Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10477 |
| ensemblid | ENSG00000170035.16 |
| hgncid | 12479 |
| symbol | UBE2E3 |
| name | ubiquitin conjugating enzyme E2 E3 |
| refseq_nuc | NM_006357.4 |
| refseq_prot | NP_006348.1 |
| ensembl_nuc | ENST00000410062.9 |
| ensembl_prot | ENSP00000386788.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 180980605 |
| end | 181063425 |
| strand | + |
| ver | v1.2 |
| region | chr2:180980605-181063425 |
| region5000 | chr2:180975605-181068425 |
| regionname0 | UBE2E3_chr2_180980605_181063425 |
| regionname5000 | UBE2E3_chr2_180975605_181068425 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 207 | 337 | 96 | 58 | 123 | 16 | 42 | 94 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | MSSDR others(202): Show |
chr2 | 180975605 | 181068425 |
| a0002 | 0/0 | 207 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | MSSDR others(202): Show |
chr2 | 180975605 | 181068425 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 621 | 337 | 96 | 58 | 123 | 16 | 42 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | ATGTC others(616): Show |
chr2 | 180975605 | 181068425 | ||
| a0002c0002 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | ATGTC others(616): Show |
chr2 | 180975605 | 181068425 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1555 | 253 | 85 | 39 | 89 | 9 | 29 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1550): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0002 | 0/0 | 1558 | 37 | 0 | 11 | 14 | 7 | 5 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1553): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0003 | 0/0 | 1556 | 27 | 4 | 7 | 9 | 0 | 7 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1551): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0004 | 0/0 | 1558 | 6 | 0 | 0 | 6 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1553): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0005 | 0/0 | 1555 | 5 | 5 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1550): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0006 | 0/0 | 1559 | 2 | 0 | 1 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1554): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0007 | 0/0 | 1559 | 2 | 0 | 0 | 2 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1554): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0008 | 0/0 | 1555 | 2 | 1 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1550): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0009 | 0/0 | 1555 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1550): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0010 | 0/0 | 1555 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1550): Show |
chr2 | 180975605 | 181068425 |
| a0001c0001t0011 | 0/0 | 1556 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1551): Show |
chr2 | 180975605 | 181068425 |
| a0002c0002t0003 | 0/0 | 1556 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | GGAAC others(1551): Show |
chr2 | 180975605 | 181068425 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0001c0001t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0142 | EUR | GBR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | FIN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0163 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0140 | EUR | IBS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | IBS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0141 | EUR | IBS | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02135 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0121 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0035 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0243 | SAS | BEB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | STU | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0012 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19060 | hp2 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | ASW | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0321 | EUR | TSI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | USA | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | USA | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0176 | REF | REF | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0100 | REF | REF | UBE2E3_chr2_180975605_181068425 | UBE2E3 | chr2 | 180975605 | 181068425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:180982233 | A | G | 1 | a0002 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.191A>G | p.Lys64Arg | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/6 | 585/1555 | 191/624 | 64/207 | chr2 | 180982233 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:180980642 | G | GGGC | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(1): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-345_-343dupCGG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/6 | 1386 | INFO_REALIGN_3_PRIME | chr2 | 180980642 | |||||
| chr2:180980693 | C | A | 1 | a0001c0001t0009 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-306C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/6 | 1350 | chr2 | 180980693 | ||||||
| chr2:180980701 | C | T | 2 | a0001c0001t0005 a0001c0001t0011 |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-298C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/6 | chr2 | 180980701 | |||||||
| chr2:180980872 | T | C | 1 | a0001c0001t0008 | 2 | HG02055.hp2 NA19090.hp2 |
5_prime_UTR_variant | MODIFIER | c.-127T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/6 | 1171 | chr2 | 180980872 | ||||||
| chr2:180980872 | T | TC | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(2): Show |
33 | HG00741.hp2 HG01175.hp1 HG01243.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-118dupC | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/6 | 1161 | INFO_REALIGN_3_PRIME | chr2 | 180980872 | |||||
| chr2:180980882 | A | C | 2 | a0001c0001t0004 a0001c0001t0007 |
8 | NA18951.hp1 NA18954.hp2 NA18964.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-117A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/6 | 1161 | chr2 | 180980882 | ||||||
| chr2:181063047 | T | C | 1 | a0001c0001t0010 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 6/6 | 159 | chr2 | 181063047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:180981067 | G | A | 1 | a0001c0001t0010g0012 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-26+94G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/5 | chr2 | 180981067 | |||||||
| chr2:180981106 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-26+133C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/5 | chr2 | 180981106 | |||||||
| chr2:180981177 | C | G | 1 | a0001c0001t0003g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-26+204C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/5 | chr2 | 180981177 | |||||||
| chr2:180981197 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26+224G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/5 | chr2 | 180981197 | |||||||
| chr2:180981867 | TGTAC | T | 44 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.-25-146_-25-143del others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 180981867 | ||||||
| chr2:180981966 | T | G | 1 | a0001c0001t0002g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-25-52T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 1/5 | chr2 | 180981966 | |||||||
| chr2:180982494 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.194+258T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | chr2 | 180982494 | |||||||
| chr2:180982580 | ATCT | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0324 |
3 | HG01891.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.194+349_194+351del others(3): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 180982580 | ||||||
| chr2:180982678 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.194+442A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | chr2 | 180982678 | |||||||
| chr2:180982896 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.194+660C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | chr2 | 180982896 | |||||||
| chr2:180982942 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.194+706A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | chr2 | 180982942 | |||||||
| chr2:180983048 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.194+812T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | chr2 | 180983048 | |||||||
| chr2:180984026 | T | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.195-17T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 2/5 | chr2 | 180984026 | |||||||
| chr2:180984220 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.245+127A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180984220 | |||||||
| chr2:180984384 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.245+291A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180984384 | |||||||
| chr2:180985099 | C | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+1006C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985099 | |||||||
| chr2:180985157 | C | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+1064C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985157 | |||||||
| chr2:180985261 | A | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+1168A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985261 | |||||||
| chr2:180985375 | T | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG00558.hp1 HG02074.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.245+1282T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985375 | |||||||
| chr2:180985405 | A | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG01074.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.245+1312A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985405 | |||||||
| chr2:180985542 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+1449G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985542 | |||||||
| chr2:180985566 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+1473A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985566 | |||||||
| chr2:180985599 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+1506G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985599 | |||||||
| chr2:180985885 | CAG | C | 9 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+1795_245+1796d others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180985885 | ||||||
| chr2:180985892 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+1799A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985892 | |||||||
| chr2:180985951 | TC | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+1860delC | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180985951 | ||||||
| chr2:180985986 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.245+1893A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985986 | |||||||
| chr2:180985997 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+1904A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180985997 | |||||||
| chr2:180986004 | A | C | 47 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0024 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.245+1911A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986004 | |||||||
| chr2:180986069 | C | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(6): Show |
10 | HG02615.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.245+1976C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986069 | |||||||
| chr2:180986202 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.245+2109G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986202 | |||||||
| chr2:180986374 | G | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.245+2281G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986374 | |||||||
| chr2:180986376 | G | T | 1 | a0001c0001t0002g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.245+2283G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986376 | |||||||
| chr2:180986450 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.245+2357C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986450 | |||||||
| chr2:180986563 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245+2470G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986563 | |||||||
| chr2:180986605 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+2512A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180986605 | |||||||
| chr2:180987051 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+2958C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180987051 | |||||||
| chr2:180987172 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+3079G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180987172 | |||||||
| chr2:180987236 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+3143A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180987236 | |||||||
| chr2:180987269 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+3176T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180987269 | |||||||
| chr2:180987270 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+3177T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180987270 | |||||||
| chr2:180987849 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245+3756G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180987849 | |||||||
| chr2:180988037 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245+3944C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988037 | |||||||
| chr2:180988215 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245+4122C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988215 | |||||||
| chr2:180988301 | A | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.245+4208A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988301 | |||||||
| chr2:180988368 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.245+4275G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988368 | |||||||
| chr2:180988418 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+4325T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988418 | |||||||
| chr2:180988424 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.245+4331T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988424 | |||||||
| chr2:180988450 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+4357T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988450 | |||||||
| chr2:180988630 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.245+4537C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988630 | |||||||
| chr2:180988651 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+4558C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988651 | |||||||
| chr2:180988673 | A | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.245+4580A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988673 | |||||||
| chr2:180988768 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.245+4675T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988768 | |||||||
| chr2:180988916 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+4823G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988916 | |||||||
| chr2:180988934 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+4841T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180988934 | |||||||
| chr2:180989049 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.245+4956G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989049 | |||||||
| chr2:180989052 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.245+4959T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989052 | |||||||
| chr2:180989170 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(11): Show |
15 | HG01081.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.245+5077A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989170 | |||||||
| chr2:180989191 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+5098C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989191 | |||||||
| chr2:180989255 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0006g0022 |
2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.245+5162T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989255 | |||||||
| chr2:180989273 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00642.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.245+5180G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989273 | |||||||
| chr2:180989373 | G | T | 1 | a0001c0001t0002g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.245+5280G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989373 | |||||||
| chr2:180989620 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245+5527A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989620 | |||||||
| chr2:180989916 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | NA18959.hp1 NA18961.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+5823A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989916 | |||||||
| chr2:180989965 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+5872C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989965 | |||||||
| chr2:180989982 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245+5889A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180989982 | |||||||
| chr2:180990038 | C | T | 1 | a0001c0001t0002g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.245+5945C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990038 | |||||||
| chr2:180990257 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245+6164A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990257 | |||||||
| chr2:180990270 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+6177C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990270 | |||||||
| chr2:180990270 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.245+6177C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990270 | |||||||
| chr2:180990276 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+6183T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990276 | |||||||
| chr2:180990278 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+6185G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990278 | |||||||
| chr2:180990434 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
30 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.245+6341T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990434 | |||||||
| chr2:180990437 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
30 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.245+6344T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990437 | |||||||
| chr2:180990441 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.245+6348T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990441 | |||||||
| chr2:180990492 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+6399C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990492 | |||||||
| chr2:180990566 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+6473A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990566 | |||||||
| chr2:180990687 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.245+6594G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990687 | |||||||
| chr2:180990735 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.245+6642C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990735 | |||||||
| chr2:180990805 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.245+6712G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990805 | |||||||
| chr2:180990889 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.245+6796A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990889 | |||||||
| chr2:180990938 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+6845G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180990938 | |||||||
| chr2:180991059 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.245+6966A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991059 | |||||||
| chr2:180991096 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7003C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991096 | |||||||
| chr2:180991149 | A | AT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(118): Show |
124 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.245+7065dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180991149 | ||||||
| chr2:180991149 | A | ATT | 13 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(10): Show |
13 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.245+7064_245+7065d others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180991149 | ||||||
| chr2:180991149 | A | ATTT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.245+7063_245+7065d others(5): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180991149 | ||||||
| chr2:180991159 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.245+7066C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991159 | |||||||
| chr2:180991200 | C | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+7107C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991200 | |||||||
| chr2:180991213 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7120C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991213 | |||||||
| chr2:180991237 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+7144G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991237 | |||||||
| chr2:180991304 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7211T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991304 | |||||||
| chr2:180991333 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7240C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991333 | |||||||
| chr2:180991368 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245+7275A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991368 | |||||||
| chr2:180991369 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245+7276G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991369 | |||||||
| chr2:180991370 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245+7277A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991370 | |||||||
| chr2:180991395 | C | G | 1 | a0001c0001t0002g0053 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.245+7302C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991395 | |||||||
| chr2:180991405 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+7312G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991405 | |||||||
| chr2:180991481 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+7388A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991481 | |||||||
| chr2:180991568 | C | G | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+7475C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991568 | |||||||
| chr2:180991630 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7537G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991630 | |||||||
| chr2:180991719 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7626T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180991719 | |||||||
| chr2:180991824 | T | TG | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7733dupG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180991824 | ||||||
| chr2:180992021 | G | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.245+7928G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992021 | |||||||
| chr2:180992056 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+7963C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992056 | |||||||
| chr2:180992133 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.245+8040G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992133 | |||||||
| chr2:180992142 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.245+8049C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992142 | |||||||
| chr2:180992258 | CTT | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.245+8168_245+8169d others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180992258 | ||||||
| chr2:180992321 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+8228T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992321 | |||||||
| chr2:180992539 | CTG | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+8450_245+8451d others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180992539 | ||||||
| chr2:180992552 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.245+8459T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992552 | |||||||
| chr2:180992565 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+8472T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992565 | |||||||
| chr2:180992657 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+8564G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992657 | |||||||
| chr2:180992661 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+8568A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992661 | |||||||
| chr2:180992665 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+8572T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992665 | |||||||
| chr2:180992668 | T | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.245+8575T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992668 | |||||||
| chr2:180992786 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+8693C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992786 | |||||||
| chr2:180992835 | AT | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+8752delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180992835 | ||||||
| chr2:180992896 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+8803A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992896 | |||||||
| chr2:180992953 | A | G | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG02083.hp2 NA18975.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.245+8860A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180992953 | |||||||
| chr2:180993236 | C | G | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.245+9143C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993236 | |||||||
| chr2:180993267 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245+9174A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993267 | |||||||
| chr2:180993441 | G | C | 37 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0063 others(34): Show |
