Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 997 |
| ensemblid | ENSG00000099804.9 |
| hgncid | 1734 |
| symbol | CDC34 |
| name | cell division cycle 34, ubiqiutin conjugating enzyme |
| refseq_nuc | NM_004359.2 |
| refseq_prot | NP_004350.1 |
| ensembl_nuc | ENST00000215574.9 |
| ensembl_prot | ENSP00000215574.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 531760 |
| end | 542087 |
| strand | + |
| ver | v1.2 |
| region | chr19:531760-542087 |
| region5000 | chr19:526760-547087 |
| regionname0 | CDC34_chr19_531760_542087 |
| regionname5000 | CDC34_chr19_526760_547087 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 236 | 327 | 86 | 62 | 131 | 14 | 32 | 100 | CDC34_chr19_526760_547087 | CDC34 | MARPL others(231): Show |
chr19 | 526760 | 547087 |
| a0002 | 0/0 | 236 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | MARPL others(231): Show |
chr19 | 526760 | 547087 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 708 | 301 | 81 | 58 | 120 | 13 | 27 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 | ||
| a0001c0002 | 0/0 | 708 | 21 | 4 | 3 | 10 | 1 | 3 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 | ||
| a0001c0003 | 0/0 | 708 | 2 | 0 | 1 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 | ||
| a0001c0005 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 | ||
| a0001c0006 | 0/0 | 708 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 | ||
| a0001c0007 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 | ||
| a0002c0004 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | ATGGC others(703): Show |
chr19 | 526760 | 547087 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1418 | 144 | 63 | 21 | 40 | 8 | 10 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0002 | 0/0 | 1418 | 133 | 2 | 36 | 73 | 5 | 17 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0003 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0004 | 0/0 | 1417 | 7 | 7 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1412): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0005 | 0/0 | 1418 | 6 | 6 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0007 | 0/0 | 1418 | 5 | 0 | 0 | 5 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0008 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0009 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0010 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0011 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0001t0012 | 0/0 | 1418 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0002t0003 | 0/0 | 1418 | 16 | 2 | 1 | 10 | 0 | 3 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0002t0006 | 0/0 | 1418 | 5 | 2 | 2 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0003t0001 | 0/0 | 1418 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0003t0002 | 0/0 | 1418 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0005t0002 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0006t0002 | 0/0 | 1418 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0001c0007t0002 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| a0002c0004t0002 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | AGAGC others(1413): Show |
chr19 | 526760 | 547087 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 18 | 0 | 3 | 13 | 2 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0004 | 0/0 | 10 | 5 | 3 | 1 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0006 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0001 | 0/0 | 29 | 0 | 3 | 18 | 2 | 6 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0002 | 0/0 | 24 | 0 | 2 | 18 | 1 | 3 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0022 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0005g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0007g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0001t0012g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0005 | 0/0 | 7 | 1 | 0 | 4 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0006g0017 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0002t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0005t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0006t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0001c0007t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| a0002c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00140 | hp1 | a0001 | c0002 | t0006 | g0017 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG00738 | hp2 | a0001 | c0002 | t0006 | g0077 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0120 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0096 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01884 | hp1 | a0001 | c0007 | t0002 | g0050 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01975 | hp1 | a0001 | c0002 | t0006 | g0017 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0028 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02083 | hp1 | a0002 | c0004 | t0002 | g0142 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0017 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03130 | hp1 | a0001 | c0002 | t0006 | g0076 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03669 | hp2 | a0001 | c0006 | t0002 | g0025 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0031 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0121 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18960 | hp2 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18961 | hp1 | a0001 | c0005 | t0002 | g0154 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18964 | hp1 | a0001 | c0001 | t0008 | g0082 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18968 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19067 | hp1 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ASW | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | GIH | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | USA | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | USA | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0044 | REF | REF | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:535886 | G | A | 1 | a0002 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.227G>A | p.Arg76Gln | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/5 | 399/1418 | 227/711 | 76/236 | chr19 | 535886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:532066 | C | T | 1 | a0001c0002 | 21 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(18): Show |
synonymous_variant | LOW | c.135C>T | p.Ile45Ile | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 307/1418 | 135/711 | 45/236 | chr19 | 532066 | |||
| chr19:536335 | C | T | 1 | a0001c0007 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.357C>T | p.Asn119Asn | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/5 | 529/1418 | 357/711 | 119/236 | chr19 | 536335 | |||
| chr19:537046 | C | T | 1 | a0001c0003 | 2 | HG01074.hp2 HG03927.hp2 |
synonymous_variant | LOW | c.396C>T | p.Asn132Asn | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/5 | 568/1418 | 396/711 | 132/236 | chr19 | 537046 | |||
| chr19:541399 | G | A | 1 | a0001c0005 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.558G>A | p.Thr186Thr | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 730/1418 | 558/711 | 186/236 | chr19 | 541399 | |||
| chr19:541459 | C | T | 1 | a0001c0006 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.618C>T | p.Phe206Phe | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 790/1418 | 618/711 | 206/236 | chr19 | 541459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:531773 | C | T | 1 | a0001c0001t0012 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 159 | chr19 | 531773 | ||||||
| chr19:531791 | G | A | 1 | a0001c0001t0001 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 141 | chr19 | 531791 | ||||||
| chr19:531842 | C | G | 1 | a0001c0001t0011 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-90C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 90 | chr19 | 531842 | ||||||
| chr19:531891 | G | A | 1 | a0001c0001t0008 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 41 | chr19 | 531891 | ||||||
| chr19:541685 | C | T | 8 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(5): Show |
144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 133 | chr19 | 541685 | ||||||
| chr19:541689 | C | T | 1 | a0001c0001t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 137 | chr19 | 541689 | ||||||
| chr19:541770 | C | T | 1 | a0001c0001t0011 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 218 | chr19 | 541770 | ||||||
| chr19:541771 | G | A | 1 | a0001c0001t0007 | 5 | NA18968.hp1 NA18971.hp1 NA18983.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*219G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 219 | chr19 | 541771 | ||||||
| chr19:541788 | G | T | 1 | a0001c0001t0009 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 236 | chr19 | 541788 | ||||||
| chr19:541917 | C | T | 1 | a0001c0002t0006 | 5 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*365C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 365 | chr19 | 541917 | ||||||
| chr19:541958 | AG | A | 1 | a0001c0001t0004 | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*410delG | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 410 | INFO_REALIGN_3_PRIME | chr19 | 541958 | |||||
| chr19:542009 | A | T | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0006 |
22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*457A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 457 | chr19 | 542009 | ||||||
| chr19:542077 | A | G | 1 | a0001c0001t0005 | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 525 | chr19 | 542077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:532184 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.177+76G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532184 | |||||||
| chr19:532268 | G | T | 4 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(1): Show |
4 | HG02735.hp1 HG03492.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+160G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532268 | |||||||
| chr19:532316 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+208G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532316 | |||||||
| chr19:532337 | C | T | 67 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0002g0001 others(64): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.177+229C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532337 | |||||||
| chr19:532347 | C | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.177+239C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532347 | |||||||
| chr19:532364 | C | A | 12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.177+256C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532364 | |||||||
| chr19:532437 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0011g0158 |
2 | NA18960.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.177+329C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532437 | |||||||
| chr19:532570 | C | T | 67 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0002g0001 others(64): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.177+462C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532570 | |||||||
| chr19:532575 | A | T | 10 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0043 others(7): Show |
13 | HG00642.hp1 HG01243.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+467A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532575 | |||||||
| chr19:532580 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+472C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532580 | |||||||
| chr19:532600 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.177+492G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532600 | |||||||
| chr19:532800 | A | G | 8 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+692A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532800 | |||||||
| chr19:532918 | C | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0058 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+810C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532918 | |||||||
| chr19:532928 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.177+820G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532928 | |||||||
| chr19:532930 | C | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
59 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.177+822C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532930 | |||||||
| chr19:532937 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+829A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532937 | |||||||
| chr19:532948 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0033 others(4): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+840C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532948 | |||||||
| chr19:533006 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.177+898C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533006 | |||||||
| chr19:533025 | TTTG | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
9 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+927_177+929del others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 533025 | ||||||
| chr19:533133 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.177+1025T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533133 | |||||||
| chr19:533201 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
99 | HG00408.hp2 HG00544.hp2 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.177+1093G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533201 | |||||||
| chr19:533269 | A | T | 1 | a0001c0005t0002g0154 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.177+1161A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533269 | |||||||
| chr19:533314 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0039 a0001c0001t0002g0113 others(5): Show |
14 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+1206G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533314 | |||||||
