(6): Show |
11 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-9790dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238006759 | ||||||
| chr2:238006759 | C | CTTTTTTT others(3): Show |
8 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0296 others(5): Show |
8 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-9799_215-9790d others(12): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238006759 | ||||||
| chr2:238006759 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.215-9800_215-9790d others(13): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238006759 | ||||||
| chr2:238006759 | CT | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(35): Show |
42 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(39): Show |
intron_variant | MODIFIER | c.215-9790delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238006759 | ||||||
| chr2:238006759 | CTT | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.215-9791_215-9790d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238006759 | ||||||
| chr2:238006767 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(24): Show |
30 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-9799T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238006767 | |||||||
| chr2:238006943 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-9623A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238006943 | |||||||
| chr2:238007086 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.215-9480C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007086 | |||||||
| chr2:238007115 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.215-9451C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007115 | |||||||
| chr2:238007210 | C | T | 1 | a0001c0001t0002g0340 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.215-9356C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007210 | |||||||
| chr2:238007301 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.215-9265T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007301 | |||||||
| chr2:238007519 | AT | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.215-9037delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238007519 | ||||||
| chr2:238007634 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-8932T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007634 | |||||||
| chr2:238007675 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-8891A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007675 | |||||||
| chr2:238007905 | G | T | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-8661G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238007905 | |||||||
| chr2:238008028 | A | G | 1 | a0001c0001t0002g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.215-8538A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008028 | |||||||
| chr2:238008106 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
195 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.215-8460G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008106 | |||||||
| chr2:238008145 | A | AT | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-8415dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238008145 | ||||||
| chr2:238008172 | A | G | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-8394A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008172 | |||||||
| chr2:238008237 | G | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.215-8329G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008237 | |||||||
| chr2:238008517 | T | C | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-8049T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008517 | |||||||
| chr2:238008809 | A | C | 1 | a0001c0001t0002g0293 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.215-7757A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008809 | |||||||
| chr2:238008899 | C | G | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-7667C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238008899 | |||||||
| chr2:238009081 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.215-7485T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238009081 | |||||||
| chr2:238009087 | C | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.215-7479C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238009087 | |||||||
| chr2:238009409 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0124 a0001c0002t0001g0144 |
3 | NA18953.hp1 NA18968.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.215-7157C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238009409 | |||||||
| chr2:238009419 | C | T | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.215-7147C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238009419 | |||||||
| chr2:238009612 | A | G | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-6954A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238009612 | |||||||
| chr2:238009971 | T | C | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-6595T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238009971 | |||||||
| chr2:238010150 | GTAGA | G | 14 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(11): Show |
14 | HG00621.hp1 HG02071.hp1 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-6406_215-6403d others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238010150 | ||||||
| chr2:238010182 | T | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | NA18944.hp1 NA18955.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-6384T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010182 | |||||||
| chr2:238010191 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.215-6375C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010191 | |||||||
| chr2:238010214 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-6352C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010214 | |||||||
| chr2:238010333 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(24): Show |
30 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-6233C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010333 | |||||||
| chr2:238010479 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.215-6087A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010479 | |||||||
| chr2:238010497 | A | G | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-6069A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010497 | |||||||
| chr2:238010564 | G | A | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-6002G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238010564 | |||||||
| chr2:238011092 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.215-5474C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011092 | |||||||
| chr2:238011123 | G | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-5443G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011123 | |||||||
| chr2:238011429 | C | T | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-5137C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011429 | |||||||
| chr2:238011489 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0118 |
2 | HG00140.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.215-5077G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011489 | |||||||
| chr2:238011490 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.215-5076C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011490 | |||||||
| chr2:238011713 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02165.hp1 NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.215-4853C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011713 | |||||||
| chr2:238011727 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.215-4839C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011727 | |||||||
| chr2:238011814 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-4752A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238011814 | |||||||
| chr2:238012044 | A | AT | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.215-4504dupT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238012044 | ||||||
| chr2:238012044 | A | ATT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(22): Show |