37 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.245+9348G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993441 | |||||||
| chr2:180993442 | T | C | 47 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0024 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.245+9349T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993442 | |||||||
| chr2:180993578 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+9485C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993578 | |||||||
| chr2:180993586 | T | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+9493T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993586 | |||||||
| chr2:180993621 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+9528T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993621 | |||||||
| chr2:180993725 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+9632C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993725 | |||||||
| chr2:180993766 | A | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+9673A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993766 | |||||||
| chr2:180993803 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02630.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.245+9710G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993803 | |||||||
| chr2:180993884 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+9791T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993884 | |||||||
| chr2:180993885 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+9792A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180993885 | |||||||
| chr2:180994015 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.245+9922C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994015 | |||||||
| chr2:180994617 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245+10524A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994617 | |||||||
| chr2:180994833 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+10740G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994833 | |||||||
| chr2:180994929 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.245+10836A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994929 | |||||||
| chr2:180994937 | T | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.245+10844T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994937 | |||||||
| chr2:180994975 | A | G | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+10882A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994975 | |||||||
| chr2:180994996 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
9 | HG01168.hp1 HG01169.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+10903G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180994996 | |||||||
| chr2:180995218 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.245+11125C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180995218 | |||||||
| chr2:180995280 | G | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.245+11187G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180995280 | |||||||
| chr2:180995440 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.245+11347A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180995440 | |||||||
| chr2:180995471 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+11378T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180995471 | |||||||
| chr2:180995739 | A | AT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0092 a0001c0001t0001g0128 others(15): Show |
19 | HG01081.hp2 HG01884.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.245+11661dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180995739 | ||||||
| chr2:180996054 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245+11961A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996054 | |||||||
| chr2:180996094 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+12001A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996094 | |||||||
| chr2:180996121 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.245+12028T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996121 | |||||||
| chr2:180996161 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.245+12068A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996161 | |||||||
| chr2:180996357 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+12264T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996357 | |||||||
| chr2:180996496 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+12403T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996496 | |||||||
| chr2:180996576 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.245+12483A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996576 | |||||||
| chr2:180996586 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.245+12493A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996586 | |||||||
| chr2:180996914 | C | T | 1 | a0001c0001t0003g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245+12821C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180996914 | |||||||
| chr2:180997016 | T | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+12923T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997016 | |||||||
| chr2:180997111 | C | CT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+13029dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180997111 | ||||||
| chr2:180997241 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+13148C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997241 | |||||||
| chr2:180997249 | A | C | 1 | a0001c0001t0005g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.245+13156A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997249 | |||||||
| chr2:180997252 | T | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | NA19063.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.245+13159T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997252 | |||||||
| chr2:180997371 | C | T | 1 | a0001c0001t0003g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245+13278C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997371 | |||||||
| chr2:180997408 | G | A | 10 | a0001c0001t0001g0059 a0001c0001t0001g0127 a0001c0001t0001g0184 others(7): Show |
10 | HG01175.hp1 HG02015.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.245+13315G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997408 | |||||||
| chr2:180997436 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+13343C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997436 | |||||||
| chr2:180997441 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.245+13348T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997441 | |||||||
| chr2:180997521 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+13428C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997521 | |||||||
| chr2:180997532 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+13439T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997532 | |||||||
| chr2:180997561 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.245+13468C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997561 | |||||||
| chr2:180997740 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.245+13647A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997740 | |||||||
| chr2:180997760 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(21): Show |
28 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+13667G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997760 | |||||||
| chr2:180997794 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+13701C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997794 | |||||||
| chr2:180997798 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245+13705G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997798 | |||||||
| chr2:180997852 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.245+13759G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997852 | |||||||
| chr2:180997890 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0301 a0001c0001t0001g0302 |
4 | HG01884.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+13797C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997890 | |||||||
| chr2:180997948 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.245+13855T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180997948 | |||||||
| chr2:180998082 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.245+13989C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998082 | |||||||
| chr2:180998339 | A | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+14246A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998339 | |||||||
| chr2:180998401 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+14308G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998401 | |||||||
| chr2:180998458 | T | TTGGGATA others(29): Show |
1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245+14365_245+1436 others(40): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998458 | |||||||
| chr2:180998461 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245+14368G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998461 | |||||||
| chr2:180998461 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245+14368G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998461 | |||||||
| chr2:180998494 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+14401A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998494 | |||||||
| chr2:180998537 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+14444T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998537 | |||||||
| chr2:180998551 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+14458T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998551 | |||||||
| chr2:180998559 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+14466A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998559 | |||||||
| chr2:180998625 | T | C | 47 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0024 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.245+14532T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998625 | |||||||
| chr2:180998689 | A | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0251 |
3 | NA18954.hp1 NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.245+14596A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998689 | |||||||
| chr2:180998751 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.245+14658C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180998751 | |||||||
| chr2:180999016 | C | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.245+14923C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999016 | |||||||
| chr2:180999065 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.245+14972A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999065 | |||||||
| chr2:180999091 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.245+14998C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999091 | |||||||
| chr2:180999160 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(21): Show |
28 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+15067G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999160 | |||||||
| chr2:180999160 | G | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.245+15067G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999160 | |||||||
| chr2:180999173 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+15080A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999173 | |||||||
| chr2:180999202 | G | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+15109G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999202 | |||||||
| chr2:180999216 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+15123C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999216 | |||||||
| chr2:180999319 | A | G | 1 | a0001c0001t0004g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.245+15226A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999319 | |||||||
| chr2:180999338 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245+15245G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999338 | |||||||
| chr2:180999339 | T | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0003g0251 |
3 | NA18954.hp1 NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.245+15246T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999339 | |||||||
| chr2:180999350 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+15257T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999350 | |||||||
| chr2:180999595 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.245+15502T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999595 | |||||||
| chr2:180999601 | G | GT | 15 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(12): Show |
16 | HG01081.hp2 HG01884.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.245+15516dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180999601 | ||||||
| chr2:180999690 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
30 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.245+15597A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999690 | |||||||
| chr2:180999790 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.245+15697A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999790 | |||||||
| chr2:180999791 | T | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+15698T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999791 | |||||||
| chr2:180999902 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+15809G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 180999902 | |||||||
| chr2:180999909 | TAAACAGG others(1): Show |
T | 16 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(13): Show |
16 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.245+15818_245+1582 others(12): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 180999909 | ||||||
| chr2:181000119 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.245+16026T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000119 | |||||||
| chr2:181000125 | A | C | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245+16032A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000125 | |||||||
| chr2:181000229 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+16136G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000229 | |||||||
| chr2:181000288 | TAAA | T | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG00735.hp1 HG02055.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+16199_245+1620 others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181000288 | ||||||
| chr2:181000367 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+16274T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000367 | |||||||
| chr2:181000409 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.245+16316C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000409 | |||||||
| chr2:181000439 | G | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.245+16346G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000439 | |||||||
| chr2:181000451 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245+16358A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000451 | |||||||
| chr2:181000459 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+16366C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000459 | |||||||
| chr2:181000551 | A | T | 107 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0131 others(104): Show |
108 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.245+16458A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000551 | |||||||
| chr2:181000556 | C | CT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(33): Show |
40 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.245+16479dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181000556 | ||||||
| chr2:181000556 | CT | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.245+16479delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181000556 | ||||||
| chr2:181000587 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.245+16494C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000587 | |||||||
| chr2:181000603 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+16510G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000603 | |||||||
| chr2:181000684 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0293 others(13): Show |
17 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.245+16591A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000684 | |||||||
| chr2:181000756 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+16663G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000756 | |||||||
| chr2:181000789 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+16696T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000789 | |||||||
| chr2:181000876 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.245+16783C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000876 | |||||||
| chr2:181000999 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.245+16906A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181000999 | |||||||
| chr2:181001035 | A | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | HG01081.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+16942A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001035 | |||||||
| chr2:181001143 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+17050T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001143 | |||||||
| chr2:181001144 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0195 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.245+17051A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001144 | |||||||
| chr2:181001262 | T | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(122): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.245+17169T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001262 | |||||||
| chr2:181001347 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+17254G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001347 | |||||||
| chr2:181001407 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.245+17314G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001407 | |||||||
| chr2:181001408 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.245+17315C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001408 | |||||||
| chr2:181001510 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245+17417G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001510 | |||||||
| chr2:181001533 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.245+17440A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001533 | |||||||
| chr2:181001602 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.245+17509G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001602 | |||||||
| chr2:181001621 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+17528G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001621 | |||||||
| chr2:181001779 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+17686G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001779 | |||||||
| chr2:181001830 | T | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+17737T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001830 | |||||||
| chr2:181001883 | A | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+17790A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001883 | |||||||
| chr2:181001926 | C | T | 1 | a0001c0001t0003g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.245+17833C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001926 | |||||||
| chr2:181001973 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(11): Show |
15 | HG01081.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.245+17880T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181001973 | |||||||
| chr2:181002014 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+17921T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002014 | |||||||
| chr2:181002086 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.245+17993C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002086 | |||||||
| chr2:181002153 | T | C | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245+18060T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002153 | |||||||
| chr2:181002191 | CT | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+18105delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181002191 | ||||||
| chr2:181002230 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.245+18137G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002230 | |||||||
| chr2:181002247 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+18154C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002247 | |||||||
| chr2:181002248 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+18155A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002248 | |||||||
| chr2:181002320 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.245+18227G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002320 | |||||||
| chr2:181002398 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0324 |
3 | HG01891.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.245+18305T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002398 | |||||||
| chr2:181002458 | T | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
213 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.245+18365T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002458 | |||||||
| chr2:181002465 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245+18372G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002465 | |||||||
| chr2:181002597 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+18504A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002597 | |||||||
| chr2:181002621 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.245+18528A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002621 | |||||||
| chr2:181002652 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+18559A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002652 | |||||||
| chr2:181002667 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245+18574C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002667 | |||||||
| chr2:181002718 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245+18625C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002718 | |||||||
| chr2:181002748 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.245+18655G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002748 | |||||||
| chr2:181002807 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+18714C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002807 | |||||||
| chr2:181002810 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.245+18717C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002810 | |||||||
| chr2:181002886 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18962.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.245+18793A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181002886 | |||||||
| chr2:181003074 | C | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(19): Show |
25 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.245+18981C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003074 | |||||||
| chr2:181003113 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0301 a0001c0001t0001g0302 |
4 | HG01884.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+19020C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003113 | |||||||
| chr2:181003117 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19024T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003117 | |||||||
| chr2:181003144 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19051C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003144 | |||||||
| chr2:181003207 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.245+19114A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003207 | |||||||
| chr2:181003272 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(21): Show |
28 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+19179G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003272 | |||||||
| chr2:181003359 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245+19266A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003359 | |||||||
| chr2:181003446 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0248 |
2 | NA18951.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.245+19353C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003446 | |||||||
| chr2:181003464 | CA | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19372delA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003464 | |||||||
| chr2:181003507 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+19414A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003507 | |||||||
| chr2:181003507 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.245+19414A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003507 | |||||||
| chr2:181003623 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19530T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003623 | |||||||
| chr2:181003633 | TA | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+19544delA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181003633 | ||||||
| chr2:181003649 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245+19556A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003649 | |||||||
| chr2:181003662 | T | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+19569T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003662 | |||||||
| chr2:181003706 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19613C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003706 | |||||||
| chr2:181003724 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19631T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003724 | |||||||
| chr2:181003789 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+19696T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003789 | |||||||
| chr2:181003809 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.245+19716C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003809 | |||||||
