Item | Value |
---|---|
geneid | 894 |
ensemblid | ENSG00000118971.9 |
hgncid | 1583 |
symbol | CCND2 |
name | cyclin D2 |
refseq_nuc | NM_001759.4 |
refseq_prot | NP_001750.1 |
ensembl_nuc | ENST00000261254.8 |
ensembl_prot | ENSP00000261254.3 |
mane_status | MANE Select |
chr | chr12 |
start | 4273762 |
end | 4305353 |
strand | + |
ver | v1.2 |
region | chr12:4273762-4305353 |
region5000 | chr12:4268762-4310353 |
regionname0 | CCND2_chr12_4273762_4305353 |
regionname5000 | CCND2_chr12_4268762_4310353 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 867 | 361 | 77 | 68 | 169 | 7 | 39 | CCND2_chr12_4268762_4310353 | CCND2 | ATGGA others(862): Show |
chr12 | 4268762 | 4310353 | ||
a0001c0002 | 0/1 | 867 | 99 | 23 | 16 | 45 | 5 | 9 | CCND2_chr12_4268762_4310353 | CCND2 | ATGGA others(862): Show |
chr12 | 4268762 | 4310353 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6491 | 37 | 2 | 3 | 28 | 1 | 3 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0002 | 0/0 | 6492 | 35 | 2 | 9 | 23 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0003 | 0/0 | 6492 | 33 | 0 | 14 | 12 | 2 | 5 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0004 | 0/0 | 6491 | 11 | 0 | 3 | 5 | 1 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0005 | 0/0 | 6492 | 10 | 0 | 6 | 2 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0006 | 0/0 | 6491 | 21 | 9 | 1 | 9 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0007 | 0/0 | 6495 | 3 | 0 | 0 | 3 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6490): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0008 | 0/0 | 6492 | 18 | 3 | 10 | 5 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0009 | 0/0 | 6492 | 14 | 2 | 0 | 7 | 0 | 5 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0010 | 0/0 | 6492 | 9 | 3 | 1 | 2 | 1 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0011 | 0/0 | 6494 | 15 | 0 | 0 | 15 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0012 | 0/0 | 6491 | 9 | 2 | 0 | 5 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0013 | 0/0 | 6493 | 7 | 1 | 0 | 6 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0014 | 0/0 | 6492 | 7 | 0 | 1 | 5 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0015 | 0/0 | 6492 | 7 | 1 | 0 | 6 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0016 | 0/0 | 6493 | 5 | 1 | 2 | 0 | 1 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0017 | 0/0 | 6490 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6485): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0018 | 0/0 | 6494 | 3 | 0 | 0 | 3 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0019 | 0/0 | 6492 | 5 | 0 | 0 | 4 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0020 | 0/0 | 6491 | 5 | 5 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0021 | 0/0 | 6493 | 5 | 2 | 2 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0022 | 0/0 | 6495 | 3 | 0 | 1 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6490): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0023 | 0/0 | 6494 | 4 | 4 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0024 | 0/0 | 6489 | 4 | 3 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6484): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0025 | 0/0 | 6492 | 4 | 0 | 2 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0026 | 0/0 | 6493 | 2 | 1 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0027 | 0/0 | 6492 | 3 | 0 | 0 | 3 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0028 | 0/0 | 6493 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0029 | 1/0 | 6493 | 3 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0030 | 0/0 | 6492 | 3 | 0 | 0 | 3 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0031 | 0/0 | 6493 | 3 | 3 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0032 | 0/0 | 6492 | 2 | 0 | 0 | 0 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0033 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0034 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0036 | 0/0 | 6493 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0037 | 0/0 | 6491 | 2 | 0 | 0 | 0 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0038 | 0/0 | 6493 | 2 | 0 | 0 | 1 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0039 | 0/0 | 6492 | 2 | 1 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0040 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0041 | 0/0 | 6493 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0042 | 0/0 | 6494 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0043 | 0/0 | 6491 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0044 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0045 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0046 | 0/0 | 6492 | 2 | 0 | 1 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0047 | 0/0 | 6492 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0048 | 0/0 | 6495 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6490): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0049 | 0/0 | 6493 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0050 | 0/0 | 6492 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0053 | 0/0 | 6491 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0054 | 0/0 | 6490 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6485): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0058 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0059 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0060 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0061 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0062 | 0/0 | 6492 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0063 | 0/0 | 6492 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0064 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0066 | 0/0 | 6492 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0067 | 0/0 | 6490 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6485): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0068 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0069 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0070 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0071 | 0/0 | 6492 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0072 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0073 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0074 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0075 | 0/0 | 6492 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0076 | 0/0 | 6481 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6476): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0077 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0078 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0079 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0080 | 0/0 | 6492 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0081 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0082 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0083 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0084 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0085 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0086 | 0/0 | 6494 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0087 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0088 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0089 | 0/0 | 6494 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0091 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0092 | 0/0 | 6497 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6492): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0093 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0094 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0001t0095 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0001 | 0/0 | 6491 | 5 | 0 | 0 | 4 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0002 | 0/0 | 6492 | 4 | 1 | 3 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0003 | 