26 | HG00438.hp2 HG01255.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.215-4505_215-4504d others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238012044 | ||||||
| chr2:238012058 | T | C | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-4508T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012058 | |||||||
| chr2:238012095 | G | C | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.215-4471G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012095 | |||||||
| chr2:238012306 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
64 | HG00423.hp1 HG00621.hp1 HG01358.hp1 others(61): Show |
intron_variant | MODIFIER | c.215-4260G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012306 | |||||||
| chr2:238012336 | A | G | 1 | a0001c0002t0001g0207 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.215-4230A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012336 | |||||||
| chr2:238012340 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-4226G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012340 | |||||||
| chr2:238012346 | C | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0278 |
2 | HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.215-4220C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012346 | |||||||
| chr2:238012425 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-4141G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012425 | |||||||
| chr2:238012511 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.215-4055T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012511 | |||||||
| chr2:238012761 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.215-3805T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012761 | |||||||
| chr2:238012772 | G | A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-3794G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012772 | |||||||
| chr2:238012879 | A | G | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-3687A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238012879 | |||||||
| chr2:238013122 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.215-3444T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013122 | |||||||
| chr2:238013125 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.215-3441C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013125 | |||||||
| chr2:238013130 | C | T | 1 | a0001c0001t0007g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-3436C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013130 | |||||||
| chr2:238013203 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.215-3363G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013203 | |||||||
| chr2:238013517 | GT | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(123): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.215-3047delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238013517 | ||||||
| chr2:238013659 | G | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-2907G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013659 | |||||||
| chr2:238013693 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.215-2873G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013693 | |||||||
| chr2:238013943 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.215-2623G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238013943 | |||||||
| chr2:238014024 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.215-2542C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238014024 | |||||||
| chr2:238014213 | G | A | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-2353G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238014213 | |||||||
| chr2:238014336 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.215-2230A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238014336 | |||||||
| chr2:238014688 | T | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1878T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238014688 | |||||||
| chr2:238014760 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.215-1806A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238014760 | |||||||
| chr2:238014977 | T | G | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1589T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238014977 | |||||||
| chr2:238015003 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.215-1563C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238015003 | |||||||
| chr2:238015591 | AT | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.215-966delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 238015591 | ||||||
| chr2:238015722 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.215-844G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238015722 | |||||||
| chr2:238015862 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.215-704G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238015862 | |||||||
| chr2:238015915 | G | A | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(124): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.215-651G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238015915 | |||||||
| chr2:238015926 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.215-640G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238015926 | |||||||
| chr2:238016128 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(79): Show |
90 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.215-438C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238016128 | |||||||
| chr2:238016287 | A | G | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(6): Show |
9 | HG00621.hp1 NA18943.hp1 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-279A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238016287 | |||||||
| chr2:238016323 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(6): Show |
9 | HG00621.hp1 NA18943.hp1 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-243G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238016323 | |||||||
| chr2:238016365 | A | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0318 |
3 | HG00738.hp2 HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.215-201A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238016365 | |||||||
| chr2:238016410 | T | C | 1 | a0001c0001t0002g0345 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.215-156T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 4/9 | chr2 | 238016410 | |||||||
| chr2:238016819 | TC | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+188delC | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238016819 | ||||||
| chr2:238016822 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.282+189G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238016822 | |||||||
| chr2:238016831 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+198G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238016831 | |||||||
| chr2:238016842 | T | G | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+209T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238016842 | |||||||
| chr2:238016974 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
64 | HG00423.hp1 HG00621.hp1 HG01358.hp1 others(61): Show |
intron_variant | MODIFIER | c.282+341A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238016974 | |||||||
| chr2:238016987 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.282+354G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238016987 | |||||||
| chr2:238017013 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.282+380T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017013 | |||||||
| chr2:238017185 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0281 |
2 | HG01516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.282+552A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017185 | |||||||
| chr2:238017374 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+741A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017374 | |||||||
| chr2:238017412 | G | A | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+779G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017412 | |||||||
| chr2:238017597 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.282+964G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017597 | |||||||