| chr2:181003872 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0151 |
2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.245+19779T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003872 | |||||||
| chr2:181003960 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19867G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003960 | |||||||
| chr2:181003981 | A | G | 5 | a0001c0001t0005g0123 a0001c0001t0005g0124 a0001c0001t0005g0125 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.245+19888A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003981 | |||||||
| chr2:181003990 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+19897T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181003990 | |||||||
| chr2:181004034 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.245+19941T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004034 | |||||||
| chr2:181004118 | AT | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+20028delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181004118 | ||||||
| chr2:181004192 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+20099A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004192 | |||||||
| chr2:181004384 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.245+20291C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004384 | |||||||
| chr2:181004447 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+20354G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004447 | |||||||
| chr2:181004461 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+20368C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004461 | |||||||
| chr2:181004526 | G | A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG00408.hp1 HG02135.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+20433G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004526 | |||||||
| chr2:181004537 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.245+20444G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004537 | |||||||
| chr2:181004605 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+20512T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004605 | |||||||
| chr2:181004628 | C | T | 1 | a0001c0001t0005g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.245+20535C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004628 | |||||||
| chr2:181004791 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+20698A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004791 | |||||||
| chr2:181004816 | G | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(74): Show |
83 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.245+20723G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004816 | |||||||
| chr2:181004834 | T | G | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.245+20741T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004834 | |||||||
| chr2:181004900 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.245+20807A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004900 | |||||||
| chr2:181004987 | T | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(124): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.245+20894T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181004987 | |||||||
| chr2:181005056 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0324 |
3 | HG01891.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.245+20963T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005056 | |||||||
| chr2:181005100 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+21007A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005100 | |||||||
| chr2:181005178 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+21085A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005178 | |||||||
| chr2:181005276 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.245+21183G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005276 | |||||||
| chr2:181005296 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.245+21203C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005296 | |||||||
| chr2:181005310 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0195 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.245+21217G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005310 | |||||||
| chr2:181005540 | C | CT | 6 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.245+21452dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181005540 | ||||||
| chr2:181005622 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.245+21529T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005622 | |||||||
| chr2:181005625 | C | CTG | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(37): Show |
intron_variant | MODIFIER | c.245+21537_245+2153 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181005625 | ||||||
| chr2:181005679 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.245+21586G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005679 | |||||||
| chr2:181005728 | A | G | 2 | a0001c0001t0005g0126 a0001c0001t0011g0121 |
2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.245+21635A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005728 | |||||||
| chr2:181005741 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+21648A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005741 | |||||||
| chr2:181005784 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+21691G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005784 | |||||||
| chr2:181005933 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.245+21840T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005933 | |||||||
| chr2:181005977 | T | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.245+21884T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005977 | |||||||
| chr2:181005978 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.245+21885T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181005978 | |||||||
| chr2:181006130 | C | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+22037C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006130 | |||||||
| chr2:181006219 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.245+22126A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006219 | |||||||
| chr2:181006346 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245+22253A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006346 | |||||||
| chr2:181006384 | AT | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.245+22296delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181006384 | ||||||
| chr2:181006557 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+22464A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006557 | |||||||
| chr2:181006612 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+22519T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006612 | |||||||
| chr2:181006683 | G | GAATT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+22590_245+2259 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006683 | |||||||
| chr2:181006700 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+22607A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006700 | |||||||
| chr2:181006735 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+22642G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006735 | |||||||
| chr2:181006736 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.245+22643G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006736 | |||||||
| chr2:181006739 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+22646C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006739 | |||||||
| chr2:181006851 | A | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+22758A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006851 | |||||||
| chr2:181006866 | A | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+22773A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006866 | |||||||
| chr2:181006932 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.245+22839A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006932 | |||||||
| chr2:181006985 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.245+22892A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181006985 | |||||||
| chr2:181007031 | A | T | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+22938A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007031 | |||||||
| chr2:181007061 | T | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+22968T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007061 | |||||||
| chr2:181007088 | C | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(121): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.245+22995C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007088 | |||||||
| chr2:181007174 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.245+23081A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007174 | |||||||
| chr2:181007191 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.245+23098C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007191 | |||||||
| chr2:181007199 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+23106C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007199 | |||||||
| chr2:181007241 | C | T | 7 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0049 others(4): Show |
7 | NA18951.hp1 NA18954.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.245+23148C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007241 | |||||||
| chr2:181007328 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+23235G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007328 | |||||||
| chr2:181007355 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+23262G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007355 | |||||||
| chr2:181007378 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+23285G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007378 | |||||||
| chr2:181007449 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.245+23356C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007449 | |||||||
| chr2:181007462 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+23369A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007462 | |||||||
| chr2:181007500 | GT | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
85 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.245+23421delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181007500 | ||||||
| chr2:181007500 | GTTTT | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+23418_245+2342 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181007500 | ||||||
| chr2:181007649 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.245+23556G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007649 | |||||||
| chr2:181007653 | T | C | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+23560T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007653 | |||||||
| chr2:181007696 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+23603A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007696 | |||||||
| chr2:181007760 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.245+23667A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007760 | |||||||
| chr2:181007767 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0003g0008 |
2 | HG01243.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.245+23674A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007767 | |||||||
| chr2:181007778 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.245+23685A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007778 | |||||||
| chr2:181007903 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+23810A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007903 | |||||||
| chr2:181007930 | T | C | 9 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+23837T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007930 | |||||||
| chr2:181007957 | T | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245+23864T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007957 | |||||||
| chr2:181007995 | G | A | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+23902G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181007995 | |||||||
| chr2:181008221 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+24128A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181008221 | |||||||
| chr2:181008325 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.245+24232A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181008325 | |||||||
| chr2:181008356 | G | T | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.245+24263G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181008356 | |||||||
| chr2:181008906 | CT | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(125): Show |
132 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.245+24829delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181008906 | ||||||
| chr2:181008906 | CTT | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.245+24828_245+2482 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181008906 | ||||||
| chr2:181008906 | CTTT | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0290 others(5): Show |
10 | HG01070.hp2 HG01361.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.245+24827_245+2482 others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181008906 | ||||||
| chr2:181008922 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.245+24829T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181008922 | |||||||
| chr2:181008934 | G | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.245+24841G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181008934 | |||||||
| chr2:181009024 | AG | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+24933delG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181009024 | ||||||
| chr2:181009322 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.245+25229A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181009322 | |||||||
| chr2:181009355 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+25262C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181009355 | |||||||
| chr2:181009429 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+25336G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181009429 | |||||||
| chr2:181009458 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+25365G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181009458 | |||||||
| chr2:181009513 | ATATTTAT others(9): Show |
A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.245+25441_245+2545 others(20): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181009513 | ||||||
| chr2:181009547 | ATTATT | A | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0281 others(9): Show |
12 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.245+25465_245+2546 others(9): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181009547 | ||||||
| chr2:181009562 | T | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+25469T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181009562 | |||||||
| chr2:181009613 | TCAGTATA others(2): Show |
T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+25522_245+2553 others(13): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181009613 | ||||||
| chr2:181009923 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+25830A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181009923 | |||||||
| chr2:181010221 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02630.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.245+26128A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010221 | |||||||
| chr2:181010247 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.245+26154A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010247 | |||||||
| chr2:181010298 | A | G | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG01074.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.245+26205A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010298 | |||||||
| chr2:181010320 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.245+26227A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010320 | |||||||
| chr2:181010514 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.245+26421T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010514 | |||||||
| chr2:181010551 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245+26458T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010551 | |||||||
| chr2:181010557 | C | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(25): Show |
32 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.245+26464C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010557 | |||||||
| chr2:181010648 | A | T | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.245+26555A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010648 | |||||||
| chr2:181010667 | A | G | 9 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+26574A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010667 | |||||||
| chr2:181010807 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.245+26714T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010807 | |||||||
| chr2:181010874 | C | CTTTTA | 40 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
41 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(38): Show |
intron_variant | MODIFIER | c.245+26783_245+2678 others(9): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181010874 | ||||||
| chr2:181010984 | G | A | 4 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0305 others(1): Show |
4 | HG00423.hp2 HG03927.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+26891G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181010984 | |||||||
| chr2:181011018 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.245+26925T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011018 | |||||||
| chr2:181011063 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0301 a0001c0001t0001g0302 |
4 | HG01884.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+26970G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011063 | |||||||
| chr2:181011071 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245+26978C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011071 | |||||||
| chr2:181011145 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+27052G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011145 | |||||||
| chr2:181011573 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245+27480A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011573 | |||||||
| chr2:181011693 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.245+27600G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011693 | |||||||
| chr2:181011994 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+27901A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181011994 | |||||||
| chr2:181012085 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245+27992A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181012085 | |||||||
| chr2:181012207 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+28114A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181012207 | |||||||
| chr2:181012332 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+28239T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181012332 | |||||||
| chr2:181013097 | G | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+29004G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013097 | |||||||
| chr2:181013152 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(37): Show |
intron_variant | MODIFIER | c.245+29059A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013152 | |||||||
| chr2:181013161 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(18): Show |
24 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.245+29068G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013161 | |||||||
| chr2:181013383 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.245+29290G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013383 | |||||||
| chr2:181013412 | A | G | 6 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.245+29319A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013412 | |||||||
| chr2:181013433 | C | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(37): Show |
intron_variant | MODIFIER | c.245+29340C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013433 | |||||||
| chr2:181013477 | CTGTTGGC others(22): Show |
C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+29392_245+2942 others(33): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181013477 | ||||||
| chr2:181013509 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.245+29416T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013509 | |||||||
| chr2:181013726 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.245+29633C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013726 | |||||||
| chr2:181013820 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.245+29727G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013820 | |||||||
| chr2:181013884 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.245+29791A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013884 | |||||||
| chr2:181013924 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.245+29831A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013924 | |||||||
| chr2:181013996 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(21): Show |
28 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+29903G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181013996 | |||||||
| chr2:181014043 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.245+29950C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181014043 | |||||||
| chr2:181014132 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+30039G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181014132 | |||||||
| chr2:181014155 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.245+30062G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181014155 | |||||||
| chr2:181014782 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.245+30689G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181014782 | |||||||
| chr2:181015074 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245+30981G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015074 | |||||||
| chr2:181015285 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+31192A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015285 | |||||||
| chr2:181015314 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00099.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.245+31221A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015314 | |||||||
| chr2:181015783 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18962.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.245+31690T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015783 | |||||||
| chr2:181015813 | G | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+31720G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015813 | |||||||
| chr2:181015835 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+31742C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015835 | |||||||
| chr2:181015856 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.245+31763G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015856 | |||||||
| chr2:181015990 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.245+31897T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181015990 | |||||||
| chr2:181016003 | T | TAAAATTT others(303): Show |
7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+31926_245+3192 others(314): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181016003 | ||||||
| chr2:181016003 | T | TAAAATTT others(303): Show |
48 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.245+31926_245+3192 others(314): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181016003 | ||||||
| chr2:181016003 | T | TAAAATTT others(304): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0056 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.245+31926_245+3192 others(315): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181016003 | ||||||
| chr2:181016014 | C | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(124): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.245+31921C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016014 | |||||||
| chr2:181016113 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+32020A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016113 | |||||||
| chr2:181016117 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.245+32024A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016117 | |||||||
| chr2:181016120 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0193 a0001c0001t0001g0194 |
4 | HG02451.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+32027A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016120 | |||||||
| chr2:181016121 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.245+32028A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016121 | |||||||
| chr2:181016134 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0322 |
3 | HG01081.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.245+32041G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016134 | |||||||
| chr2:181016223 | C | T | 38 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
39 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.245+32130C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016223 | |||||||
| chr2:181016250 | T | A | 47 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0024 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.245+32157T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016250 | |||||||
| chr2:181016318 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+32225G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016318 | |||||||
| chr2:181016329 | C | A | 1 | a0001c0001t0002g0028 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.245+32236C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016329 | |||||||
| chr2:181016692 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.245+32599G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016692 | |||||||