| chr19:533374 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+1266A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533374 | |||||||
| chr19:533393 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.177+1285C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533393 | |||||||
| chr19:533395 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.177+1287C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533395 | |||||||
| chr19:533497 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.177+1389G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533497 | |||||||
| chr19:533519 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.177+1411G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533519 | |||||||
| chr19:533552 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.177+1444C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533552 | |||||||
| chr19:533677 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.177+1569A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533677 | |||||||
| chr19:533732 | C | T | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+1624C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533732 | |||||||
| chr19:533872 | G | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.177+1764G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533872 | |||||||
| chr19:533961 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.177+1853C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533961 | |||||||
| chr19:533962 | T | G | 1 | a0001c0001t0002g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.177+1854T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533962 | |||||||
| chr19:533986 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178-1851C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533986 | |||||||
| chr19:534062 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178-1775G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534062 | |||||||
| chr19:534096 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.178-1741T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534096 | |||||||
| chr19:534126 | G | A | 2 | a0001c0003t0001g0121 a0001c0003t0002g0120 |
2 | HG01074.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-1711G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534126 | |||||||
| chr19:534263 | T | C | 68 | a0001c0001t0001g0150 a0001c0001t0002g0001 a0001c0001t0002g0002 others(65): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.178-1574T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534263 | |||||||
| chr19:534350 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
56 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.178-1487C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534350 | |||||||
| chr19:534365 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-1472A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534365 | |||||||
| chr19:534366 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-1471A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534366 | |||||||
| chr19:534401 | A | AATCCAAG others(37): Show |
11 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(8): Show |
17 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-1422_178-1379d others(46): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534401 | ||||||
| chr19:534401 | A | AATCCAAG others(82): Show |
12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0046 others(9): Show |
18 | HG00408.hp2 HG02080.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-1377_178-1376i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534401 | ||||||
| chr19:534401 | A | AATCCAAG others(127): Show |
3 | a0001c0002t0006g0017 a0001c0002t0006g0076 a0001c0002t0006g0077 |
5 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-1377_178-1376i others(136): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534401 | ||||||
| chr19:534411 | C | CCCCGAGT others(82): Show |
17 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(14): Show |
54 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.178-1377_178-1376i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534411 | ||||||
| chr19:534411 | C | CCCCGAGT others(438): Show |
1 | a0001c0001t0001g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-1419_178-1418i others(447): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534411 | ||||||
| chr19:534411 | C | CCCCGAGT others(215): Show |
1 | a0001c0001t0012g0096 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.178-1419_178-1418i others(224): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534411 | ||||||
| chr19:534419 | A | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1418A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534419 | |||||||
| chr19:534420 | C | T | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1417C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534420 | |||||||
| chr19:534426 | C | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1411C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534426 | |||||||
| chr19:534434 | A | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1403A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534434 | |||||||
| chr19:534458 | CTGAGTGC others(39): Show |
C | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1378_178-1333d others(48): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534458 | |||||||
| chr19:534459 | T | TGTATGCC others(37): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01517.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.178-1377_178-1376i others(46): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534459 | ||||||
| chr19:534461 | A | T | 10 | a0001c0001t0001g0061 a0001c0002t0003g0005 a0001c0002t0003g0031 others(7): Show |
17 | HG02129.hp1 HG02300.hp2 HG03486.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-1376A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534461 | |||||||
| chr19:534462 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0002t0003g0005 others(8): Show |
18 | HG01243.hp2 HG02129.hp1 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.178-1375G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534462 | |||||||
| chr19:534464 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01517.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.178-1373G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534464 | |||||||
| chr19:534484 | A | ACCCACGA others(38): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(8): Show |
24 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.178-1332_178-1331i others(47): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534484 | ||||||
| chr19:534484 | A | G | 12 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0001t0001g0098 others(9): Show |
19 | HG01517.hp2 HG02129.hp1 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-1353A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534484 | |||||||
| chr19:534499 | C | CCCCCGAG others(36): Show |
1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.178-1334_178-1333i others(45): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534499 | ||||||
| chr19:534504 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.178-1333T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534504 | |||||||
| chr19:534506 | A | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.178-1331A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534506 | |||||||
| chr19:534507 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.178-1330G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534507 | |||||||
| chr19:534516 | C | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1321C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534516 | |||||||
| chr19:534524 | A | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1313A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534524 | |||||||
| chr19:534529 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1308G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534529 | |||||||
| chr19:534535 | A | G | 86 | a0001c0001t0001g0061 a0001c0001t0001g0093 a0001c0001t0001g0094 others(83): Show |
172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.178-1302A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534535 | |||||||
| chr19:534544 | CCCCCGAG others(80): Show |
C | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1288_178-1202d others(89): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534544 | ||||||
| chr19:534550 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1287A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534550 | |||||||
| chr19:534551 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1286G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534551 | |||||||
| chr19:534553 | A | ACCCTCCC others(37): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-1280_178-1237d others(46): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534553 | ||||||
| chr19:534553 | A | ACCCTCCC others(171): Show |
8 | a0001c0002t0003g0005 a0001c0002t0003g0031 a0001c0002t0003g0070 others(5): Show |
15 | HG02300.hp2 HG03486.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-1273_178-1272i others(180): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534553 | ||||||
| chr19:534553 | A | G | 5 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0002t0006g0017 others(2): Show |
7 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1284A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534553 | |||||||
| chr19:534565 | A | C | 69 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0001t0002g0001 others(66): Show |
148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.178-1272A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534565 | |||||||
| chr19:534568 | G | A | 69 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0001t0002g0001 others(66): Show |
148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.178-1269G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534568 | |||||||
| chr19:534568 | G | GCCTCGCC others(82): Show |
1 | a0001c0001t0001g0003 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.178-1245_178-1244i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534568 | ||||||
| chr19:534568 | G | GCCTCGCC others(81): Show |
33 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(30): Show |
71 | HG00408.hp2 HG00544.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.178-1237_178-1236i others(90): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534568 | ||||||
| chr19:534568 | G | GCCTCGCC others(125): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0003g0105 |
10 | HG01169.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-1237_178-1236i others(134): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534568 | ||||||
| chr19:534579 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1258G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534579 | |||||||
| chr19:534592 | C | CT | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(64): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.178-1245_178-1244i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534592 | |||||||
| chr19:534592 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.178-1245C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534592 | |||||||
| chr19:534601 | G | GCCCTGTC others(567): Show |
1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178-1134_178-1133i others(576): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534601 | ||||||
| chr19:534601 | G | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178-1236G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534601 | |||||||
| chr19:534609 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0099 others(1): Show |
7 | HG00099.hp1 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1228C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534609 | |||||||
| chr19:534612 | A | ACCTCACC others(82): Show |
1 | a0001c0002t0003g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.178-1221_178-1220i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534612 | ||||||
| chr19:534612 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0099 others(1): Show |
7 | HG00099.hp1 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1225A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534612 | |||||||
| chr19:534617 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1220G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534617 | |||||||
| chr19:534636 | C | CT | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1201_178-1200i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534636 | |||||||
| chr19:534636 | C | T | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1201C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534636 | |||||||
| chr19:534638 | A | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1199A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534638 | |||||||
| chr19:534639 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1198G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534639 | |||||||
| chr19:534653 | C | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(64): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.178-1184C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534653 | |||||||
| chr19:534656 | A | G | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(64): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.178-1181A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534656 | |||||||
| chr19:534667 | G | A | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1170G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534667 | |||||||
| chr19:534680 | C | CT | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1157_178-1156i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534680 | |||||||
| chr19:534685 | G | A | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1152G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534685 | |||||||