| chr2:238017616 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.282+983G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017616 | |||||||
| chr2:238017711 | A | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+1078A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017711 | |||||||
| chr2:238017742 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.282+1109G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017742 | |||||||
| chr2:238017827 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.282+1194T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017827 | |||||||
| chr2:238017830 | T | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.282+1197T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017830 | |||||||
| chr2:238017860 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.282+1227C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017860 | |||||||
| chr2:238017965 | T | G | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.282+1332T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017965 | |||||||
| chr2:238017982 | C | T | 3 | a0001c0003t0001g0168 a0001c0003t0001g0169 a0001c0003t0001g0170 |
3 | HG01891.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.282+1349C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238017982 | |||||||
| chr2:238018312 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+1679C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018312 | |||||||
| chr2:238018342 | C | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+1709C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018342 | |||||||
| chr2:238018392 | TTTCAGGT others(3): Show |
T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+1761_282+1770d others(12): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238018392 | ||||||
| chr2:238018405 | T | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+1772T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018405 | |||||||
| chr2:238018441 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(25): Show |
31 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.282+1808A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018441 | |||||||
| chr2:238018521 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.282+1888C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018521 | |||||||
| chr2:238018589 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282+1956G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018589 | |||||||
| chr2:238018636 | G | C | 1 | a0001c0001t0001g0305 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.282+2003G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018636 | |||||||
| chr2:238018659 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+2026G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018659 | |||||||
| chr2:238018686 | C | T | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.282+2053C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018686 | |||||||
| chr2:238018973 | T | G | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.282+2340T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238018973 | |||||||
| chr2:238019654 | C | CTTT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0222 others(19): Show |
25 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.282+3038_282+3040d others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238019654 | ||||||
| chr2:238019654 | C | CTTTT | 50 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
54 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.282+3037_282+3040d others(6): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238019654 | ||||||
| chr2:238019654 | C | CTTTTT | 15 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0069 others(12): Show |
15 | HG00323.hp1 HG00733.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+3036_282+3040d others(7): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238019654 | ||||||
| chr2:238019654 | C | CTTTTTT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.282+3035_282+3040d others(8): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238019654 | ||||||
| chr2:238019654 | C | CTTTTTTT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(25): Show |
31 | HG00423.hp1 HG00438.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.282+3034_282+3040d others(9): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238019654 | ||||||
| chr2:238019729 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+3096A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238019729 | |||||||
| chr2:238019775 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+3142T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238019775 | |||||||
| chr2:238019821 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.282+3188G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238019821 | |||||||
| chr2:238019848 | C | T | 2 | a0001c0002t0001g0123 a0001c0002t0001g0162 |
2 | NA18991.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.282+3215C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238019848 | |||||||
| chr2:238019898 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.282+3265G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238019898 | |||||||
| chr2:238019943 | G | A | 1 | a0001c0002t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.282+3310G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238019943 | |||||||
| chr2:238020144 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(28): Show |
34 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.282+3511A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020144 | |||||||
| chr2:238020211 | C | T | 1 | a0001c0002t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.282+3578C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020211 | |||||||
| chr2:238020222 | C | T | 3 | a0001c0001t0001g0284 a0001c0001t0002g0322 a0001c0001t0002g0332 |
3 | HG00735.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.282+3589C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020222 | |||||||
| chr2:238020233 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+3600T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020233 | |||||||
| chr2:238020262 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.282+3629A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020262 | |||||||
| chr2:238020417 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.282+3784C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020417 | |||||||
| chr2:238020558 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.282+3925G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020558 | |||||||
| chr2:238020708 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.282+4075T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020708 | |||||||
| chr2:238020825 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+4192G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020825 | |||||||
| chr2:238020939 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+4306C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020939 | |||||||
| chr2:238020957 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0267 |
2 | HG01175.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.282+4324G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020957 | |||||||
| chr2:238020970 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
14 | HG01346.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.282+4337G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238020970 | |||||||
| chr2:238021068 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.283-4274C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021068 | |||||||
| chr2:238021291 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.283-4051G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021291 | |||||||
| chr2:238021419 | C | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0087 others(12): Show |
16 | HG00597.hp1 HG02071.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-3923C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021419 | |||||||
| chr2:238021488 | A | G | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-3854A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021488 | |||||||