| chr2:181016745 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.245+32652G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016745 | |||||||
| chr2:181016863 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+32770T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016863 | |||||||
| chr2:181016957 | C | T | 1 | a0001c0001t0005g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245+32864C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181016957 | |||||||
| chr2:181017198 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18977.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.245+33105G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017198 | |||||||
| chr2:181017198 | G | GGGAGTAT others(46): Show |
1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.245+33108_245+3316 others(57): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181017198 | ||||||
| chr2:181017200 | G | GA | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+33108dupA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181017200 | ||||||
| chr2:181017312 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02630.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.245+33219G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017312 | |||||||
| chr2:181017481 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.245+33388C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017481 | |||||||
| chr2:181017586 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245+33493G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017586 | |||||||
| chr2:181017611 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+33518A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017611 | |||||||
| chr2:181017651 | A | AT | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.245+33569dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181017651 | ||||||
| chr2:181017651 | A | ATT | 41 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
42 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(39): Show |
intron_variant | MODIFIER | c.245+33568_245+3356 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181017651 | ||||||
| chr2:181017796 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.245+33703C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017796 | |||||||
| chr2:181017822 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+33729A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017822 | |||||||
| chr2:181017867 | G | GAGGGCCC others(17): Show |
1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.245+33775_245+3379 others(28): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181017867 | ||||||
| chr2:181017919 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245+33826C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181017919 | |||||||
| chr2:181018015 | A | G | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(122): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.245+33922A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018015 | |||||||
| chr2:181018152 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.245+34059G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018152 | |||||||
| chr2:181018158 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+34065T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018158 | |||||||
| chr2:181018184 | TA | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+34096delA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018184 | ||||||
| chr2:181018320 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(20): Show |
27 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.245+34227T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018320 | |||||||
| chr2:181018331 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.245+34238G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018331 | |||||||
| chr2:181018331 | G | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+34238G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018331 | |||||||
| chr2:181018370 | G | GTA | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0107 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.245+34293_245+3429 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018370 | ||||||
| chr2:181018370 | GTA | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+34293_245+3429 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018370 | ||||||
| chr2:181018372 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0229 |
2 | HG01891.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.245+34279A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018372 | |||||||
| chr2:181018412 | A | T | 1 | a0001c0001t0002g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.245+34319A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018412 | |||||||
| chr2:181018598 | G | GT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0069 others(54): Show |
59 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.245+34523dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018598 | ||||||
| chr2:181018598 | G | GTT | 32 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0150 others(29): Show |
33 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.245+34522_245+3452 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018598 | ||||||
| chr2:181018598 | GT | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0097 others(3): Show |
7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.245+34523delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018598 | ||||||
| chr2:181018598 | GTTTTT | G | 53 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(50): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.245+34519_245+3452 others(9): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181018598 | ||||||
| chr2:181018715 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.245+34622A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018715 | |||||||
| chr2:181018844 | T | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+34751T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181018844 | |||||||
| chr2:181019066 | C | T | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(122): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.245+34973C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181019066 | |||||||
| chr2:181019160 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(21): Show |
28 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+35067G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181019160 | |||||||
| chr2:181019308 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+35215A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181019308 | |||||||
| chr2:181019696 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.245+35603A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181019696 | |||||||
| chr2:181019837 | C | CT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.245+35752dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181019837 | ||||||
| chr2:181019880 | A | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245+35787A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181019880 | |||||||
| chr2:181020117 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+36024A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020117 | |||||||
| chr2:181020209 | G | GCCGT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.245+36117_245+3612 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181020209 | ||||||
| chr2:181020217 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245+36124C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020217 | |||||||
| chr2:181020218 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.245+36125C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020218 | |||||||
| chr2:181020333 | T | C | 7 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.245+36240T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020333 | |||||||
| chr2:181020486 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.245+36393G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020486 | |||||||
| chr2:181020503 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.245+36410G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020503 | |||||||
| chr2:181020568 | G | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.245+36475G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020568 | |||||||
| chr2:181020699 | C | T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0127 a0001c0001t0001g0184 others(7): Show |
10 | HG01175.hp1 HG02015.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.245+36606C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020699 | |||||||
| chr2:181020758 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.245+36665A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020758 | |||||||
| chr2:181020873 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.245+36780T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020873 | |||||||
| chr2:181020894 | A | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.246-36799A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020894 | |||||||
| chr2:181020911 | TTAGGGAA others(10): Show |
T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(60): Show |
68 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.246-36777_246-3676 others(21): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181020911 | ||||||
| chr2:181020912 | T | TAGGGAAT others(5): Show |
1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.246-36777_246-3676 others(16): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181020912 | ||||||
| chr2:181020960 | T | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36733T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181020960 | |||||||
| chr2:181021085 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.246-36608G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021085 | |||||||
| chr2:181021264 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36429A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021264 | |||||||
| chr2:181021265 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36428T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021265 | |||||||
| chr2:181021268 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36425A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021268 | |||||||
| chr2:181021269 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36424T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021269 | |||||||
| chr2:181021273 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36420A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021273 | |||||||
| chr2:181021280 | T | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36413T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021280 | |||||||
| chr2:181021292 | T | G | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36401T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021292 | |||||||
| chr2:181021297 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(59): Show |
67 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.246-36396G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021297 | |||||||
| chr2:181021357 | C | CT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(18): Show |
25 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.246-36326dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021357 | ||||||
| chr2:181021357 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36336C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021357 | |||||||
| chr2:181021357 | CT | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(47): Show |
51 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.246-36326delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021357 | ||||||
| chr2:181021358 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36335T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021358 | |||||||
| chr2:181021378 | CT | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.246-36308delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021378 | ||||||
| chr2:181021423 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36270T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021423 | |||||||
| chr2:181021429 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36264C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021429 | |||||||
| chr2:181021431 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36262T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021431 | |||||||
| chr2:181021433 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36260C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021433 | |||||||
| chr2:181021434 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36259T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021434 | |||||||
| chr2:181021437 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36256C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021437 | |||||||
| chr2:181021437 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.246-36256C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021437 | |||||||
| chr2:181021438 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36255T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021438 | |||||||
| chr2:181021439 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36254T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021439 | |||||||
| chr2:181021467 | T | TC | 4 | a0001c0001t0001g0072 a0001c0001t0001g0185 a0001c0001t0001g0203 others(1): Show |
4 | HG02602.hp2 NA18961.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-36226_246-3622 others(5): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021467 | |||||||
| chr2:181021467 | T | TTC | 3 | a0001c0001t0001g0189 a0001c0001t0001g0278 a0001c0001t0001g0319 |
3 | HG01074.hp1 NA18964.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.246-36222_246-3622 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021467 | ||||||
| chr2:181021468 | T | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0115 a0001c0001t0001g0202 others(1): Show |
4 | HG00438.hp1 HG00741.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-36225T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021468 | |||||||
| chr2:181021468 | T | TC | 54 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0066 others(51): Show |
55 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.246-36224dupC | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021468 | ||||||
| chr2:181021468 | T | TCC | 3 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0112 |
3 | HG00438.hp2 HG01106.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.246-36224_246-3622 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021468 | ||||||
| chr2:181021470 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.246-36223T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021470 | |||||||
| chr2:181021472 | T | C | 1 | a0002c0002t0003g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.246-36221T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021472 | |||||||
| chr2:181021475 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.246-36218C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021475 | |||||||
| chr2:181021476 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.246-36217T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021476 | |||||||
| chr2:181021483 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246-36210C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021483 | |||||||
| chr2:181021489 | CTTCCT | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0147 |
3 | HG03098.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.246-36187_246-3618 others(9): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021489 | ||||||
| chr2:181021508 | CTTCTTTC others(4): Show |
C | 1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36184_246-3617 others(15): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021508 | |||||||
| chr2:181021524 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36169T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021524 | |||||||
| chr2:181021528 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36165T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021528 | |||||||
| chr2:181021537 | T | TCTACCCT others(1389): Show |
1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36156_246-3615 others(1400): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021537 | |||||||
| chr2:181021541 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36152T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021541 | |||||||
| chr2:181021544 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36149T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021544 | |||||||
| chr2:181021545 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36148A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021545 | |||||||
| chr2:181021546 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36147A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021546 | |||||||
| chr2:181021547 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36146A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021547 | |||||||
| chr2:181021548 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36145T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021548 | |||||||
| chr2:181021549 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36144A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021549 | |||||||
| chr2:181021551 | A | ACTCC | 50 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(47): Show |
52 | HG00544.hp1 HG00558.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.246-36139_246-3613 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021551 | ||||||
| chr2:181021551 | A | ACTCCCTT others(1281): Show |
1 | a0001c0001t0001g0060 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1292): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021551 | ||||||
| chr2:181021551 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36142A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021551 | |||||||
| chr2:181021554 | C | CCCTCCCT others(197): Show |
6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-36136_246-3613 others(208): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021554 | ||||||
| chr2:181021554 | C | CCCTCCCT others(177): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(6): Show |
12 | HG01361.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.246-36136_246-3613 others(188): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021554 | ||||||
| chr2:181021554 | C | CCCTCCCT others(129): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0294 others(9): Show |
13 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.246-36136_246-3613 others(140): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021554 | ||||||
| chr2:181021554 | C | CCCTCCCT others(125): Show |
5 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | NA18959.hp2 NA18969.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-36136_246-3613 others(136): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021554 | ||||||
| chr2:181021554 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246-36139C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021554 | |||||||
| chr2:181021557 | T | TTCCTTCC others(679): Show |
1 | a0001c0001t0001g0179 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(690): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021557 | ||||||
| chr2:181021558 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.246-36135T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021558 | |||||||
| chr2:181021562 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(30): Show |
37 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.246-36131T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021562 | |||||||
| chr2:181021562 | T | TCCTTCCT others(1333): Show |
1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1344): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(669): Show |
1 | a0001c0001t0001g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(680): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(709): Show |
1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(720): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(641): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(652): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(625): Show |
1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(636): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(645): Show |
3 | a0001c0001t0001g0109 a0001c0001t0001g0301 a0001c0001t0008g0108 |
3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(656): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1324): Show |
1 | a0001c0001t0001g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1335): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1241): Show |
1 | a0001c0001t0001g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1252): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1377): Show |
1 | a0001c0001t0001g0117 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1388): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1277): Show |
1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1288): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1281): Show |
1 | a0001c0001t0001g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1292): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1329): Show |
1 | a0001c0001t0001g0077 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1340): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1325): Show |
1 | a0001c0001t0003g0078 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1336): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1325): Show |
4 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0083 others(1): Show |
4 | HG02145.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1336): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1289): Show |
1 | a0001c0001t0001g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1300): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1278): Show |
1 | a0001c0001t0003g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1289): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1277): Show |
3 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0104 |
3 | HG02559.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1288): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1277): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0097 |
2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1288): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1441): Show |
1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1452): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1401): Show |
1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1412): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1405): Show |
1 | a0001c0001t0001g0116 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1416): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1401): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG00642.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1412): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1400): Show |
1 | a0001c0001t0001g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1411): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1421): Show |
1 | a0001c0001t0003g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1432): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1321): Show |
1 | a0001c0001t0001g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1332): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1321): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0084 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1332): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1317): Show |
1 | a0001c0001t0001g0070 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1328): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1321): Show |
1 | a0001c0001t0001g0071 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1332): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1315): Show |
1 | a0001c0001t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1326): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1351): Show |
1 | a0001c0001t0010g0012 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1362): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1333): Show |
1 | a0001c0001t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1344): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1241): Show |
1 | a0001c0001t0001g0091 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1252): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1313): Show |
1 | a0001c0001t0001g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1324): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1353): Show |
1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1364): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1349): Show |
2 | a0001c0001t0001g0080 a0001c0001t0008g0062 |
2 | NA18977.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1360): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1549): Show |
1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1560): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1349): Show |
3 | a0001c0001t0001g0074 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG01243.hp1 HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1360): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1337): Show |
1 | a0001c0001t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1348): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1349): Show |
2 | a0001c0001t0001g0063 a0002c0002t0003g0067 |
2 | HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(1360): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1345): Show |
1 | a0001c0001t0001g0066 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1356): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1293): Show |