| chr19:534689 | T | TCCCTGTC others(169): Show |
1 | a0001c0001t0001g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.178-1017_178-1016i others(178): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534689 | ||||||
| chr19:534689 | T | TCCCTGTC others(169): Show |
10 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(7): Show |
23 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.178-1128_178-1127i others(178): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534689 | ||||||
| chr19:534697 | C | A | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1140C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534697 | |||||||
| chr19:534700 | A | G | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1137A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534700 | |||||||
| chr19:534710 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.178-1127C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534710 | |||||||
| chr19:534711 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1126G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534711 | |||||||
| chr19:534729 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1108G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534729 | |||||||
| chr19:534733 | T | G | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1104T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534733 | |||||||
| chr19:534741 | C | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1096C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534741 | |||||||
| chr19:534744 | A | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1093A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534744 | |||||||
| chr19:534777 | T | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1060T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534777 | |||||||
| chr19:534798 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.178-1039T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534798 | |||||||
| chr19:534821 | T | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02738.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.178-1016T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534821 | |||||||
| chr19:534843 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02738.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.178-994G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534843 | |||||||
| chr19:534852 | C | CCCCCGAG others(36): Show |
2 | a0001c0001t0001g0034 a0001c0001t0003g0105 |
3 | HG01169.hp2 HG02976.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.178-981_178-980ins others(43): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534852 | C | CCCCCGAG others(36): Show |
19 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(16): Show |
28 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(43): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534852 | C | CCCCCGAG others(80): Show |
15 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(12): Show |
45 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(87): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534852 | C | CCCCCGAG others(80): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0028 others(11): Show |
22 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(87): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534852 | C | CCCCCGAG others(124): Show |
1 | a0001c0001t0001g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178-981_178-980ins others(131): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534852 | C | CCCCCGAG others(388): Show |
1 | a0001c0001t0001g0014 | 4 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(395): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534852 | C | CCCCCGAG others(168): Show |
1 | a0001c0001t0001g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-981_178-980ins others(175): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | ||||||
| chr19:534856 | CT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0086 others(2): Show |
12 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-980delT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534856 | |||||||
| chr19:534857 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(50): Show |
104 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.178-980T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534857 | |||||||
| chr19:534874 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178-963C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534874 | |||||||
| chr19:534897 | C | CCCCCGAG others(36): Show |
1 | a0001c0001t0001g0029 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-936_178-935ins others(43): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534897 | ||||||
| chr19:534902 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-935T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534902 | |||||||
| chr19:535004 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
116 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-833T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535004 | |||||||
| chr19:535096 | C | T | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.178-741C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535096 | |||||||
| chr19:535104 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178-733A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535104 | |||||||
| chr19:535198 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-639A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535198 | |||||||
| chr19:535206 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.178-631C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535206 | |||||||
| chr19:535213 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.178-624G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535213 | |||||||
| chr19:535239 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178-598C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535239 | |||||||
| chr19:535277 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.178-560C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535277 | |||||||
| chr19:535304 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-533T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535304 | |||||||
| chr19:535321 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-516C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535321 | |||||||
| chr19:535322 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-515G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535322 | |||||||
| chr19:535332 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-505A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535332 | |||||||
| chr19:535333 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-504G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535333 | |||||||
| chr19:535342 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-495T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535342 | |||||||
| chr19:535349 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-488T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535349 | |||||||
| chr19:535351 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-486T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535351 | |||||||
| chr19:535352 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-485T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535352 | |||||||
| chr19:535354 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-483G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535354 | |||||||
| chr19:535358 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-479A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535358 | |||||||
| chr19:535360 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-477T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535360 | |||||||
| chr19:535361 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-476G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535361 | |||||||
| chr19:535362 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-475A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535362 | |||||||
| chr19:535363 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-474G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535363 | |||||||
| chr19:535365 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-472A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535365 | |||||||
| chr19:535366 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-471A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535366 | |||||||
| chr19:535366 | A | G | 1 | a0001c0001t0005g0008 | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-471A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535366 | |||||||
| chr19:535367 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-470T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535367 | |||||||
| chr19:535370 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-467T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535370 | |||||||
| chr19:535372 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-465T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535372 | |||||||
| chr19:535373 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-464G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535373 | |||||||
| chr19:535374 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-463T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535374 | |||||||
| chr19:535375 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-462G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535375 | |||||||
| chr19:535377 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-460T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535377 | |||||||
| chr19:535378 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-459A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535378 | |||||||
| chr19:535379 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-458A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535379 | |||||||
| chr19:535383 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-454T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535383 | |||||||
| chr19:535390 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-447A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535390 | |||||||
| chr19:535394 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-443T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535394 | |||||||
| chr19:535395 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-442G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535395 | |||||||
| chr19:535396 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-441G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535396 | |||||||
| chr19:535398 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-439T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535398 | |||||||
| chr19:535399 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-438G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535399 | |||||||
| chr19:535402 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-435A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535402 | |||||||
| chr19:535403 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-434A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535403 | |||||||
| chr19:535404 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-433G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535404 | |||||||
| chr19:535405 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-432G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535405 | |||||||
| chr19:535409 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-428T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535409 | |||||||
| chr19:535410 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-427G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535410 | |||||||
| chr19:535411 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-426G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535411 | |||||||
| chr19:535412 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-425A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535412 | |||||||
| chr19:535413 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-424G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535413 | |||||||
| chr19:535414 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-423G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535414 | |||||||
| chr19:535528 | C | G | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-309C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535528 | |||||||
| chr19:535535 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(6): Show |
20 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.178-302G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535535 | |||||||
| chr19:535594 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.178-243G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535594 | |||||||
| chr19:535621 | C | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
140 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.178-216C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535621 | |||||||
| chr19:535634 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(132): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.178-203G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535634 | |||||||
| chr19:535635 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.178-202G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535635 | |||||||
| chr19:535657 | G | A | 1 | a0001c0001t0001g0014 | 4 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-180G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535657 | |||||||
| chr19:535974 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.264+51T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 535974 | |||||||
| chr19:535999 | T | TTCCGGGA others(32): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0106 a0001c0001t0001g0155 |