| chr2:238021548 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283-3794G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021548 | |||||||
| chr2:238021721 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-3621G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021721 | |||||||
| chr2:238021787 | A | C | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-3555A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021787 | |||||||
| chr2:238021854 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.283-3488A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021854 | |||||||
| chr2:238021990 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.283-3352A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238021990 | |||||||
| chr2:238022053 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
64 | HG00423.hp1 HG00621.hp1 HG01358.hp1 others(61): Show |
intron_variant | MODIFIER | c.283-3289G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022053 | |||||||
| chr2:238022163 | T | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.283-3179T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022163 | |||||||
| chr2:238022170 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.283-3172C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022170 | |||||||
| chr2:238022175 | C | CTTTTT | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-3160_283-3156d others(7): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022175 | ||||||
| chr2:238022175 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0214 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.283-3156_283-3155i others(14): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022175 | ||||||
| chr2:238022175 | C | CTTTTTTT others(6): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
25 | HG01258.hp2 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.283-3156_283-3155i others(15): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022175 | ||||||
| chr2:238022175 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0210 a0001c0001t0001g0219 |
3 | HG01255.hp1 HG01346.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.283-3156_283-3155i others(16): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022175 | ||||||
| chr2:238022175 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 |
4 | HG02647.hp1 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-3156_283-3155i others(18): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022175 | ||||||
| chr2:238022175 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0171 a0001c0003t0001g0169 a0001c0003t0001g0170 |
3 | HG01891.hp2 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.283-3156_283-3155i others(19): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022175 | ||||||
| chr2:238022179 | T | TTTC | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.283-3161_283-3160i others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 238022179 | ||||||
| chr2:238022315 | C | T | 1 | a0001c0001t0002g0330 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.283-3027C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022315 | |||||||
| chr2:238022503 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG02145.hp2 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2839G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022503 | |||||||
| chr2:238022591 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0176 a0001c0001t0001g0178 others(16): Show |
19 | HG02074.hp2 HG02523.hp1 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.283-2751G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022591 | |||||||
| chr2:238022843 | G | T | 6 | a0001c0001t0001g0086 a0001c0001t0001g0110 a0001c0001t0001g0125 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-2499G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022843 | |||||||
| chr2:238022917 | C | T | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-2425C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022917 | |||||||
| chr2:238022998 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.283-2344G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238022998 | |||||||
| chr2:238023029 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.283-2313T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023029 | |||||||
| chr2:238023207 | G | A | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-2135G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023207 | |||||||
| chr2:238023392 | T | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.283-1950T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023392 | |||||||
| chr2:238023403 | A | C | 7 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1939A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023403 | |||||||
| chr2:238023612 | A | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.283-1730A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023612 | |||||||
| chr2:238023748 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(73): Show |
83 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.283-1594G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023748 | |||||||
| chr2:238023770 | C | T | 16 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.283-1572C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023770 | |||||||
| chr2:238023821 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0171 |
2 | NA19065.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.283-1521G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023821 | |||||||
| chr2:238023874 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283-1468T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238023874 | |||||||
| chr2:238024453 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.283-889T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238024453 | |||||||
| chr2:238024503 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(24): Show |
30 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.283-839G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238024503 | |||||||
| chr2:238024583 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0002g0293 a0001c0001t0002g0294 others(18): Show |
22 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.283-759A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238024583 | |||||||
| chr2:238024607 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.283-735G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238024607 | |||||||
| chr2:238024670 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283-672C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238024670 | |||||||
| chr2:238024793 | C | G | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-549C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238024793 | |||||||
| chr2:238025075 | A | C | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(24): Show |
27 | HG00741.hp2 HG02027.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.283-267A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238025075 | |||||||
| chr2:238025101 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.283-241C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238025101 | |||||||
| chr2:238025251 | G | A | 4 | a0001c0001t0001g0008 a0001c0003t0001g0168 a0001c0003t0001g0169 others(1): Show |
5 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-91G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238025251 | |||||||
| chr2:238025279 | G | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
19 | HG01346.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.283-63G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 5/9 | chr2 | 238025279 | |||||||
| chr2:238025553 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.353+141C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238025553 | |||||||
| chr2:238025600 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.353+188C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238025600 | |||||||
| chr2:238025715 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0282 |
2 | NA18985.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.353+303C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238025715 | |||||||