1 | a0001c0001t0001g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1304): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1349): Show |
1 | a0001c0001t0001g0072 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1360): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1370): Show |
1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1381): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1254): Show |
1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1265): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(693): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0193 a0001c0001t0001g0194 |
4 | HG02451.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-36120_246-3611 others(704): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(493): Show |
1 | a0001c0001t0001g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(504): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0003g0243 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
2 | a0001c0001t0001g0209 a0001c0001t0001g0238 |
2 | HG02080.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(675): Show |
1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(686): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(669): Show |
1 | a0001c0001t0001g0277 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(680): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(670): Show |
1 | a0001c0001t0001g0278 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(681): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(669): Show |
2 | a0001c0001t0001g0276 a0001c0001t0001g0279 |
2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(680): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(674): Show |
1 | a0001c0001t0003g0251 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(685): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(645): Show |
1 | a0001c0001t0001g0210 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(656): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0003g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0227 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0192 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(679): Show |
1 | a0001c0001t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(690): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0178 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0228 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
10 | a0001c0001t0001g0004 a0001c0001t0001g0181 a0001c0001t0001g0183 others(7): Show |
11 | HG00544.hp2 HG01258.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1433): Show |
1 | a0001c0001t0003g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1444): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(669): Show |
1 | a0001c0001t0001g0131 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(680): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0258 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(661): Show |
1 | a0001c0001t0001g0259 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(672): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(753): Show |
1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(764): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0321 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(725): Show |
3 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0003g0213 |
3 | NA18942.hp2 NA18950.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(736): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(805): Show |
1 | a0001c0001t0001g0267 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(816): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0132 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0242 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(685): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG00733.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(696): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(701): Show |
1 | a0001c0001t0001g0218 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(712): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0003g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
22 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0148 others(19): Show |
22 | HG00408.hp2 HG00609.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(725): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0324 |
3 | HG01891.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(736): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(237): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0248 |
2 | NA18951.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(248): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0275 |
2 | HG00438.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(1137): Show |
1 | a0001c0001t0001g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(1148): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0206 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0225 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(677): Show |
1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(688): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18954.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
1 | a0001c0001t0001g0207 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(673): Show |
5 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0001t0001g0309 others(2): Show |
5 | HG01074.hp1 HG01515.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.246-36120_246-3611 others(684): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(665): Show |
1 | a0001c0001t0003g0196 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(676): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0233 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(585): Show |
1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(596): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(680): Show |
1 | a0001c0001t0001g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(691): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(769): Show |
1 | a0001c0001t0001g0261 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(780): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(729): Show |
1 | a0001c0001t0003g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(740): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0262 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(649): Show |
1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(660): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0003g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
1 | a0001c0001t0001g0263 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(669): Show |
1 | a0001c0001t0001g0185 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(680): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(665): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.246-36120_246-3611 others(676): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(681): Show |
4 | a0001c0001t0001g0189 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG00140.hp1 HG02738.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-36120_246-3611 others(692): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(649): Show |
1 | a0001c0001t0001g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(660): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(657): Show |
1 | a0001c0001t0001g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.246-36120_246-3611 others(668): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(665): Show |
1 | a0001c0001t0003g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(676): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(679): Show |
1 | a0001c0001t0001g0320 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(690): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021562 | T | TCCTTCCT others(753): Show |
1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.246-36120_246-3611 others(764): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021562 | ||||||
| chr2:181021574 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.246-36119C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021574 | |||||||
| chr2:181021578 | C | CCCTCCCT others(69): Show |
13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-36092_246-3609 others(80): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021578 | ||||||
| chr2:181021578 | C | CCCTCCCT others(89): Show |
37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-36100_246-3609 others(100): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021578 | ||||||
| chr2:181021578 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.246-36115C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021578 | |||||||
| chr2:181021582 | C | T | 7 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.246-36111C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021582 | |||||||
| chr2:181021586 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.246-36107T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021586 | |||||||
| chr2:181021590 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.246-36103T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021590 | |||||||
| chr2:181021602 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-36091T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021602 | |||||||
| chr2:181021619 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0246 |
2 | HG01109.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.246-36074T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021619 | |||||||
| chr2:181021622 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-36071C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021622 | |||||||
| chr2:181021626 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0246 |
2 | HG01109.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.246-36067C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021626 | |||||||
| chr2:181021630 | T | TCCTCCCT others(663): Show |
1 | a0001c0001t0001g0246 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.246-36063_246-3606 others(674): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021630 | |||||||
| chr2:181021631 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-36062T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021631 | |||||||
| chr2:181021632 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-36061T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021632 | |||||||
| chr2:181021632 | T | TTTCC | 42 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0063 others(39): Show |
42 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.246-36029_246-3602 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(1): Show |
29 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(26): Show |
29 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.246-36033_246-3602 others(12): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(5): Show |
64 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0107 others(61): Show |
66 | HG00408.hp2 HG01071.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.246-36037_246-3602 others(16): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(9): Show |
42 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(39): Show |
43 | HG00140.hp1 HG00558.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.246-36041_246-3602 others(20): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(13): Show |
66 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(63): Show |
68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.246-36045_246-3602 others(24): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(17): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0150 others(19): Show |
23 | HG00140.hp2 HG00280.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.246-36049_246-3602 others(28): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(21): Show |
11 | a0001c0001t0001g0226 a0001c0001t0001g0322 a0001c0001t0002g0031 others(8): Show |
11 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.246-36053_246-3602 others(32): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | T | TTTCCTTC others(25): Show |
1 | a0001c0001t0002g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.246-36057_246-3602 others(36): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021632 | TTTCCTTC others(1): Show |
T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
30 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.246-36033_246-3602 others(12): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021632 | ||||||
| chr2:181021642 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-36051T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021642 | |||||||
| chr2:181021644 | C | CTCCCTCC others(1309): Show |
1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-36048_246-3604 others(1320): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021644 | ||||||
| chr2:181021652 | CTTCCTTC others(9): Show |
C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-36028_246-3601 others(20): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181021652 | ||||||
| chr2:181021849 | T | C | 1 | a0001c0001t0002g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246-35844T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021849 | |||||||
| chr2:181021938 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246-35755A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181021938 | |||||||
| chr2:181022063 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.246-35630G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022063 | |||||||
| chr2:181022311 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-35382A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022311 | |||||||
| chr2:181022459 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-35234A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022459 | |||||||
| chr2:181022496 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.246-35197A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022496 | |||||||
| chr2:181022652 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.246-35041G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022652 | |||||||
| chr2:181022722 | C | CA | 27 | a0001c0001t0001g0059 a0001c0001t0001g0089 a0001c0001t0001g0093 others(24): Show |
27 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.246-34962dupA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181022722 | ||||||
| chr2:181022731 | A | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-34962A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022731 | |||||||
| chr2:181022739 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.246-34954C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022739 | |||||||
| chr2:181022739 | C | CA | 9 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0132 others(6): Show |
9 | HG00558.hp1 HG01515.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-34944dupA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181022739 | ||||||
| chr2:181022740 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.246-34953A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022740 | |||||||
| chr2:181022760 | T | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.246-34933T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181022760 | |||||||
| chr2:181022902 | T | TG | 5 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.246-34790dupG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181022902 | ||||||
| chr2:181023131 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-34562C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023131 | |||||||
| chr2:181023514 | G | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-34179G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023514 | |||||||
| chr2:181023595 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-34098A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023595 | |||||||
| chr2:181023790 | ATCTACC | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-33901_246-3389 others(10): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181023790 | ||||||
| chr2:181023791 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.246-33902T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023791 | |||||||
| chr2:181023828 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-33865G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023828 | |||||||
| chr2:181023837 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-33856A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023837 | |||||||
| chr2:181023870 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-33823C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023870 | |||||||
| chr2:181023915 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18977.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.246-33778A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023915 | |||||||
| chr2:181023990 | T | C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0156 a0001c0001t0001g0161 others(2): Show |
5 | HG02056.hp2 NA18971.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.246-33703T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181023990 | |||||||
| chr2:181024071 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-33622G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024071 | |||||||
| chr2:181024116 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.246-33577A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024116 | |||||||
| chr2:181024179 | A | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | NA18989.hp2 NA18993.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-33514A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024179 | |||||||
| chr2:181024265 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.246-33428G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024265 | |||||||
| chr2:181024267 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.246-33426G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024267 | |||||||
| chr2:181024335 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.246-33358G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024335 | |||||||
| chr2:181024361 | C | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0053 |
2 | NA18987.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.246-33332C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024361 | |||||||
| chr2:181024460 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0301 a0001c0001t0001g0302 |
4 | HG01884.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-33233C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024460 | |||||||
| chr2:181024462 | A | G | 6 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.246-33231A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024462 | |||||||
| chr2:181024566 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-33127T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024566 | |||||||
| chr2:181024571 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0273 |
3 | HG02071.hp2 HG02080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.246-33122T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024571 | |||||||
| chr2:181024675 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.246-33018C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024675 | |||||||
| chr2:181024773 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-32920A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024773 | |||||||
| chr2:181024896 | A | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(22): Show |
29 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.246-32797A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181024896 | |||||||
| chr2:181025122 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.246-32571A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025122 | |||||||
| chr2:181025397 | T | TC | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-32296_246-3229 others(5): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025397 | |||||||
| chr2:181025400 | TCTA | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-32292_246-3229 others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025400 | |||||||
| chr2:181025403 | A | AT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
223 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.246-32284dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181025403 | ||||||
| chr2:181025478 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-32215C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025478 | |||||||
| chr2:181025501 | T | TTGCC | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-32190_246-3218 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181025501 | ||||||
| chr2:181025539 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-32154C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025539 | |||||||
| chr2:181025630 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.246-32063C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025630 | |||||||
| chr2:181025667 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246-32026T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025667 | |||||||
| chr2:181025689 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.246-32004A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025689 | |||||||
| chr2:181025813 | C | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0150 others(19): Show |
22 | HG01981.hp2 HG02056.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.246-31880C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025813 | |||||||
| chr2:181025871 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0188 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.246-31822C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025871 | |||||||
| chr2:181025924 | A | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-31769A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181025924 | |||||||
| chr2:181026092 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.246-31601C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026092 | |||||||
| chr2:181026160 | C | A | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-31533C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026160 | |||||||
| chr2:181026262 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.246-31431T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026262 | |||||||
| chr2:181026317 | AT | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-31366delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181026317 | ||||||
| chr2:181026399 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-31294C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026399 | |||||||
| chr2:181026409 | C | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-31284C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026409 | |||||||
| chr2:181026415 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-31278T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026415 | |||||||
| chr2:181026459 | A | G | 7 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0049 others(4): Show |
7 | NA18951.hp1 NA18954.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.246-31234A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026459 | |||||||
| chr2:181026514 | A | AT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(27): Show |
34 | HG00423.hp2 HG00738.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.246-31164dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181026514 | ||||||
| chr2:181026514 | AT | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0072 a0001c0001t0001g0074 others(15): Show |
19 | HG01168.hp2 HG01169.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.246-31164delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181026514 | ||||||
| chr2:181026593 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-31100T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026593 | |||||||
| chr2:181026661 | C | T | 9 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-31032C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026661 | |||||||
| chr2:181026681 | T | G | 1 | a0001c0001t0002g0033 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.246-31012T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026681 | |||||||
| chr2:181026695 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.246-30998A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026695 | |||||||
| chr2:181026740 | CT | C | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-30949delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181026740 | ||||||
| chr2:181026873 | TATA | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-30816_246-3081 others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181026873 | ||||||
| chr2:181026953 | T | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.246-30740T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026953 | |||||||
| chr2:181026995 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.246-30698T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181026995 | |||||||
| chr2:181027096 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.246-30597T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181027096 | |||||||
| chr2:181027206 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.246-30487C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181027206 | |||||||
| chr2:181027207 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246-30486G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181027207 | |||||||
| chr2:181027260 | G | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0175 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.246-30433G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181027260 | |||||||
| chr2:181027709 | C | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-29984C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181027709 | |||||||
| chr2:181027931 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246-29762C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181027931 | |||||||