0/0 | 6492 | 3 | 0 | 1 | 1 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0004 | 0/0 | 6491 | 19 | 2 | 3 | 12 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0005 | 0/1 | 6492 | 12 | 3 | 2 | 3 | 0 | 3 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0007 | 0/0 | 6495 | 16 | 0 | 2 | 13 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6490): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0008 | 0/0 | 6492 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0009 | 0/0 | 6492 | 3 | 1 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0010 | 0/0 | 6492 | 6 | 1 | 2 | 0 | 3 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0012 | 0/0 | 6491 | 4 | 2 | 0 | 0 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0016 | 0/0 | 6493 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0017 | 0/0 | 6490 | 3 | 3 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6485): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0018 | 0/0 | 6494 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0022 | 0/0 | 6495 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6490): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0026 | 0/0 | 6493 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0028 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0033 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0034 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0035 | 0/0 | 6493 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0040 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0044 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0045 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6487): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0051 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0052 | 0/0 | 6489 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6484): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0055 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0056 | 0/0 | 6490 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6485): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0057 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6488): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0065 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0090 | 0/0 | 6494 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6489): Show |
chr12 | 4268762 | 4310353 |
a0001c0002t0096 | 0/0 | 6491 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | AGAGC others(6486): Show |
chr12 | 4268762 | 4310353 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0006g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0009g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0010g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0011g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0012g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0013g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0013g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0014g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0015g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0016g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0016g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0016g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0017g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0017g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0018g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0018g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0018g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0019g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0019g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0019g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0019g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0020g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0020g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0021g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0021g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0021g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0021g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0022g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0022g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0023g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0023g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0023g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0024g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0024g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0024g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0025g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0025g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0025g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0025g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0026g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0026g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0027g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0027g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0027g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0028g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0028g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0029g0019 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0029g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0030g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0030g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0030g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0031g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0031g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0031g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0032g0059 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0033g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0034g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0036g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0037g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0037g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0038g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0038g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0039g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0039g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0040g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0041g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0042g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0043g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0043g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0044g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0045g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0046g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0046g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0047g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0047g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0048g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0048g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0049g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0050g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0050g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0053g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0054g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0058g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0059g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0060g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0061g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0062g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0063g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0064g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0066g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0067g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0068g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