| chr2:238025896 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.353+484G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238025896 | |||||||
| chr2:238025936 | C | T | 16 | a0001c0001t0001g0086 a0001c0001t0001g0103 a0001c0001t0001g0110 others(13): Show |
16 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.353+524C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238025936 | |||||||
| chr2:238026007 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.353+595A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026007 | |||||||
| chr2:238026041 | A | G | 2 | a0001c0001t0002g0331 a0001c0001t0003g0307 |
2 | HG03041.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.353+629A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026041 | |||||||
| chr2:238026050 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.353+638T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026050 | |||||||
| chr2:238026064 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.353+652C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026064 | |||||||
| chr2:238026085 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.353+673A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026085 | |||||||
| chr2:238026102 | T | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0281 |
2 | HG01516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.353+690T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026102 | |||||||
| chr2:238026148 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.353+736C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026148 | |||||||
| chr2:238026155 | G | A | 7 | a0001c0001t0001g0286 a0001c0001t0003g0307 a0001c0001t0003g0308 others(4): Show |
7 | HG00438.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.353+743G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026155 | |||||||
| chr2:238026171 | G | A | 1 | a0001c0001t0002g0345 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.353+759G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026171 | |||||||
| chr2:238026226 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.353+814C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026226 | |||||||
| chr2:238026494 | C | T | 2 | a0001c0001t0002g0329 a0001c0001t0002g0345 |
2 | HG01928.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.353+1082C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026494 | |||||||
| chr2:238026504 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+1092G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026504 | |||||||
| chr2:238026520 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.353+1108G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026520 | |||||||
| chr2:238026555 | T | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0086 others(31): Show |
35 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.353+1143T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026555 | |||||||
| chr2:238026558 | C | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0142 |
2 | HG00544.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.353+1146C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026558 | |||||||
| chr2:238026579 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.353+1167G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026579 | |||||||
| chr2:238026643 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.353+1231C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026643 | |||||||
| chr2:238026679 | C | T | 1 | a0001c0001t0002g0318 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.353+1267C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026679 | |||||||
| chr2:238026844 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.353+1432A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026844 | |||||||
| chr2:238026977 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+1565G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238026977 | |||||||
| chr2:238027102 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+1690G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027102 | |||||||
| chr2:238027208 | T | C | 1 | a0001c0003t0001g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.353+1796T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027208 | |||||||
| chr2:238027457 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0271 |
2 | NA18991.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.353+2045C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027457 | |||||||
| chr2:238027500 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.353+2088G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027500 | |||||||
| chr2:238027508 | G | A | 1 | a0001c0002t0001g0313 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.353+2096G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027508 | |||||||
| chr2:238027823 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.353+2411T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027823 | |||||||
| chr2:238027829 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.353+2417G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238027829 | |||||||
| chr2:238028023 | A | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-2533A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028023 | |||||||
| chr2:238028221 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.354-2335G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028221 | |||||||
| chr2:238028495 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2061A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028495 | |||||||
| chr2:238028570 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.354-1986G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028570 | |||||||
| chr2:238028602 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-1954G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028602 | |||||||
| chr2:238028696 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.354-1860C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028696 | |||||||
| chr2:238028872 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.354-1684A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028872 | |||||||
| chr2:238028907 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.354-1649C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238028907 | |||||||
| chr2:238028924 | CT | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.354-1626delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 238028924 | ||||||
| chr2:238029019 | T | G | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-1537T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029019 | |||||||
| chr2:238029163 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.354-1393T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029163 | |||||||
| chr2:238029278 | T | TA | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.354-1271dupA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 238029278 | ||||||
| chr2:238029285 | A | AAT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0112 others(6): Show |
10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.354-1271_354-1270i others(4): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029285 | |||||||
| chr2:238029286 | T | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0112 others(7): Show |
11 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.354-1270T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029286 | |||||||
| chr2:238029287 | A | T | 1 | a0001c0002t0001g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.354-1269A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029287 | |||||||
| chr2:238029326 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.354-1230C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029326 | |||||||
| chr2:238029363 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.354-1193C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029363 | |||||||
| chr2:238029364 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.354-1192G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029364 | |||||||
| chr2:238029371 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.354-1185G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029371 | |||||||