| chr2:181028125 | T | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0172 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.246-29568T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028125 | |||||||
| chr2:181028128 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0172 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.246-29565T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028128 | |||||||
| chr2:181028161 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.246-29532C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028161 | |||||||
| chr2:181028178 | A | G | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0286 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-29515A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028178 | |||||||
| chr2:181028186 | A | T | 1 | a0001c0001t0001g0273 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.246-29507A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028186 | |||||||
| chr2:181028221 | T | A | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-29472T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028221 | |||||||
| chr2:181028323 | C | T | 1 | a0001c0001t0002g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.246-29370C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028323 | |||||||
| chr2:181028345 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-29348C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028345 | |||||||
| chr2:181028397 | G | A | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-29296G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028397 | |||||||
| chr2:181028540 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.246-29153C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028540 | |||||||
| chr2:181028608 | T | C | 1 | a0001c0001t0003g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.246-29085T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028608 | |||||||
| chr2:181028638 | TC | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0106 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.246-29053delC | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181028638 | ||||||
| chr2:181028647 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-29046T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028647 | |||||||
| chr2:181028928 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-28765T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181028928 | |||||||
| chr2:181029097 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-28596G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029097 | |||||||
| chr2:181029160 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-28533A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029160 | |||||||
| chr2:181029220 | A | G | 1 | a0001c0001t0002g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.246-28473A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029220 | |||||||
| chr2:181029486 | T | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.246-28207T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029486 | |||||||
| chr2:181029567 | TG | T | 8 | a0001c0001t0004g0042 a0001c0001t0004g0045 a0001c0001t0004g0046 others(5): Show |
8 | NA18951.hp1 NA18954.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-28125delG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029567 | |||||||
| chr2:181029568 | G | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.246-28125G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029568 | |||||||
| chr2:181029659 | CT | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.246-28014delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029659 | ||||||
| chr2:181029659 | CTT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(38): Show |
45 | HG00423.hp2 HG00738.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.246-28015_246-2801 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029659 | ||||||
| chr2:181029659 | CTTT | C | 11 | a0001c0001t0001g0265 a0001c0001t0001g0300 a0001c0001t0001g0303 others(8): Show |
11 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.246-28016_246-2801 others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029659 | ||||||
| chr2:181029659 | CTTTT | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.246-28017_246-2801 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029659 | ||||||
| chr2:181029782 | A | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-27911A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029782 | |||||||
| chr2:181029782 | ATATTGAT others(1): Show |
A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-27909_246-2790 others(12): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029782 | ||||||
| chr2:181029791 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-27902T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029791 | |||||||
| chr2:181029837 | C | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-27856C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029837 | |||||||
| chr2:181029839 | C | CT | 31 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
34 | HG00423.hp2 HG01081.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.246-27838dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029839 | ||||||
| chr2:181029839 | C | CTT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0293 others(7): Show |
11 | HG00738.hp1 HG01243.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-27839_246-2783 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029839 | ||||||
| chr2:181029839 | CT | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-27838delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181029839 | ||||||
| chr2:181029840 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-27853T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029840 | |||||||
| chr2:181029860 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.246-27833C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029860 | |||||||
| chr2:181029866 | C | G | 1 | a0001c0001t0002g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.246-27827C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029866 | |||||||
| chr2:181029962 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-27731G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029962 | |||||||
| chr2:181029989 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-27704A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181029989 | |||||||
| chr2:181030041 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.246-27652C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030041 | |||||||
| chr2:181030047 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.246-27646T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030047 | |||||||
| chr2:181030053 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.246-27640T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030053 | |||||||
| chr2:181030084 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246-27609G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030084 | |||||||
| chr2:181030148 | A | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02630.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.246-27545A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030148 | |||||||
| chr2:181030171 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-27522G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030171 | |||||||
| chr2:181030250 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.246-27443A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030250 | |||||||
| chr2:181030295 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.246-27398T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030295 | |||||||
| chr2:181030309 | A | G | 18 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0173 others(15): Show |
18 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.246-27384A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030309 | |||||||
| chr2:181030363 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.246-27330G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030363 | |||||||
| chr2:181030414 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-27279G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030414 | |||||||
| chr2:181030423 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-27270T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030423 | |||||||
| chr2:181030433 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0301 a0001c0001t0001g0302 |
4 | HG01884.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-27260A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030433 | |||||||
| chr2:181030459 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.246-27234C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030459 | |||||||
| chr2:181030586 | A | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(22): Show |
29 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.246-27107A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030586 | |||||||
| chr2:181030676 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.246-27017C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030676 | |||||||
| chr2:181030740 | TC | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-26950delC | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181030740 | ||||||
| chr2:181030744 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
224 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.246-26949A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030744 | |||||||
| chr2:181030752 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-26941A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030752 | |||||||
| chr2:181030813 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0006g0022 |
2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.246-26880A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030813 | |||||||
| chr2:181030836 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0188 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.246-26857T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030836 | |||||||
| chr2:181030973 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.246-26720C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030973 | |||||||
| chr2:181030974 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-26719G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030974 | |||||||
| chr2:181030994 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.246-26699A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181030994 | |||||||
| chr2:181031126 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-26567A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181031126 | |||||||
| chr2:181031490 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-26203G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181031490 | |||||||
| chr2:181031511 | TTTTA | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
9 | HG01168.hp1 HG01169.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-26173_246-2617 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181031511 | ||||||
| chr2:181031537 | T | C | 8 | a0001c0001t0004g0042 a0001c0001t0004g0045 a0001c0001t0004g0046 others(5): Show |
8 | NA18951.hp1 NA18954.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-26156T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181031537 | |||||||
| chr2:181031727 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.246-25966C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181031727 | |||||||
| chr2:181031743 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0266 |
2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.246-25950A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181031743 | |||||||
| chr2:181031920 | G | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-25773G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181031920 | |||||||
| chr2:181032197 | A | G | 6 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.246-25496A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032197 | |||||||
| chr2:181032243 | G | A | 9 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-25450G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032243 | |||||||
| chr2:181032394 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.246-25299G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032394 | |||||||
| chr2:181032486 | A | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0293 others(12): Show |
16 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.246-25207A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032486 | |||||||
| chr2:181032627 | T | A | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0286 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-25066T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032627 | |||||||
| chr2:181032676 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(35): Show |
43 | HG00423.hp2 HG00738.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.246-25017A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032676 | |||||||
| chr2:181032692 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-25001C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181032692 | |||||||
| chr2:181033142 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-24551G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033142 | |||||||
| chr2:181033229 | C | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0106 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.246-24464C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033229 | |||||||
| chr2:181033328 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(22): Show |
28 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.246-24365G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033328 | |||||||
| chr2:181033344 | G | A | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-24349G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033344 | |||||||
| chr2:181033357 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.246-24336G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033357 | |||||||
| chr2:181033358 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.246-24335C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033358 | |||||||
| chr2:181033360 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-24333T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033360 | |||||||
| chr2:181033388 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-24305T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033388 | |||||||
| chr2:181033539 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246-24154T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033539 | |||||||
| chr2:181033615 | C | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-24078C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033615 | |||||||
| chr2:181033902 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-23791T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181033902 | |||||||
| chr2:181034003 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.246-23690C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034003 | |||||||
| chr2:181034004 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.246-23689A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034004 | |||||||
| chr2:181034286 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246-23407A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034286 | |||||||
| chr2:181034287 | T | C | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.246-23406T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034287 | |||||||
| chr2:181034533 | G | C | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.246-23160G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034533 | |||||||
| chr2:181034597 | A | G | 48 | a0001c0001t0001g0103 a0001c0001t0002g0015 a0001c0001t0002g0023 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.246-23096A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034597 | |||||||
| chr2:181034598 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.246-23095G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034598 | |||||||
| chr2:181034632 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.246-23061G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034632 | |||||||
| chr2:181034653 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-23040G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034653 | |||||||
| chr2:181034659 | T | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-23034T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034659 | |||||||
| chr2:181034684 | A | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0254 |
2 | NA18969.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.246-23009A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034684 | |||||||
| chr2:181034687 | A | AAAAAG | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-23002_246-2299 others(9): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181034687 | ||||||
| chr2:181034708 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0290 others(3): Show |
8 | HG01361.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-22985A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034708 | |||||||
| chr2:181034709 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.246-22984G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034709 | |||||||
| chr2:181034788 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-22905G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034788 | |||||||
| chr2:181034852 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.246-22841T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034852 | |||||||
| chr2:181034863 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-22830T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034863 | |||||||
| chr2:181034870 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.246-22823T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034870 | |||||||
| chr2:181034900 | A | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0293 others(14): Show |
18 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.246-22793A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034900 | |||||||
| chr2:181034989 | A | G | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.246-22704A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181034989 | |||||||
| chr2:181035017 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.246-22676A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035017 | |||||||
| chr2:181035028 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.246-22665C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035028 | |||||||
| chr2:181035077 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-22616C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035077 | |||||||
| chr2:181035109 | A | C | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.246-22584A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035109 | |||||||
| chr2:181035234 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.246-22459A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035234 | |||||||
| chr2:181035416 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-22277A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035416 | |||||||
| chr2:181035480 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.246-22213T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035480 | |||||||
| chr2:181035497 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-22196A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035497 | |||||||
| chr2:181035509 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.246-22184T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035509 | |||||||
| chr2:181035559 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-22134G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035559 | |||||||
| chr2:181035582 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-22111A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035582 | |||||||
| chr2:181035619 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.246-22074C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035619 | |||||||
| chr2:181035674 | A | T | 1 | a0001c0001t0006g0035 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.246-22019A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035674 | |||||||
| chr2:181035689 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-22004C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035689 | |||||||
| chr2:181035727 | T | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-21966T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035727 | |||||||
| chr2:181035746 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.246-21947A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035746 | |||||||
| chr2:181035782 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-21911T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035782 | |||||||
| chr2:181035798 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0003g0008 |
2 | HG01243.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.246-21895T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035798 | |||||||
| chr2:181035802 | C | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0307 |
2 | HG00423.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.246-21891C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035802 | |||||||
| chr2:181035841 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.246-21852A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035841 | |||||||
| chr2:181035895 | C | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-21798C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035895 | |||||||
| chr2:181035936 | AG | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-21755delG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181035936 | ||||||
| chr2:181035986 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0103 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.246-21707C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181035986 | |||||||
| chr2:181036223 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02622.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.246-21470G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036223 | |||||||
| chr2:181036294 | T | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(22): Show |
29 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.246-21399T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036294 | |||||||
| chr2:181036471 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.246-21222C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036471 | |||||||
| chr2:181036499 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.246-21194C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036499 | |||||||
| chr2:181036718 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.246-20975A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036718 | |||||||
| chr2:181036748 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.246-20945T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036748 | |||||||
| chr2:181036853 | T | G | 1 | a0001c0001t0002g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.246-20840T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036853 | |||||||
| chr2:181036856 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246-20837G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036856 | |||||||
| chr2:181036961 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.246-20732C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181036961 | |||||||
| chr2:181037044 | A | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-20649A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037044 | |||||||
| chr2:181037125 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246-20568G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037125 | |||||||
| chr2:181037178 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.246-20515A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037178 | |||||||
| chr2:181037194 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.246-20499A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037194 | |||||||
| chr2:181037198 | A | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-20495A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037198 | |||||||
| chr2:181037202 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-20491T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037202 | |||||||
| chr2:181037264 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-20429A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037264 | |||||||
| chr2:181037338 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0003g0231 |
2 | HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.246-20355T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037338 | |||||||
| chr2:181037432 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-20261G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037432 | |||||||
| chr2:181037526 | T | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-20167T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037526 | |||||||
| chr2:181037706 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.246-19987A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037706 | |||||||
| chr2:181037735 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-19958A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037735 | |||||||
| chr2:181037742 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-19951G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037742 | |||||||
| chr2:181037744 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-19949G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037744 | |||||||
| chr2:181037832 | G | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0236 a0001c0001t0001g0248 |
3 | NA18951.hp2 NA18983.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.246-19861G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037832 | |||||||
| chr2:181037861 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.246-19832G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181037861 | |||||||