4 | HG00642.hp1 HG03654.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+117_264+155dup others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 535999 | ||||||
| chr19:536014 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 |
6 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+91C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536014 | |||||||
| chr19:536038 | C | CTCCGGGA others(113): Show |
1 | a0001c0001t0001g0030 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.265-158_265-157ins others(120): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536038 | ||||||
| chr19:536046 | C | CCCGGGGC others(33): Show |
57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(54): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.265-158_265-157ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536046 | ||||||
| chr19:536067 | CGTCCTCG others(33): Show |
C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(7): Show |
23 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.265-153_265-114del others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536067 | ||||||
| chr19:536068 | G | A | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.264+145G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536068 | |||||||
| chr19:536068 | G | GTCCTCGT others(33): Show |
35 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(32): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.265-154_265-153ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536068 | ||||||
| chr19:536068 | G | GTCCTCGT others(33): Show |
7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-158_265-157ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536068 | ||||||
| chr19:536088 | C | CGGGGCGC others(33): Show |
39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.265-154_265-153ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536088 | ||||||
| chr19:536088 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(33): Show |
78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.265-155C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536088 | |||||||
| chr19:536107 | T | C | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-136T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536107 | |||||||
| chr19:536113 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.265-130C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536113 | |||||||
| chr19:536128 | C | T | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-115C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536128 | |||||||
| chr19:536178 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.265-65G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536178 | |||||||
| chr19:536363 | GTCCACCC others(32): Show |
G | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+34_362+72delAC others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr19 | 536363 | ||||||
| chr19:536400 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0140 |
2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.362+60G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536400 | |||||||
| chr19:536402 | A | C | 1 | a0001c0001t0002g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.362+62A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536402 | |||||||
| chr19:536426 | C | T | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.362+86C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536426 | |||||||
| chr19:536437 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.362+97A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536437 | |||||||
| chr19:536480 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.362+140C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536480 | |||||||
| chr19:536510 | A | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(68): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.362+170A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536510 | |||||||
| chr19:536527 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 |
6 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.362+187C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536527 | |||||||
| chr19:536536 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.362+196C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536536 | |||||||
| chr19:536545 | G | A | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.362+205G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536545 | |||||||
| chr19:536585 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG02486.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.362+245T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536585 | |||||||
| chr19:536610 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(138): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.362+270A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536610 | |||||||
| chr19:536610 | A | G | 2 | a0001c0001t0004g0051 a0001c0001t0004g0057 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.362+270A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536610 | |||||||
| chr19:536678 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.363-335G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536678 | |||||||
| chr19:536681 | T | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(69): Show |
151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.363-332T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536681 | |||||||
| chr19:536681 | T | G | 1 | a0001c0001t0002g0147 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.363-332T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536681 | |||||||
| chr19:536742 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(159): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.363-271T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536742 | |||||||
| chr19:536752 | G | A | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.363-261G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536752 | |||||||
| chr19:536878 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.363-135G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536878 | |||||||
| chr19:536900 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.363-113G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536900 | |||||||
| chr19:536935 | C | T | 1 | a0001c0001t0005g0008 | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-78C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536935 | |||||||
| chr19:536962 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.363-51G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536962 | |||||||
| chr19:537159 | C | CG | 5 | a0001c0001t0001g0083 a0001c0001t0002g0117 a0001c0001t0002g0146 others(2): Show |
5 | HG01099.hp1 HG01261.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+17dupG | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537159 | ||||||
| chr19:537159 | C | G | 1 | a0001c0001t0002g0147 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.497+12C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537159 | |||||||
| chr19:537159 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.497+12C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537159 | |||||||
| chr19:537229 | C | A | 1 | a0001c0001t0002g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.497+82C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537229 | |||||||
| chr19:537280 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+133G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537280 | |||||||
| chr19:537376 | A | G | 2 | a0001c0002t0003g0073 a0001c0002t0003g0074 |
2 | NA19000.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.497+229A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537376 | |||||||
| chr19:537397 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.497+250G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537397 | |||||||
| chr19:537400 | TGGAGTGC others(5): Show |
T | 1 | a0001c0002t0003g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.497+254_497+265del others(12): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537400 | |||||||
| chr19:537414 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+267G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537414 | |||||||
| chr19:537421 | C | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+274C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537421 | |||||||
| chr19:537453 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0028 others(9): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.497+306C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537453 | |||||||
| chr19:537598 | T | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.497+451T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537598 | |||||||
| chr19:537645 | G | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
94 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.497+498G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537645 | |||||||
| chr19:537647 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+500C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537647 | |||||||
| chr19:537651 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0021 others(18): Show |
33 | HG00408.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.497+525dupT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537651 | C | CTT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0027 others(12): Show |
27 | HG01099.hp2 HG01255.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.497+524_497+525dup others(2): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537651 | C | CTTTTTTT | 30 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0022 others(27): Show |
66 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.497+519_497+525dup others(7): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537651 | C | CTTTTTTT others(1): Show |
22 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(19): Show |
59 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.497+518_497+525dup others(8): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537651 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0002g0011 a0001c0001t0002g0039 a0001c0001t0002g0113 others(6): Show |
14 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+517_497+525dup others(9): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537651 | CT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0100 others(2): Show |
12 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+525delT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537651 | CTT | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
33 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.497+524_497+525del others(2): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | ||||||
| chr19:537676 | G | A | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.497+529G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537676 | |||||||
| chr19:537694 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.497+547T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537694 | |||||||
| chr19:537718 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+571C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537718 | |||||||
| chr19:538014 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497+867C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538014 | |||||||
| chr19:538015 | TTTAATGA others(61): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.497+936_497+1003de others(69): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 538015 | ||||||
| chr19:538034 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0103 |
2 | HG01192.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.497+887C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538034 | |||||||
| chr19:538098 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG02486.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.497+951G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538098 | |||||||
| chr19:538160 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.497+1013A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538160 | |||||||
| chr19:538169 | T | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(6): Show |
20 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.497+1022T>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538169 | |||||||
| chr19:538185 | C | T | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+1038C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538185 | |||||||
| chr19:538229 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02717.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.497+1082G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538229 | |||||||
| chr19:538230 | G | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0043 others(8): Show |
15 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.497+1083G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538230 | |||||||
| chr19:538289 | A | C | 1 | a0001c0001t0001g0018 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+1142A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538289 | |||||||
| chr19:538292 | G | A | 1 | a0001c0002t0003g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.497+1145G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538292 | |||||||
| chr19:538416 | C | T | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+1269C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538416 | |||||||
| chr19:538487 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+1340G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538487 | |||||||
| chr19:538531 | A | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
43 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.497+1384A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538531 | |||||||
| chr19:538535 | AT | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.497+1400delT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 538535 | ||||||