| chr2:238029389 | C | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.354-1167C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029389 | |||||||
| chr2:238029595 | CA | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(47): Show |
54 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.354-944delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 238029595 | ||||||
| chr2:238029595 | CAA | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.354-945_354-944del others(2): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 238029595 | ||||||
| chr2:238029698 | C | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
23 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.354-858C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029698 | |||||||
| chr2:238029847 | G | A | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-709G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029847 | |||||||
| chr2:238029908 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.354-648C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238029908 | |||||||
| chr2:238029947 | CTTTCT | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0086 others(29): Show |
33 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.354-605_354-601del others(5): Show |
UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 238029947 | ||||||
| chr2:238029951 | CT | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(194): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.354-592delT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 238029951 | ||||||
| chr2:238030006 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.354-550C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030006 | |||||||
| chr2:238030130 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.354-426T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030130 | |||||||
| chr2:238030214 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.354-342A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030214 | |||||||
| chr2:238030359 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.354-197G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030359 | |||||||
| chr2:238030383 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.354-173C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030383 | |||||||
| chr2:238030440 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.354-116G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030440 | |||||||
| chr2:238030501 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.354-55G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 6/9 | chr2 | 238030501 | |||||||
| chr2:238030680 | TC | T | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+70delC | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 238030680 | ||||||
| chr2:238030729 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
85 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.411+116C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238030729 | |||||||
| chr2:238030790 | G | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG01358.hp1 HG01993.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+177G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238030790 | |||||||
| chr2:238031103 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411+490A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031103 | |||||||
| chr2:238031199 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.411+586C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031199 | |||||||
| chr2:238031246 | T | C | 1 | a0001c0002t0001g0292 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.411+633T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031246 | |||||||
| chr2:238031362 | C | T | 1 | a0001c0001t0002g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411+749C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031362 | |||||||
| chr2:238031393 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.411+780C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031393 | |||||||
| chr2:238031478 | T | C | 2 | a0001c0001t0001g0025 a0001c0003t0001g0211 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.412-744T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031478 | |||||||
| chr2:238031479 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(17): Show |
22 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.412-743C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031479 | |||||||
| chr2:238031611 | T | G | 3 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 |
3 | HG01081.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.412-611T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031611 | |||||||
| chr2:238031940 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.412-282G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 7/9 | chr2 | 238031940 | |||||||
| chr2:238032279 | A | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | NA18944.hp1 NA18955.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+25A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032279 | |||||||
| chr2:238032451 | C | CA | 9 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+203dupA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 238032451 | ||||||
| chr2:238032635 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.444+381C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032635 | |||||||
| chr2:238032687 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.444+433G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032687 | |||||||
| chr2:238032688 | T | A | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.444+434T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032688 | |||||||
| chr2:238032743 | G | A | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+489G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032743 | |||||||
| chr2:238032799 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.444+545G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032799 | |||||||
| chr2:238032900 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.444+646G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032900 | |||||||
| chr2:238032992 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(52): Show |
58 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.444+738T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238032992 | |||||||
| chr2:238033083 | G | T | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.444+829G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033083 | |||||||
| chr2:238033106 | G | T | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+852G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033106 | |||||||
| chr2:238033120 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.444+866G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033120 | |||||||
| chr2:238033159 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.444+905A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033159 | |||||||
| chr2:238033264 | A | G | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(124): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.444+1010A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033264 | |||||||
| chr2:238033323 | C | T | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+1069C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033323 | |||||||
| chr2:238033471 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.444+1217G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033471 | |||||||
| chr2:238033540 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+1286C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033540 | |||||||
| chr2:238033674 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.444+1420A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033674 | |||||||
| chr2:238033743 | C | T | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.444+1489C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033743 | |||||||
| chr2:238033833 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.444+1579G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033833 | |||||||
| chr2:238033932 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.444+1678G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238033932 | |||||||