| chr2:181038094 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.246-19599C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038094 | |||||||
| chr2:181038287 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-19406G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038287 | |||||||
| chr2:181038291 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-19402G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038291 | |||||||
| chr2:181038351 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.246-19342A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038351 | |||||||
| chr2:181038370 | C | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-19323C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038370 | |||||||
| chr2:181038441 | A | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0219 |
2 | NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.246-19252A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038441 | |||||||
| chr2:181038585 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.246-19108C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038585 | |||||||
| chr2:181038607 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-19086G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038607 | |||||||
| chr2:181038689 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.246-19004C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038689 | |||||||
| chr2:181038716 | GCAAGTCT others(7): Show |
G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0195 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.246-18967_246-1895 others(18): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181038716 | ||||||
| chr2:181038776 | G | T | 1 | a0001c0001t0002g0015 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.246-18917G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038776 | |||||||
| chr2:181038814 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.246-18879A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181038814 | |||||||
| chr2:181039123 | C | CT | 9 | a0001c0001t0001g0021 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00408.hp1 HG01978.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-18545dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181039123 | ||||||
| chr2:181039123 | CT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.246-18545delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181039123 | ||||||
| chr2:181039123 | CTT | C | 54 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(51): Show |
56 | HG00544.hp1 HG00558.hp2 HG01516.hp2 others(53): Show |
intron_variant | MODIFIER | c.246-18546_246-1854 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181039123 | ||||||
| chr2:181039123 | CTTT | C | 8 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0001g0165 others(5): Show |
8 | HG01074.hp1 HG02735.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-18547_246-1854 others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181039123 | ||||||
| chr2:181039151 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-18542A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039151 | |||||||
| chr2:181039237 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
224 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.246-18456A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039237 | |||||||
| chr2:181039281 | TA | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-18409delA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181039281 | ||||||
| chr2:181039283 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-18410A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039283 | |||||||
| chr2:181039284 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-18409A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039284 | |||||||
| chr2:181039286 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-18407T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039286 | |||||||
| chr2:181039431 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.246-18262G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039431 | |||||||
| chr2:181039432 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.246-18261A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039432 | |||||||
| chr2:181039589 | G | C | 1 | a0001c0001t0001g0295 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.246-18104G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039589 | |||||||
| chr2:181039633 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.246-18060A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039633 | |||||||
| chr2:181039641 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.246-18052T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039641 | |||||||
| chr2:181039650 | AT | A | 47 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0024 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.246-18040delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181039650 | ||||||
| chr2:181039677 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-18016G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039677 | |||||||
| chr2:181039694 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-17999A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039694 | |||||||
| chr2:181039744 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(62): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.246-17949G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039744 | |||||||
| chr2:181039758 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246-17935C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039758 | |||||||
| chr2:181039904 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0150 others(17): Show |
20 | HG01981.hp2 HG02056.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.246-17789A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181039904 | |||||||
| chr2:181040191 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.246-17502G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040191 | |||||||
| chr2:181040439 | T | G | 3 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0001t0002g0144 |
3 | HG00140.hp2 HG01169.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.246-17254T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040439 | |||||||
| chr2:181040481 | T | C | 1 | a0001c0001t0003g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.246-17212T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040481 | |||||||
| chr2:181040627 | C | A | 35 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0063 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.246-17066C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040627 | |||||||
| chr2:181040648 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.246-17045G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040648 | |||||||
| chr2:181040713 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.246-16980A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040713 | |||||||
| chr2:181040835 | G | C | 1 | a0001c0001t0005g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.246-16858G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040835 | |||||||
| chr2:181040896 | T | G | 40 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
41 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(38): Show |
intron_variant | MODIFIER | c.246-16797T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040896 | |||||||
| chr2:181040917 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-16776G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040917 | |||||||
| chr2:181040924 | C | CG | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-16769_246-1676 others(5): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040924 | |||||||
| chr2:181040927 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-16766A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040927 | |||||||
| chr2:181040943 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-16750C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181040943 | |||||||
| chr2:181041020 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.246-16673C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041020 | |||||||
| chr2:181041032 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG00733.hp1 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.246-16661G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041032 | |||||||
| chr2:181041157 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.246-16536A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041157 | |||||||
| chr2:181041230 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.246-16463G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041230 | |||||||
| chr2:181041232 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0003 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.246-16461_246-1646 others(14): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041232 | |||||||
| chr2:181041232 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0018 a0001c0001t0002g0055 a0001c0001t0006g0035 |
3 | HG02615.hp1 HG02738.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.246-16461_246-1646 others(15): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041232 | |||||||
| chr2:181041232 | C | CAAAAAAA others(5): Show |
30 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(27): Show |
30 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.246-16461_246-1646 others(16): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041232 | |||||||
| chr2:181041232 | C | CAAAAAAA others(6): Show |
15 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0032 others(12): Show |
15 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.246-16461_246-1646 others(17): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041232 | |||||||
| chr2:181041232 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0002g0031 a0001c0001t0002g0038 |
2 | HG00609.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.246-16461_246-1646 others(18): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041232 | |||||||
| chr2:181041232 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0026 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.246-16461_246-1646 others(19): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041232 | |||||||
| chr2:181041233 | T | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.246-16460T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041233 | |||||||
| chr2:181041234 | C | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.246-16459C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041234 | |||||||
| chr2:181041234 | C | CA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
181 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.246-16440dupA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181041234 | ||||||
| chr2:181041234 | C | CAA | 41 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0130 others(38): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.246-16441_246-1644 others(6): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181041234 | ||||||
| chr2:181041259 | A | AT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
10 | HG00544.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.246-16424dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181041259 | ||||||
| chr2:181041357 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.246-16336T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041357 | |||||||
| chr2:181041384 | A | G | 40 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
41 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(38): Show |
intron_variant | MODIFIER | c.246-16309A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041384 | |||||||
| chr2:181041447 | A | AT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
55 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.246-16235dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181041447 | ||||||
| chr2:181041499 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.246-16194G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041499 | |||||||
| chr2:181041536 | C | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.246-16157C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041536 | |||||||
| chr2:181041643 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-16050G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041643 | |||||||
| chr2:181041663 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.246-16030C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041663 | |||||||
| chr2:181041678 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18977.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.246-16015C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041678 | |||||||
| chr2:181041705 | GGATT | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-15983_246-1598 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181041705 | ||||||
| chr2:181041761 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-15932T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041761 | |||||||
| chr2:181041782 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.246-15911T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041782 | |||||||
| chr2:181041828 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-15865T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181041828 | |||||||
| chr2:181042166 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.246-15527A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042166 | |||||||
| chr2:181042271 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.246-15422G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042271 | |||||||
| chr2:181042371 | A | T | 12 | a0001c0001t0001g0059 a0001c0001t0001g0127 a0001c0001t0001g0184 others(9): Show |
12 | HG01175.hp1 HG02015.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.246-15322A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042371 | |||||||
| chr2:181042410 | A | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(37): Show |
44 | HG00423.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.246-15283A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042410 | |||||||
| chr2:181042833 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0128 others(11): Show |
15 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.246-14860A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042833 | |||||||
| chr2:181042885 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-14808G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042885 | |||||||
| chr2:181042890 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.246-14803A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042890 | |||||||
| chr2:181042998 | A | G | 43 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0063 others(40): Show |
43 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.246-14695A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181042998 | |||||||
| chr2:181043312 | A | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0165 others(4): Show |
7 | NA18962.hp2 NA18973.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.246-14381A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043312 | |||||||
| chr2:181043410 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-14283A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043410 | |||||||
| chr2:181043598 | A | C | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246-14095A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043598 | |||||||
| chr2:181043669 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.246-14024G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043669 | |||||||
| chr2:181043686 | TAATC | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0324 |
3 | HG01891.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246-14003_246-1400 others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181043686 | ||||||
| chr2:181043710 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.246-13983C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043710 | |||||||
| chr2:181043711 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-13982T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043711 | |||||||
| chr2:181043860 | A | G | 6 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.246-13833A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181043860 | |||||||
| chr2:181044009 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.246-13684T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044009 | |||||||
| chr2:181044137 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-13556A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044137 | |||||||
| chr2:181044191 | T | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-13502T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044191 | |||||||
| chr2:181044246 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-13447A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044246 | |||||||
| chr2:181044363 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(22): Show |
29 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.246-13330A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044363 | |||||||
| chr2:181044512 | C | T | 1 | a0001c0001t0005g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.246-13181C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044512 | |||||||
| chr2:181044700 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.246-12993T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044700 | |||||||
| chr2:181044704 | G | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-12989G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044704 | |||||||
| chr2:181044709 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.246-12984C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044709 | |||||||
| chr2:181044724 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(37): Show |
intron_variant | MODIFIER | c.246-12969A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044724 | |||||||
| chr2:181044767 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.246-12926A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181044767 | |||||||
| chr2:181045024 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.246-12669T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045024 | |||||||
| chr2:181045237 | T | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-12456T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045237 | |||||||
| chr2:181045282 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-12411A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045282 | |||||||
| chr2:181045326 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-12367G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045326 | |||||||
| chr2:181045330 | C | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(19): Show |
25 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.246-12363C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045330 | |||||||
| chr2:181045655 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0301 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-12038T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045655 | |||||||
| chr2:181045785 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.246-11908C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181045785 | |||||||
| chr2:181045879 | G | GA | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-11804dupA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181045879 | ||||||
| chr2:181046047 | T | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
224 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.246-11646T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046047 | |||||||
| chr2:181046093 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.246-11600C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046093 | |||||||
| chr2:181046155 | A | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-11538A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046155 | |||||||
| chr2:181046156 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.246-11537G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046156 | |||||||
| chr2:181046161 | A | C | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-11532A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046161 | |||||||
| chr2:181046165 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.246-11528A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046165 | |||||||
| chr2:181046234 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.246-11459G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046234 | |||||||
| chr2:181046464 | C | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-11229C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046464 | |||||||
| chr2:181046562 | T | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-11131T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046562 | |||||||
| chr2:181046762 | T | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(124): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.246-10931T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046762 | |||||||
| chr2:181046944 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-10749A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181046944 | |||||||
| chr2:181047080 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-10613G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047080 | |||||||
| chr2:181047303 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.246-10390G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047303 | |||||||
| chr2:181047433 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.246-10260T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047433 | |||||||
| chr2:181047584 | C | CT | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-10105dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181047584 | ||||||
| chr2:181047674 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-10019C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047674 | |||||||
| chr2:181047695 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246-9998A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047695 | |||||||
| chr2:181047792 | T | TGAG | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-9896_246-9894d others(5): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181047792 | ||||||
| chr2:181047854 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG01074.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.246-9839T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047854 | |||||||
| chr2:181047952 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.246-9741C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181047952 | |||||||
| chr2:181047953 | G | GT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-9737dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181047953 | ||||||
| chr2:181048048 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246-9645C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048048 | |||||||
| chr2:181048088 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.246-9605A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048088 | |||||||
| chr2:181048088 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.246-9605A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048088 | |||||||
| chr2:181048264 | T | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-9429T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048264 | |||||||
| chr2:181048284 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.246-9409T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048284 | |||||||
| chr2:181048313 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(61): Show |
69 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.246-9380C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048313 | |||||||
| chr2:181048322 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-9371A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048322 | |||||||
| chr2:181048395 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-9298A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048395 | |||||||
| chr2:181048471 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00642.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.246-9222G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048471 | |||||||
| chr2:181048500 | G | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-9193G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048500 | |||||||
| chr2:181048515 | T | G | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0286 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-9178T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048515 | |||||||
| chr2:181048662 | AT | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-9029delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181048662 | ||||||
| chr2:181048791 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0324 |
3 | HG01891.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246-8902C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048791 | |||||||
| chr2:181048937 | C | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-8756C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181048937 | |||||||
| chr2:181049131 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.246-8562G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181049131 | |||||||
| chr2:181049277 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.246-8416A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181049277 | |||||||
| chr2:181049686 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-8007C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181049686 | |||||||
| chr2:181049696 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.246-7997C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181049696 | |||||||
| chr2:181050034 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-7659A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050034 | |||||||