| chr19:538535 | ATT | A | 8 | a0001c0001t0002g0117 a0001c0001t0004g0051 a0001c0001t0004g0052 others(5): Show |
8 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.497+1399_497+1400d others(4): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 538535 | ||||||
| chr19:538583 | C | T | 1 | a0001c0002t0006g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497+1436C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538583 | |||||||
| chr19:538599 | T | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(6): Show |
20 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.497+1452T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538599 | |||||||
| chr19:538655 | T | C | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+1508T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538655 | |||||||
| chr19:538687 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.497+1540G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538687 | |||||||
| chr19:538731 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0139 |
3 | NA18945.hp1 NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.497+1584C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538731 | |||||||
| chr19:538740 | A | G | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+1593A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538740 | |||||||
| chr19:538776 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.497+1629C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538776 | |||||||
| chr19:538802 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.497+1655C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538802 | |||||||
| chr19:538915 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.497+1768C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538915 | |||||||
| chr19:538930 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(62): Show |
144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.497+1783A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538930 | |||||||
| chr19:538961 | G | A | 2 | a0001c0001t0004g0051 a0001c0001t0004g0057 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.497+1814G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538961 | |||||||
| chr19:538974 | A | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0043 others(7): Show |
14 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+1827A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538974 | |||||||
| chr19:538982 | C | T | 1 | a0001c0002t0003g0071 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.497+1835C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538982 | |||||||
| chr19:538994 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(62): Show |
144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.497+1847C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538994 | |||||||
| chr19:539115 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+1968G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539115 | |||||||
| chr19:539174 | C | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+2027C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539174 | |||||||
| chr19:539203 | T | A | 1 | a0001c0001t0001g0030 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.497+2056T>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539203 | |||||||
| chr19:539222 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+2075G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539222 | |||||||
| chr19:539250 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.498-2089G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539250 | |||||||
| chr19:539266 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.498-2073T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539266 | |||||||
| chr19:539279 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(18): Show |
52 | HG00099.hp1 HG00544.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.498-2060C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539279 | |||||||
| chr19:539323 | C | T | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498-2016C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539323 | |||||||
| chr19:539324 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0003g0105 |
2 | HG02074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.498-2015G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539324 | |||||||
| chr19:539347 | A | AC | 18 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0047 others(15): Show |
23 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-1985dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 539347 | ||||||
| chr19:539412 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG01069.hp1 NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.498-1927C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539412 | |||||||
| chr19:539434 | A | AC | 10 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0002g0146 others(7): Show |
10 | HG01099.hp1 HG01099.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-1898dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 539434 | ||||||
| chr19:539488 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.498-1851C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539488 | |||||||
| chr19:539490 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.498-1849G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539490 | |||||||
| chr19:539593 | C | T | 73 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(70): Show |
152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.498-1746C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539593 | |||||||
| chr19:539678 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.498-1661G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539678 | |||||||
| chr19:539730 | C | G | 5 | a0001c0001t0002g0022 a0001c0001t0002g0127 a0001c0001t0002g0147 others(2): Show |
7 | HG01074.hp2 HG01175.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-1609C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539730 | |||||||
| chr19:539753 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(8): Show |
17 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.498-1586G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539753 | |||||||
| chr19:539812 | C | A | 67 | a0001c0001t0001g0150 a0001c0001t0002g0001 a0001c0001t0002g0002 others(64): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.498-1527C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539812 | |||||||
| chr19:539817 | C | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(63): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.498-1522C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539817 | |||||||
| chr19:539854 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.498-1485G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539854 | |||||||
| chr19:539871 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(18): Show |
52 | HG00099.hp1 HG00544.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.498-1468C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539871 | |||||||
| chr19:539903 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(7): Show |
23 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-1436G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539903 | |||||||
| chr19:539992 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498-1347C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539992 | |||||||
| chr19:539996 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498-1343G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539996 | |||||||
| chr19:540004 | G | GC | 16 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0093 others(13): Show |
25 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-1330dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540004 | ||||||
| chr19:540005 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.498-1334C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540005 | |||||||
| chr19:540011 | G | C | 14 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0002t0003g0005 others(11): Show |
23 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-1328G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540011 | |||||||
| chr19:540011 | G | GGTTTAGA others(328): Show |
1 | a0001c0001t0001g0018 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-1293_498-1292i others(337): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540011 | ||||||
| chr19:540023 | G | A | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-1316G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540023 | |||||||
| chr19:540041 | G | GCCCCCAG others(31): Show |
1 | a0001c0001t0002g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.498-1293_498-1292i others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540041 | ||||||
| chr19:540041 | GC | G | 16 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0002g0010 others(13): Show |
25 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.498-1292delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540041 | ||||||
| chr19:540041 | GCCCCCCA others(32): Show |
G | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498-1292_498-1254d others(41): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540041 | ||||||
| chr19:540042 | C | CCCCCAGG others(67): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-1293_498-1292i others(76): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540042 | ||||||
| chr19:540042 | C | CCCCCAGG others(30): Show |
47 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(44): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.498-1293_498-1292i others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540042 | ||||||
| chr19:540042 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
100 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.498-1297C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540042 | |||||||
| chr19:540048 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.498-1291A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540048 | |||||||
| chr19:540049 | C | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.498-1290C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540049 | |||||||
| chr19:540049 | CGTTTAGA others(410): Show |
C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0106 a0001c0001t0001g0110 others(1): Show |
5 | HG00642.hp1 HG02738.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.498-1253_498-837de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540049 | ||||||
| chr19:540061 | G | A | 49 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0002 others(46): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.498-1278G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540061 | |||||||
| chr19:540067 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0091 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.498-1272C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540067 | |||||||
| chr19:540080 | C | T | 71 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0002g0001 others(68): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.498-1259C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540080 | |||||||
| chr19:540086 | A | G | 9 | a0001c0001t0002g0133 a0001c0001t0002g0137 a0001c0001t0004g0051 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-1253A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540086 | |||||||
| chr19:540087 | G | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(41): Show |
95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.498-1252G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540087 | |||||||
| chr19:540099 | G | A | 13 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0118 others(10): Show |
19 | HG00558.hp1 HG01070.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.498-1240G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540099 | |||||||
| chr19:540106 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0140 |
2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.498-1233G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540106 | |||||||
| chr19:540118 | C | T | 16 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0024 others(13): Show |
25 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.498-1221C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540118 | |||||||
| chr19:540124 | A | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(46): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.498-1215A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540124 | |||||||
| chr19:540124 | ACGTTTAG others(296): Show |
A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 |
6 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-1214_498-912de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540124 | |||||||
| chr19:540125 | C | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(94): Show |
201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.498-1214C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540125 | |||||||
| chr19:540125 | CGTTTAGA others(486): Show |
C | 1 | a0001c0001t0001g0033 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.498-1139_498-647de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540125 | ||||||
| chr19:540147 | G | GTGGCCAG others(68): Show |
3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG02145.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.498-1141_498-1140i others(77): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540147 | ||||||
| chr19:540147 | GTGGCCAG others(636): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.498-1175_498-533de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540147 | ||||||
| chr19:540155 | G | GC | 45 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(42): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.498-1178dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540155 | ||||||
| chr19:540155 | G | GCCCCCCG others(32): Show |