| chr2:238034010 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.444+1756A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034010 | |||||||
| chr2:238034045 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.444+1791C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034045 | |||||||
| chr2:238034127 | TA | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1741delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 238034127 | ||||||
| chr2:238034151 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.445-1727G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034151 | |||||||
| chr2:238034184 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.445-1694G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034184 | |||||||
| chr2:238034200 | G | A | 10 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.445-1678G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034200 | |||||||
| chr2:238034238 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.445-1640A>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034238 | |||||||
| chr2:238034264 | T | TA | 7 | a0001c0001t0001g0093 a0001c0001t0003g0308 a0001c0001t0003g0309 others(4): Show |
7 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-1600dupA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 238034264 | ||||||
| chr2:238034264 | TA | T | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0133 others(3): Show |
6 | HG02135.hp2 HG02280.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1600delA | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 238034264 | ||||||
| chr2:238034415 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(23): Show |
29 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.445-1463C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034415 | |||||||
| chr2:238034439 | A | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0172 |
3 | HG02486.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.445-1439A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034439 | |||||||
| chr2:238034484 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0183 others(3): Show |
6 | NA18950.hp2 NA18952.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1394C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034484 | |||||||
| chr2:238034745 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG02145.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.445-1133C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034745 | |||||||
| chr2:238034837 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-1041C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034837 | |||||||
| chr2:238034840 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.445-1038C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034840 | |||||||
| chr2:238034863 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.445-1015T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238034863 | |||||||
| chr2:238035016 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.445-862C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035016 | |||||||
| chr2:238035172 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.445-706G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035172 | |||||||
| chr2:238035288 | C | T | 1 | a0001c0001t0009g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445-590C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035288 | |||||||
| chr2:238035325 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.445-553T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035325 | |||||||
| chr2:238035385 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.445-493G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035385 | |||||||
| chr2:238035586 | A | T | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-292A>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035586 | |||||||
| chr2:238035617 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(17): Show |
22 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.445-261A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035617 | |||||||
| chr2:238035633 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.445-245G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035633 | |||||||
| chr2:238035722 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.445-156G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035722 | |||||||
| chr2:238035800 | ACT | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
85 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-77_445-76delCT | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 8/9 | chr2 | 238035800 | |||||||
| chr2:238035976 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.507+36C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238035976 | |||||||
| chr2:238036081 | C | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+141C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036081 | |||||||
| chr2:238036154 | TG | T | 8 | a0001c0001t0002g0014 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
9 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+215delG | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036154 | |||||||
| chr2:238036175 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
85 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.507+235G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036175 | |||||||
| chr2:238036205 | C | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0319 a0001c0001t0002g0321 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+265C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036205 | |||||||
| chr2:238036213 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0013g0246 |
2 | HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.507+273C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036213 | |||||||
| chr2:238036279 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.507+339C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036279 | |||||||
| chr2:238036339 | A | G | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+399A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036339 | |||||||
| chr2:238036458 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.507+518G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036458 | |||||||
| chr2:238036480 | G | A | 6 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+540G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238036480 | |||||||
| chr2:238037053 | G | C | 1 | a0001c0001t0003g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.507+1113G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037053 | |||||||
| chr2:238037078 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.507+1138T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037078 | |||||||
| chr2:238037207 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.507+1267G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037207 | |||||||
| chr2:238037271 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(17): Show |
22 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.507+1331A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037271 | |||||||
| chr2:238037289 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.507+1349A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037289 | |||||||
| chr2:238037294 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.507+1354C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037294 | |||||||
| chr2:238037340 | G | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+1400G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037340 | |||||||
| chr2:238037378 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+1438A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037378 | |||||||
| chr2:238037438 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.507+1498G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037438 | |||||||
| chr2:238037632 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+1692G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037632 | |||||||
| chr2:238037748 | G | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.507+1808G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037748 | |||||||