| chr2:181050052 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.246-7641A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050052 | |||||||
| chr2:181050155 | C | CTTCTTTA others(4): Show |
1 | a0001c0001t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.246-7537_246-7527d others(13): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181050155 | ||||||
| chr2:181050162 | A | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0269 |
3 | HG01071.hp1 HG01496.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.246-7531A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050162 | |||||||
| chr2:181050170 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.246-7523A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050170 | |||||||
| chr2:181050172 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-7521A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050172 | |||||||
| chr2:181050183 | T | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-7510T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050183 | |||||||
| chr2:181050214 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-7479A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050214 | |||||||
| chr2:181050225 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.246-7468C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050225 | |||||||
| chr2:181050234 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.246-7459A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050234 | |||||||
| chr2:181050245 | A | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | NA18989.hp2 NA18993.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-7448A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050245 | |||||||
| chr2:181050251 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.246-7442A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050251 | |||||||
| chr2:181050323 | A | G | 5 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | NA18959.hp2 NA18969.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-7370A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050323 | |||||||
| chr2:181050423 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.246-7270T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050423 | |||||||
| chr2:181050496 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-7197A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050496 | |||||||
| chr2:181050676 | G | T | 2 | a0001c0001t0002g0023 a0001c0001t0006g0022 |
2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.246-7017G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050676 | |||||||
| chr2:181050965 | T | C | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(37): Show |
intron_variant | MODIFIER | c.246-6728T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181050965 | |||||||
| chr2:181051028 | C | T | 1 | a0001c0001t0009g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.246-6665C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051028 | |||||||
| chr2:181051032 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.246-6661C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051032 | |||||||
| chr2:181051076 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18977.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.246-6617C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051076 | |||||||
| chr2:181051091 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.246-6602A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051091 | |||||||
| chr2:181051119 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0172 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.246-6574C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051119 | |||||||
| chr2:181051218 | A | T | 1 | a0001c0001t0009g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.246-6475A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051218 | |||||||
| chr2:181051688 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-6005G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051688 | |||||||
| chr2:181051891 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.246-5802G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051891 | |||||||
| chr2:181051937 | C | T | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-5756C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181051937 | |||||||
| chr2:181052000 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.246-5693G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052000 | |||||||
| chr2:181052035 | T | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-5658T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052035 | |||||||
| chr2:181052066 | G | GTGC | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-5625_246-5624i others(5): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181052066 | ||||||
| chr2:181052071 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0322 |
3 | HG01081.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.246-5622G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052071 | |||||||
| chr2:181052116 | C | T | 2 | a0001c0001t0005g0124 a0001c0001t0005g0125 |
2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.246-5577C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052116 | |||||||
| chr2:181052127 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-5566G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052127 | |||||||
| chr2:181052274 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.246-5419C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052274 | |||||||
| chr2:181052341 | C | CTTCATCC others(1): Show |
6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-5352_246-5351i others(10): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052341 | |||||||
| chr2:181052626 | A | AT | 39 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(36): Show |
41 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(38): Show |
intron_variant | MODIFIER | c.246-5063dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181052626 | ||||||
| chr2:181052729 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.246-4964A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052729 | |||||||
| chr2:181052817 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.246-4876T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181052817 | |||||||
| chr2:181053027 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.246-4666A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053027 | |||||||
| chr2:181053034 | A | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-4659A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053034 | |||||||
| chr2:181053082 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.246-4611G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053082 | |||||||
| chr2:181053160 | A | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-4533A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053160 | |||||||
| chr2:181053319 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.246-4374A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053319 | |||||||
| chr2:181053420 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0273 |
3 | HG02071.hp2 HG02080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.246-4273A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053420 | |||||||
| chr2:181053473 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.246-4220A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053473 | |||||||
| chr2:181053477 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.246-4216A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053477 | |||||||
| chr2:181053599 | A | ATC | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-4090_246-4089d others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181053599 | ||||||
| chr2:181053717 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.246-3976C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053717 | |||||||
| chr2:181053791 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.246-3902G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053791 | |||||||
| chr2:181053793 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.246-3900C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053793 | |||||||
| chr2:181053950 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.246-3743A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181053950 | |||||||
| chr2:181054029 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-3664T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054029 | |||||||
| chr2:181054169 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.246-3524A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054169 | |||||||
| chr2:181054321 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0001g0178 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.246-3372T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054321 | |||||||
| chr2:181054668 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
40 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(37): Show |
intron_variant | MODIFIER | c.246-3025A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054668 | |||||||
| chr2:181054693 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.246-3000G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054693 | |||||||
| chr2:181054763 | G | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-2930G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054763 | |||||||
| chr2:181054891 | A | G | 1 | a0001c0001t0003g0196 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.246-2802A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181054891 | |||||||
| chr2:181055052 | T | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-2641T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055052 | |||||||
| chr2:181055225 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.246-2468G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055225 | |||||||
| chr2:181055241 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.246-2452A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055241 | |||||||
| chr2:181055402 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-2291C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055402 | |||||||
| chr2:181055495 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.246-2198T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055495 | |||||||
| chr2:181055504 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.246-2189G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055504 | |||||||
| chr2:181055538 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.246-2155G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055538 | |||||||
| chr2:181055611 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-2082A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055611 | |||||||
| chr2:181055634 | A | G | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-2059A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055634 | |||||||
| chr2:181055671 | AATAGTTA others(17): Show |
A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-1998_246-1975d others(26): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181055671 | ||||||
| chr2:181055682 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.246-2011G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055682 | |||||||
| chr2:181055749 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.246-1944A>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055749 | |||||||
| chr2:181055830 | T | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-1863T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181055830 | |||||||
| chr2:181056001 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246-1692G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056001 | |||||||
| chr2:181056035 | T | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-1658T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056035 | |||||||
| chr2:181056036 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-1657T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056036 | |||||||
| chr2:181056081 | TA | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.246-1594delA | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181056081 | ||||||
| chr2:181056081 | TAA | T | 9 | a0001c0001t0001g0130 a0001c0001t0001g0157 a0001c0001t0001g0210 others(6): Show |
9 | HG02040.hp1 HG03041.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.246-1595_246-1594d others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181056081 | ||||||
| chr2:181056132 | T | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): Show |
8 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.246-1561T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056132 | |||||||
| chr2:181056542 | G | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
31 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246-1151G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056542 | |||||||
| chr2:181056690 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-1003G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056690 | |||||||
| chr2:181056936 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.246-757T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056936 | |||||||
| chr2:181056952 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-741C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056952 | |||||||
| chr2:181056970 | A | G | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-723A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056970 | |||||||
| chr2:181056974 | G | A | 1 | a0001c0001t0009g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.246-719G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056974 | |||||||
| chr2:181056996 | G | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0105 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.246-697G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181056996 | |||||||
| chr2:181057000 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-693C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181057000 | |||||||
| chr2:181057191 | G | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.246-502G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181057191 | |||||||
| chr2:181057199 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.246-494T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181057199 | |||||||
| chr2:181057272 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.246-421A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181057272 | |||||||
| chr2:181057287 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.246-406G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | chr2 | 181057287 | |||||||
| chr2:181057388 | A | AG | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-304dupG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 181057388 | ||||||
| chr2:181058107 | T | A | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.378+282T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058107 | |||||||
| chr2:181058110 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.378+285A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058110 | |||||||
| chr2:181058111 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.378+286C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058111 | |||||||
| chr2:181058112 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.378+287C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058112 | |||||||
| chr2:181058193 | T | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.378+368T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058193 | |||||||
| chr2:181058226 | T | G | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.378+401T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058226 | |||||||
| chr2:181058327 | T | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+502T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058327 | |||||||
| chr2:181058339 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.378+514G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058339 | |||||||
| chr2:181058399 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.378+574G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058399 | |||||||
| chr2:181058461 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.378+636T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058461 | |||||||
| chr2:181058726 | GTA | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.378+905_378+906del others(2): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 181058726 | ||||||
| chr2:181058749 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.378+924C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058749 | |||||||
| chr2:181058794 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0237 |
3 | HG00738.hp2 HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.378+969T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058794 | |||||||
| chr2:181058983 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0193 others(2): Show |
7 | HG01891.hp1 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+1158C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058983 | |||||||
| chr2:181058986 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.378+1161C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181058986 | |||||||
| chr2:181059046 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.378+1221T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059046 | |||||||
| chr2:181059055 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.378+1230G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059055 | |||||||
| chr2:181059158 | T | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
39 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.378+1333T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059158 | |||||||
| chr2:181059568 | C | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.379-1097C>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059568 | |||||||
| chr2:181059597 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.379-1068C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059597 | |||||||
| chr2:181059624 | T | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.379-1041T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059624 | |||||||
| chr2:181059827 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.379-838T>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059827 | |||||||
| chr2:181059866 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.379-799C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059866 | |||||||
| chr2:181059873 | A | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
39 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.379-792A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059873 | |||||||
| chr2:181059917 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.379-748C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059917 | |||||||
| chr2:181059928 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.379-737A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059928 | |||||||
| chr2:181059947 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.379-718A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181059947 | |||||||
| chr2:181060125 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.379-540A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181060125 | |||||||
| chr2:181060263 | T | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
30 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.379-402T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181060263 | |||||||
| chr2:181060272 | A | AG | 6 | a0001c0001t0005g0122 a0001c0001t0005g0123 a0001c0001t0005g0124 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-393_379-392ins others(1): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181060272 | |||||||
| chr2:181060314 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.379-351T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181060314 | |||||||
| chr2:181060338 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379-327T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181060338 | |||||||
| chr2:181060510 | A | G | 1 | a0001c0001t0001g0006 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.379-155A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 4/5 | chr2 | 181060510 | |||||||
| chr2:181060861 | C | CT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0056 others(11): Show |
15 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+76dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060861 | ||||||
| chr2:181060861 | CT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(52): Show |
58 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.526+76delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060861 | ||||||
| chr2:181060861 | CTT | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.526+75_526+76delTT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060861 | ||||||
| chr2:181060861 | CTTT | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0128 others(10): Show |
14 | HG01070.hp2 HG01884.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.526+74_526+76delTT others(1): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060861 | ||||||
| chr2:181060861 | CTTTTTTT others(2): Show |
C | 34 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0063 others(31): Show |
34 | HG00408.hp1 HG00438.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.526+68_526+76delTT others(7): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060861 | ||||||
| chr2:181060861 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+67_526+76delTT others(8): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060861 | ||||||
| chr2:181060890 | GT | G | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+80delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060890 | ||||||
| chr2:181060910 | G | C | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+98G>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181060910 | |||||||
| chr2:181060929 | TAGAA | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+121_526+124del others(4): Show |
UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181060929 | ||||||
| chr2:181060987 | T | C | 37 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.526+175T>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181060987 | |||||||
| chr2:181061058 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(61): Show |
69 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.526+246A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061058 | |||||||
| chr2:181061100 | AGACCACT others(315): Show |
A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.526+299_526+620del | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181061100 | ||||||
| chr2:181061423 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0086 |
2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526+611G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061423 | |||||||
| chr2:181061442 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.526+630A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061442 | |||||||
| chr2:181061505 | AG | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.526+695delG | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181061505 | ||||||
| chr2:181061638 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.526+826C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061638 | |||||||
| chr2:181061650 | C | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
30 | HG00423.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.526+838C>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061650 | |||||||
| chr2:181061710 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.526+898G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061710 | |||||||
| chr2:181061775 | CT | C | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
193 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.526+977delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181061775 | ||||||
| chr2:181061839 | T | A | 1 | a0001c0001t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.527-952T>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181061839 | |||||||
| chr2:181062050 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02717.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.527-741C>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062050 | |||||||
| chr2:181062175 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-616G>A | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062175 | |||||||
| chr2:181062175 | G | GT | 38 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
39 | HG00544.hp1 HG00558.hp2 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.527-607dupT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181062175 | ||||||
| chr2:181062245 | A | C | 7 | a0001c0001t0001g0323 a0001c0001t0005g0122 a0001c0001t0005g0123 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-546A>C | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062245 | |||||||
| chr2:181062290 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-501A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062290 | |||||||
| chr2:181062468 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.527-323A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062468 | |||||||
| chr2:181062583 | AT | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.527-197delT | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 181062583 | ||||||
| chr2:181062616 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.527-175G>T | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062616 | |||||||
| chr2:181062633 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.527-158A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062633 | |||||||
| chr2:181062635 | A | G | 1 | a0001c0001t0003g0268 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.527-156A>G | UBE2E3 | ENSG00000170035.16 | transcript | ENST00000410062.9 | protein_coding | 5/5 | chr2 | 181062635 |