2 | a0001c0001t0002g0119 a0001c0001t0002g0157 |
2 | HG01123.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.498-1178_498-1140d others(41): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540155 | ||||||
| chr19:540155 | GC | G | 13 | a0001c0001t0001g0084 a0001c0002t0003g0005 a0001c0002t0003g0031 others(10): Show |
22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-1178delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540155 | ||||||
| chr19:540162 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(51): Show |
112 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.498-1177G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540162 | |||||||
| chr19:540163 | G | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
91 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.498-1176G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540163 | |||||||
| chr19:540175 | G | A | 13 | a0001c0001t0001g0084 a0001c0002t0003g0005 a0001c0002t0003g0031 others(10): Show |
22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-1164G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540175 | |||||||
| chr19:540181 | C | T | 13 | a0001c0001t0001g0084 a0001c0002t0003g0005 a0001c0002t0003g0031 others(10): Show |
22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-1158C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540181 | |||||||
| chr19:540185 | G | A | 14 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0002t0003g0005 others(11): Show |
23 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-1154G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540185 | |||||||
| chr19:540185 | G | GTGGCCAG others(30): Show |
1 | a0001c0001t0004g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498-1141_498-1140i others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540185 | ||||||
| chr19:540185 | GTGGCCAG others(598): Show |
G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(16): Show |
50 | HG00099.hp1 HG00544.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-1137_498-533de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540185 | ||||||
| chr19:540193 | G | GC | 15 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0024 others(12): Show |
23 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-1140dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540193 | ||||||
| chr19:540194 | CCCCCCGG others(105): Show |
C | 1 | a0001c0001t0002g0010 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.498-1139_498-1028d others(2): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540194 | ||||||
| chr19:540200 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
85 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.498-1139G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540200 | |||||||
| chr19:540201 | G | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
59 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.498-1138G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540201 | |||||||
| chr19:540212 | C | G | 1 | a0001c0003t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.498-1127C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540212 | |||||||
| chr19:540213 | G | A | 3 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0057 |
3 | HG02572.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.498-1126G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540213 | |||||||
| chr19:540219 | C | T | 3 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0057 |
3 | HG02572.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.498-1120C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540219 | |||||||
| chr19:540223 | G | A | 16 | a0001c0001t0001g0084 a0001c0001t0004g0051 a0001c0001t0004g0052 others(13): Show |
25 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-1116G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540223 | |||||||
| chr19:540223 | GTGGCCAG others(523): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498-1102_498-573de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540223 | ||||||
| chr19:540226 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.498-1113G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540226 | |||||||
| chr19:540231 | GC | G | 3 | a0001c0001t0001g0018 a0001c0001t0002g0137 a0001c0001t0003g0105 |
5 | HG00408.hp1 HG02976.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-1102delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540231 | ||||||
| chr19:540232 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-1107C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540232 | |||||||
| chr19:540237 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.498-1102C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540237 | |||||||
| chr19:540237 | CGGGTTTA others(145): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.498-1099_498-948de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540237 | ||||||
| chr19:540238 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(29): Show |
59 | HG00408.hp1 HG00408.hp2 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.498-1101G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540238 | |||||||
| chr19:540238 | GGGTTTAG others(30): Show |
G | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498-1061_498-1025d others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540238 | ||||||
| chr19:540239 | G | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(18): Show |
35 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.498-1100G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540239 | |||||||
| chr19:540251 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-1088G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540251 | |||||||
| chr19:540257 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-1082C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540257 | |||||||
| chr19:540261 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.498-1078G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540261 | |||||||
| chr19:540269 | G | GT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(6): Show |
20 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.498-1070_498-1069i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540269 | |||||||
| chr19:540269 | GCCCCCCG others(411): Show |
G | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-1064_498-647de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540269 | ||||||
| chr19:540274 | C | T | 7 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0024 others(4): Show |
11 | HG00423.hp1 HG01070.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-1065C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540274 | |||||||
| chr19:540275 | C | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
47 | HG00408.hp2 HG01099.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.498-1064C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540275 | |||||||
| chr19:540275 | C | CA | 21 | a0001c0001t0001g0018 a0001c0001t0001g0083 a0001c0001t0001g0084 others(18): Show |
32 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.498-1064_498-1063i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540275 | |||||||
| chr19:540275 | C | CG | 13 | a0001c0001t0001g0093 a0001c0001t0002g0015 a0001c0001t0002g0024 others(10): Show |
15 | HG00558.hp1 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.498-1062dupG | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540275 | C | CGGGTTTA others(32): Show |
1 | a0001c0001t0004g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.498-1062_498-1061i others(41): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540275 | C | CGGTTTAG others(31): Show |
1 | a0001c0001t0001g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-684_498-647dup others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540275 | C | G | 57 | a0001c0001t0001g0090 a0001c0001t0002g0001 a0001c0001t0002g0002 others(54): Show |
131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.498-1064C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540275 | |||||||
| chr19:540275 | CGGTTTAG others(31): Show |
C | 1 | a0001c0001t0001g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.498-684_498-647del others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540275 | CGGTTTAG others(69): Show |
C | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.498-722_498-647del others(76): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540275 | CGGTTTAG others(107): Show |
C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0087 others(2): Show |
7 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-760_498-647del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540275 | CGGTTTAG others(145): Show |
C | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.498-798_498-647del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | ||||||
| chr19:540276 | G | C | 15 | a0001c0001t0001g0084 a0001c0001t0002g0137 a0001c0001t0003g0105 others(12): Show |
24 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.498-1063G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540276 | |||||||
| chr19:540288 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-1051G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540288 | |||||||
| chr19:540298 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(23): Show |
44 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.498-1041G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540298 | |||||||
| chr19:540298 | GTGGCCAG others(485): Show |
G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0028 others(17): Show |
28 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.498-1024_498-533de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540298 | ||||||
| chr19:540306 | GC | G | 61 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(58): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.498-1027delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540306 | ||||||
| chr19:540307 | C | CCCCTGGG others(67): Show |
1 | a0001c0001t0002g0002 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.498-1029_498-1028i others(76): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540307 | ||||||
| chr19:540307 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0043 others(5): Show |
14 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.498-1032C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540307 | |||||||
| chr19:540312 | C | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(47): Show |
120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.498-1027C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540312 | |||||||
| chr19:540313 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0021 others(36): Show |
71 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.498-1026G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540313 | |||||||
| chr19:540314 | G | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(25): Show |
51 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.498-1025G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540314 | |||||||
| chr19:540326 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.498-1013G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540326 | |||||||
| chr19:540326 | G | GGAGGCCG others(181): Show |
1 | a0001c0001t0001g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.498-995_498-994ins others(188): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540326 | ||||||
| chr19:540332 | C | G | 1 | a0001c0002t0003g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.498-1007C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540332 | |||||||
| chr19:540336 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0002g0001 a0001c0001t0002g0002 others(49): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.498-1003G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540336 | |||||||
| chr19:540344 | GC | G | 31 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0002g0010 others(28): Show |
50 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-989delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540344 | ||||||
| chr19:540345 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0090 |
2 | HG01261.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.498-994C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540345 | |||||||
| chr19:540350 | C | T | 15 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0024 others(12): Show |
23 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-989C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540350 | |||||||
| chr19:540350 | CGGGTTTA others(32): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.498-986_498-948del others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540350 | ||||||
| chr19:540351 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(60): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.498-988G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540351 | |||||||
| chr19:540352 | G | C | 52 | a0001c0001t0001g0004 a0001c0001t0002g0001 a0001c0001t0002g0002 others(49): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.498-987G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540352 | |||||||
| chr19:540374 | G | A | 29 | a0001c0001t0001g0084 a0001c0001t0002g0010 a0001c0001t0002g0015 others(26): Show |
45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.498-965G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540374 | |||||||
| chr19:540374 | G | GTGGCCAG others(30): Show |
1 | a0001c0001t0004g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498-952_498-951ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540374 | ||||||
| chr19:540382 | GC | G | 52 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0002 others(49): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.498-951delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540382 | ||||||
| chr19:540382 | GCCCCCCG others(146): Show |
G | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.498-951_498-799del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540382 | ||||||
| chr19:540383 | C | CCCCCAGG others(29): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-952_498-951ins others(36): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540383 | ||||||
| chr19:540383 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0049 others(4): Show |
13 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.498-956C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540383 | |||||||
| chr19:540388 | C | CACGTTTA others(30): Show |
2 | a0001c0001t0002g0015 a0001c0001t0002g0113 |
2 | HG00558.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.498-951_498-950ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540388 | |||||||
| chr19:540388 | C | T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(45): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.498-951C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540388 | |||||||
| chr19:540389 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(37): Show |
69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.498-950G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540389 | |||||||
| chr19:540390 | G | C | 29 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0002g0010 others(26): Show |
45 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-949G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540390 | |||||||
| chr19:540402 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(8): Show |
21 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.498-937G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540402 | |||||||
| chr19:540408 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.498-931C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540408 | |||||||
| chr19:540412 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(52): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.498-927G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540412 | |||||||
| chr19:540412 | G | GTGGCCAG others(30): Show |
1 | a0001c0001t0004g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.498-914_498-913ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540412 | ||||||
| chr19:540419 | GGCCCCCC others(370): Show |
G | 12 | a0001c0001t0001g0084 a0001c0002t0003g0005 a0001c0002t0003g0031 others(9): Show |
21 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-918_498-542del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540419 | ||||||
| chr19:540420 | GC | G | 12 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0024 others(9): Show |
14 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.498-913delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540420 | ||||||
| chr19:540420 | GCCCCCCG others(108): Show |
G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0049 others(3): Show |
11 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-913_498-799del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540420 | ||||||
| chr19:540421 | C | CCCCCAGG others(29): Show |
1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.498-914_498-913ins others(36): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | ||||||
| chr19:540421 | C | CCCCCCAC others(67): Show |
22 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(19): Show |
33 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.498-913_498-912ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | ||||||
| chr19:540421 | C | CCCCCGGG others(29): Show |
7 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0024 others(4): Show |
11 | HG00423.hp1 HG01070.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-914_498-913ins others(36): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | ||||||
| chr19:540421 | C | CCCCTGGG others(104): Show |
2 | a0001c0001t0002g0118 a0001c0001t0007g0132 |
2 | HG01993.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.498-915_498-914ins others(111): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | ||||||
| chr19:540421 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0021 others(14): Show |
29 | HG01099.hp2 HG01123.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.498-918C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540421 | |||||||
| chr19:540426 | C | T | 6 | a0001c0001t0002g0024 a0001c0001t0002g0041 a0001c0001t0002g0115 others(3): Show |
8 | HG00639.hp2 HG01106.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.498-913C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540426 | |||||||
| chr19:540427 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0021 others(52): Show |
116 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.498-912G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540427 | |||||||
| chr19:540428 | G | C | 41 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0002 others(38): Show |
89 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.498-911G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540428 | |||||||
| chr19:540440 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0004g0057 |
2 | HG02148.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.498-899G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540440 | |||||||
| chr19:540443 | GGCCGGGG others(369): Show |
G | 1 | a0001c0002t0003g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.498-894_498-519del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540443 | ||||||
| chr19:540450 | G | A | 8 | a0001c0001t0002g0024 a0001c0001t0002g0041 a0001c0001t0002g0115 others(5): Show |
10 | HG00639.hp2 HG01106.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-889G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540450 | |||||||
| chr19:540458 | GC | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(8): Show |
21 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.498-875delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540458 | ||||||
| chr19:540458 | GCCCCCCG others(70): Show |
G | 1 | a0001c0001t0005g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.498-875_498-799del others(77): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540458 | ||||||
| chr19:540459 | C | CCCCCCAC others(67): Show |
33 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(30): Show |
50 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-875_498-874ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCCAC others(179): Show |
3 | a0001c0001t0002g0115 a0001c0001t0002g0159 a0001c0001t0007g0015 |
3 | HG02273.hp2 HG02735.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.498-875_498-874ins others(186): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCGGG others(141): Show |
1 | a0001c0001t0002g0002 | 2 | NA18951.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCGGG others(141): Show |
1 | a0001c0001t0002g0001 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCGGG others(141): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0135 |
4 | HG00544.hp1 HG00609.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCGGG others(141): Show |
36 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(33): Show |
78 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCGGG others(142): Show |
1 | a0001c0001t0002g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.498-876_498-875ins others(149): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | CCCCCGGG others(67): Show |
1 | a0001c0001t0001g0018 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-876_498-875ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | ||||||
| chr19:540459 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02148.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-880C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540459 | |||||||
| chr19:540464 | C | T | 1 | a0001c0001t0002g0010 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.498-875C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540464 | |||||||
| chr19:540465 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(18): Show |
35 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.498-874G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540465 | |||||||
| chr19:540466 | G | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(10): Show |
23 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-873G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540466 | |||||||
| chr19:540478 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.498-861G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540478 | |||||||
| chr19:540484 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.498-855C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540484 | |||||||
| chr19:540488 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0002g0010 a0001c0001t0002g0144 others(1): Show |
6 | HG00408.hp1 HG03516.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-851G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540488 | |||||||
| chr19:540495 | GGCCCCCC others(294): Show |
G | 1 | a0001c0001t0003g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-842_498-542del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540495 | ||||||
| chr19:540496 | GC | G | 5 | a0001c0001t0001g0004 a0001c0001t0002g0001 a0001c0001t0002g0002 others(2): Show |
5 | HG02148.hp2 HG03669.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-837delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540496 | ||||||
| chr19:540497 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0021 others(16): Show |
25 | HG00642.hp1 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-842C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540497 | |||||||
| chr19:540503 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(75): Show |
169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.498-836G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540503 | |||||||
| chr19:540504 | G | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(69): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.498-835G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540504 | |||||||
| chr19:540504 | G | GGTTTAGA others(31): Show |
3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG02145.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.498-825_498-824ins others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540504 | ||||||
| chr19:540516 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0134 |
3 | HG03669.hp1 NA18944.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.498-823G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540516 | |||||||
| chr19:540522 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.498-817C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540522 | |||||||
| chr19:540526 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0002g0001 a0001c0001t0002g0002 others(1): Show |
6 | HG00408.hp1 HG03669.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-813G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540526 | |||||||
| chr19:540534 | GC | G | 65 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0002g0001 others(62): Show |
141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.498-799delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540534 | ||||||
| chr19:540535 | C | CCCCCCAC others(67): Show |
1 | a0001c0001t0002g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.498-799_498-798ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540535 | ||||||
| chr19:540535 | C | CCCCCGGG others(104): Show |
2 | a0001c0001t0002g0024 a0001c0001t0002g0041 |
4 | HG00639.hp2 HG01106.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-800_498-799ins others(111): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540535 | ||||||
| chr19:540535 | C | T | 1 | a0001c0001t0004g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498-804C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540535 | |||||||
| chr19:540535 | CCCCCCGG others(256): Show |
C | 1 | a0001c0007t0002g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498-798_498-536del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540535 | ||||||
| chr19:540540 | C | T | 1 | a0001c0001t0002g0010 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.498-799C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540540 | |||||||
| chr19:540541 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(20): Show |
44 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.498-798G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540541 | |||||||
| chr19:540542 | G | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0083 |
2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.498-797G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540542 | |||||||
| chr19:540554 | G | A | 63 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(60): Show |
139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.498-785G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540554 | |||||||
| chr19:540564 | G | A | 63 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(60): Show |
139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.498-775G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540564 | |||||||
| chr19:540566 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0002 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.498-773G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540566 | |||||||
| chr19:540572 | GC | G | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(64): Show |
143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.498-761delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540572 | ||||||
| chr19:540573 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0038 others(18): Show |
31 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.498-766C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540573 | |||||||
| chr19:540574 | C | T | 1 | a0001c0003t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.498-765C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540574 | |||||||
| chr19:540579 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0016 others(27): Show |