| chr2:238037749 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(52): Show |
58 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.507+1809G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037749 | |||||||
| chr2:238037755 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
85 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.507+1815G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037755 | |||||||
| chr2:238037763 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.507+1823A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037763 | |||||||
| chr2:238037774 | T | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.507+1834T>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037774 | |||||||
| chr2:238037797 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.507+1857G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037797 | |||||||
| chr2:238037886 | C | T | 2 | a0001c0001t0002g0319 a0001c0001t0002g0323 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.507+1946C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037886 | |||||||
| chr2:238037942 | C | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+2002C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037942 | |||||||
| chr2:238037955 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+2015T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037955 | |||||||
| chr2:238037969 | C | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(23): Show |
29 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.507+2029C>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238037969 | |||||||
| chr2:238038057 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.507+2117T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038057 | |||||||
| chr2:238038174 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+2234C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038174 | |||||||
| chr2:238038185 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+2245T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038185 | |||||||
| chr2:238038222 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0003g0307 a0001c0001t0003g0308 others(4): Show |
7 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+2282G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038222 | |||||||
| chr2:238038257 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.507+2317A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038257 | |||||||
| chr2:238038313 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0003t0001g0167 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+2373T>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038313 | |||||||
| chr2:238038486 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.507+2546G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038486 | |||||||
| chr2:238038634 | T | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-2654T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038634 | |||||||
| chr2:238038972 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(21): Show |
27 | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.508-2316C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238038972 | |||||||
| chr2:238039006 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.508-2282A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039006 | |||||||
| chr2:238039061 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.508-2227C>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039061 | |||||||
| chr2:238039071 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(52): Show |
58 | HG00423.hp1 HG00621.hp1 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.508-2217G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039071 | |||||||
| chr2:238039086 | T | C | 1 | a0001c0002t0001g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.508-2202T>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039086 | |||||||
| chr2:238039092 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.508-2196G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039092 | |||||||
| chr2:238039150 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.508-2138A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039150 | |||||||
| chr2:238039191 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.508-2097C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039191 | |||||||
| chr2:238039223 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.508-2065G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039223 | |||||||
| chr2:238039310 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.508-1978G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039310 | |||||||
| chr2:238039330 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.508-1958G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039330 | |||||||
| chr2:238039341 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.508-1947G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039341 | |||||||
| chr2:238039809 | G | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG02027.hp2 HG02056.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-1479G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039809 | |||||||
| chr2:238039849 | A | G | 1 | a0001c0002t0001g0144 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.508-1439A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238039849 | |||||||
| chr2:238040116 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.508-1172G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040116 | |||||||
| chr2:238040226 | G | C | 2 | a0001c0002t0001g0097 a0001c0002t0001g0101 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.508-1062G>C | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040226 | |||||||
| chr2:238040281 | G | A | 7 | a0001c0001t0002g0346 a0001c0001t0003g0307 a0001c0001t0003g0308 others(4): Show |
7 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-1007G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040281 | |||||||
| chr2:238040668 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.508-620G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040668 | |||||||
| chr2:238040701 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.508-587G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040701 | |||||||
| chr2:238040709 | C | T | 5 | a0001c0001t0001g0008 a0001c0003t0001g0167 a0001c0003t0001g0168 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-579C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040709 | |||||||
| chr2:238040739 | A | G | 1 | a0001c0001t0002g0013 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.508-549A>G | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040739 | |||||||
| chr2:238040961 | G | A | 5 | a0001c0001t0003g0308 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-327G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040961 | |||||||
| chr2:238040969 | G | A | 1 | a0001c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-319G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040969 | |||||||
| chr2:238040975 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(21): Show |
27 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.508-313G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238040975 | |||||||
| chr2:238041053 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.508-235C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238041053 | |||||||
| chr2:238041102 | G | A | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(123): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.508-186G>A | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238041102 | |||||||
| chr2:238041151 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.508-137G>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238041151 | |||||||
| chr2:238041267 | C | T | 1 | a0001c0001t0002g0338 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.508-21C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238041267 | |||||||
| chr2:238041282 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.508-6C>T | UBE2F | ENSG00000184182.19 | transcript | ENST00000272930.9 | protein_coding | 9/9 | chr2 | 238041282 |