55 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.498-760G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540579 | |||||||
| chr19:540580 | G | C | 7 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0002 others(4): Show |
7 | HG01261.hp1 HG03669.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-759G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540580 | |||||||
| chr19:540580 | G | GGTTTAGA others(31): Show |
1 | a0001c0001t0004g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.498-749_498-748ins others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540580 | ||||||
| chr19:540580 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.498-759G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540580 | |||||||
| chr19:540591 | C | T | 1 | a0001c0001t0004g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498-748C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540591 | |||||||
| chr19:540598 | C | T | 3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG02145.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.498-741C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540598 | |||||||
| chr19:540602 | G | A | 63 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(60): Show |
139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.498-737G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540602 | |||||||
| chr19:540617 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0016 others(89): Show |
193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.498-722G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540617 | |||||||
| chr19:540618 | G | C | 68 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(65): Show |
147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.498-721G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540618 | |||||||
| chr19:540630 | G | A | 4 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0010 others(1): Show |
4 | HG03669.hp1 NA18944.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-709G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540630 | |||||||
| chr19:540636 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(61): Show |
141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.498-703C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540636 | |||||||
| chr19:540640 | G | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(61): Show |
143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.498-699G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540640 | |||||||
| chr19:540640 | G | GTGGCCAG others(68): Show |
1 | a0001c0001t0004g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498-648_498-647ins others(75): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540640 | ||||||
| chr19:540640 | G | GTGGCCAG others(30): Show |
2 | a0001c0001t0004g0051 a0001c0001t0004g0053 |
2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.498-686_498-685ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540640 | ||||||
| chr19:540648 | GC | G | 65 | a0001c0001t0001g0018 a0001c0001t0002g0001 a0001c0001t0002g0002 others(62): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.498-685delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540648 | ||||||
| chr19:540649 | C | CCCCCAGG others(783): Show |
1 | a0001c0001t0001g0018 | 2 | HG00408.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.498-686_498-685ins others(790): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540649 | ||||||
| chr19:540649 | C | CCCCCGGG others(67): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0144 |
3 | HG03669.hp1 NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.498-686_498-685ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540649 | ||||||
| chr19:540649 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.498-690C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540649 | |||||||
| chr19:540654 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(61): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.498-685C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540654 | |||||||
| chr19:540655 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0016 others(33): Show |
59 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.498-684G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540655 | |||||||
| chr19:540656 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0066 others(1): Show |
8 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-683G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540656 | |||||||
| chr19:540668 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG00408.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.498-671G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540668 | |||||||
| chr19:540678 | G | A | 65 | a0001c0001t0001g0018 a0001c0001t0002g0001 a0001c0001t0002g0002 others(62): Show |
144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.498-661G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540678 | |||||||
| chr19:540678 | G | GTGGCCAG others(784): Show |
1 | a0001c0001t0001g0018 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.498-648_498-647ins others(791): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540678 | ||||||
| chr19:540687 | C | CCCCCGGG others(68): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-648_498-647ins others(75): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540687 | ||||||
| chr19:540694 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(14): Show |
36 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.498-645C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540694 | |||||||
| chr19:540706 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-633G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540706 | |||||||
| chr19:540724 | G | GC | 16 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(13): Show |
26 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.498-610dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540724 | ||||||
| chr19:540730 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(17): Show |
36 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.498-609G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540730 | |||||||
| chr19:540731 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-608G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540731 | |||||||
| chr19:540743 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(91): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.498-596G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540743 | |||||||
| chr19:540749 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(19): Show |
36 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.498-590T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540749 | |||||||
| chr19:540753 | A | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(18): Show |
38 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.498-586A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540753 | |||||||
| chr19:540761 | G | GC | 8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
18 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-573dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540761 | ||||||
| chr19:540761 | G | GCCCCCCA others(108): Show |
1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.498-573_498-572ins others(115): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540761 | ||||||
| chr19:540767 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(13): Show |
29 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.498-572G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540767 | |||||||
| chr19:540768 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(5): Show |
19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-571G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540768 | |||||||
| chr19:540768 | G | GGTTTAGA others(145): Show |
1 | a0001c0001t0001g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.498-554_498-553ins others(152): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540768 | ||||||
| chr19:540778 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.498-561C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540778 | |||||||
| chr19:540780 | A | G | 68 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0002g0001 others(65): Show |
155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.498-559A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540780 | |||||||
| chr19:540786 | T | C | 73 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0002g0001 others(70): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.498-553T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540786 | |||||||
| chr19:540790 | A | G | 72 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0002g0001 others(69): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.498-549A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540790 | |||||||
| chr19:540790 | ATGGCCAG others(30): Show |
A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0066 others(1): Show |
8 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-535_498-499del others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540790 | ||||||
| chr19:540798 | G | T | 13 | a0001c0001t0001g0084 a0001c0001t0003g0105 a0001c0002t0003g0005 others(10): Show |
22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-541G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540798 | |||||||
| chr19:540804 | C | A | 15 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0003g0105 others(12): Show |
26 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.498-535C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | |||||||
| chr19:540804 | C | CA | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0027 others(77): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.498-535_498-534ins others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | |||||||
| chr19:540804 | C | CACGTTTA others(180): Show |
1 | a0001c0001t0002g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.498-535_498-534ins others(187): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | |||||||
| chr19:540804 | C | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(38): Show |
80 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.498-535C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | |||||||
| chr19:540805 | G | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0027 others(86): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.498-534G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540805 | |||||||
| chr19:540817 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(38): Show |
80 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.498-522G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540817 | |||||||
| chr19:540817 | G | GGAGGCCG others(184): Show |
1 | a0001c0001t0004g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.498-499_498-498ins others(191): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540817 | ||||||
| chr19:540817 | G | GGAGGCCG others(33): Show |
6 | a0001c0001t0004g0051 a0001c0001t0004g0053 a0001c0001t0004g0054 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-500_498-499ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540817 | ||||||
| chr19:540823 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(37): Show |
78 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.498-516C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540823 | |||||||
| chr19:540827 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(37): Show |
78 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.498-512G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540827 | |||||||
| chr19:540881 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.498-458G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540881 | |||||||
| chr19:540881 | G | GT | 7 | a0001c0001t0001g0064 a0001c0001t0001g0091 a0001c0001t0001g0110 others(4): Show |
7 | HG00738.hp1 HG02135.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-453dupT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540881 | ||||||
| chr19:540917 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG02486.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.498-422G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540917 | |||||||
| chr19:541095 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
102 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.498-244C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541095 | |||||||
| chr19:541124 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
8 | HG01192.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.498-215C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541124 | |||||||
| chr19:541133 | G | A | 14 | a0001c0001t0001g0084 a0001c0001t0003g0105 a0001c0002t0003g0005 others(11): Show |
23 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-206G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541133 | |||||||
| chr19:541155 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.498-184C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541155 | |||||||
| chr19:541217 | G | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0038 others(15): Show |
23 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-122G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541217 | |||||||
| chr19:541242 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(8): Show |
25 | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-97T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541242 | |||||||
| chr19:541260 | T | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
54 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(51): Show |
intron_variant | MODIFIER | c.498-79T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541260 | |||||||
| chr19:541262 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.498-77G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541262 |