0069g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0070g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0071g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0072g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0073g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0074g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0075g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0076g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0077g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0078g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0079g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0080g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0081g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0082g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0083g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0084g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0085g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0086g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0087g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0088g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0089g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0091g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0092g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0093g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0094g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0001t0095g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0007g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0010g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0010g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0010g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0010g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0012g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0012g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0012g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0016g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0017g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0017g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0018g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0018g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0022g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0026g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0026g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0028g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0033g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0034g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0035g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0040g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0044g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0045g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0051g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0052g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0055g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0056g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0057g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0065g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0090g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
a0001c0002t0096g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0010 | g0206 | EUR | GBR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00099 | hp2 | a0001 | c0002 | t0010 | g0215 | EUR | GBR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0354 | EUR | GBR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | GBR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00323 | hp1 | a0001 | c0001 | t0066 | g0042 | EUR | FIN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0287 | EUR | FIN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00408 | hp2 | a0001 | c0001 | t0079 | g0188 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00423 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00423 | hp2 | a0001 | c0001 | t0011 | g0197 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00438 | hp2 | a0001 | c0001 | t0027 | g0277 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00544 | hp1 | a0001 | c0001 | t0015 | g0142 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00544 | hp2 | a0001 | c0001 | t0087 | g0046 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0299 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00597 | hp1 | a0001 | c0001 | t0091 | g0333 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00597 | hp2 | a0001 | c0001 | t0025 | g0347 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00609 | hp2 | a0001 | c0001 | t0012 | g0285 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00621 | hp1 | a0001 | c0001 | t0030 | g0182 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0092 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0340 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0259 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0238 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00673 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00673 | hp2 | a0001 | c0001 | t0018 | g0242 | EAS | CHS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00733 | hp1 | a0001 | c0001 | t0025 | g0216 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00735 | hp1 | a0001 | c0001 | t0089 | g0009 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00735 | hp2 | a0001 | c0001 | t0053 | g0038 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0351 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG00741 | hp2 | a0001 | c0001 | t0021 | g0154 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01069 | hp1 | a0001 | c0001 | t0036 | g0052 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01069 | hp2 | a0001 | c0002 | t0056 | g0369 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01070 | hp1 | a0001 | c0002 | t0004 | g0091 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01071 | hp1 | a0001 | c0001 | t0036 | g0052 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01071 | hp2 | a0001 | c0001 | t0016 | g0043 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0367 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01099 | hp1 | a0001 | c0001 | t0014 | g0322 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01099 | hp2 | a0001 | c0001 | t0046 | g0258 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01167 | hp1 | a0001 | c0001 | t0049 | g0056 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01168 | hp2 | a0001 | c0002 | t0010 | g0027 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01169 | hp1 | a0001 | c0002 | t0010 | g0027 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01169 | hp2 | a0001 | c0001 | t0049 | g0056 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0318 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01192 | hp2 | a0001 | c0001 | t0026 | g0372 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01243 | hp1 | a0001 | c0002 | t0016 | g0009 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0159 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01256 | hp1 | a0001 | c0001 | t0016 | g0023 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0308 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0244 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01261 | hp1 | a0001 | c0001 | t0008 | g0291 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0294 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01358 | hp1 | a0001 | c0001 | t0086 | g0336 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01358 | hp2 | a0001 | c0001 | t0024 | g0175 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0105 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01361 | hp2 | a0001 | c0001 | t0080 | g0112 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01433 | hp1 | a0001 | c0001 | t0076 | g0257 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01433 | hp2 | a0001 | c0002 | t0005 | g0041 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0209 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0325 | EUR | IBS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01516 | hp2 | a0001 | c0002 | t0010 | g0042 | EUR | IBS | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01884 | hp1 | a0001 | c0001 | t0050 | g0083 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01891 | hp1 | a0001 | c0001 | t0043 | g0079 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01928 | hp1 | a0001 | c0002 | t0007 | g0001 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01928 | hp2 | a0001 | c0001 | t0022 | g0001 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01934 | hp1 | a0001 | c0001 | t0075 | g0004 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01934 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0302 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01952 | hp1 | a0001 | c0002 | t0007 | g0001 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0298 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01978 | hp2 | a0001 | c0001 | t0021 | g0343 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01981 | hp1 | a0001 | c0001 | t0025 | g0030 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01993 | hp1 | a0001 | c0002 | t0090 | g0211 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01993 | hp2 | a0001 | c0001 | t0008 | g0356 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02015 | hp2 | a0001 | c0001 | t0015 | g0220 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0198 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02027 | hp2 | a0001 | c0002 | t0004 | g0031 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02040 | hp1 | a0001 | c0001 | t0015 | g0324 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02040 | hp2 | a0001 | c0001 | t0015 | g0315 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02055 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02055 | hp2 | a0001 | c0001 | t0021 | g0174 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0366 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02074 | hp2 | a0001 | c0001 | t0011 | g0034 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02080 | hp1 | a0001 | c0001 | t0047 | g0144 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02083 | hp1 | a0001 | c0001 | t0045 | g0067 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02132 | hp1 | a0001 | c0001 | t0018 | g0093 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02132 | hp2 | a0001 | c0001 | t0027 | g0262 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02135 | hp2 | a0001 | c0001 | t0030 | g0301 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02145 | hp1 | a0001 | c0001 | t0072 | g0021 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02145 | hp2 | a0001 | c0001 | t0059 | g0066 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0213 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CDX | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02155 | hp2 | a0001 | c0001 | t0012 | g0243 | EAS | CDX | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | CDX | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CDX | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02257 | hp1 | a0001 | c0001 | t0063 | g0014 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02257 | hp2 | a0001 | c0002 | t0008 | g0207 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02258 | hp1 | a0001 | c0002 | t0035 | g0026 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02258 | hp2 | a0001 | c0001 | t0023 | g0073 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02280 | hp1 | a0001 | c0001 | t0058 | g0214 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02280 | hp2 | a0001 | c0002 | t0026 | g0217 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02451 | hp1 | a0001 | c0001 | t0070 | g0076 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02451 | hp2 | a0001 | c0001 | t0071 | g0021 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02523 | hp2 | a0001 | c0001 | t0082 | g0039 | EAS | KHV | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02572 | hp1 | a0001 | c0001 | t0068 | g0292 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02572 | hp2 | a0001 | c0001 | t0040 | g0140 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02602 | hp2 | a0001 | c0001 | t0046 | g0050 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02615 | hp1 | a0001 | c0001 | t0024 | g0016 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02615 | hp2 | a0001 | c0001 | t0042 | g0017 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02622 | hp1 | a0001 | c0002 | t0017 | g0116 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02622 | hp2 | a0001 | c0001 | t0048 | g0172 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02630 | hp1 | a0001 | c0002 | t0026 | g0094 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02647 | hp1 | a0001 | c0001 | t0050 | g0373 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0072 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0274 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0250 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02698 | hp1 | a0001 | c0001 | t0016 | g0004 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0176 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02717 | hp2 | a0001 | c0002 | t0012 | g0101 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02723 | hp1 | a0001 | c0001 | t0023 | g0018 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02723 | hp2 | a0001 | c0001 | t0020 | g0005 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02738 | hp1 | a0001 | c0002 | t0012 | g0346 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02738 | hp2 | a0001 | c0001 | t0044 | g0353 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02809 | hp1 | a0001 | c0001 | t0023 | g0018 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0331 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02818 | hp2 | a0001 | c0002 | t0028 | g0119 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02886 | hp1 | a0001 | c0002 | t0004 | g0121 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0075 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02895 | hp1 | a0001 | c0002 | t0017 | g0025 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02895 | hp2 | a0001 | c0001 | t0069 | g0078 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02896 | hp1 | a0001 | c0002 | t0005 | g0022 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02897 | hp1 | a0001 | c0002 | t0005 | g0022 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02897 | hp2 | a0001 | c0002 | t0017 | g0025 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02965 | hp1 | a0001 | c0001 | t0084 | g0310 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02970 | hp1 | a0001 | c0002 | t0065 | g0118 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02970 | hp2 | a0001 | c0001 | t0074 | g0016 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02976 | hp1 | a0001 | c0002 | t0009 | g0099 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0097 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0192 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03017 | hp2 | a0001 | c0001 | t0012 | g0060 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03041 | hp1 | a0001 | c0001 | t0017 | g0249 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0131 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03098 | hp1 | a0001 | c0001 | t0043 | g0312 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03130 | hp2 | a0001 | c0001 | t0024 | g0016 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03139 | hp2 | a0001 | c0001 | t0041 | g0014 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03195 | hp1 | a0001 | c0001 | t0017 | g0071 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03195 | hp2 | a0001 | c0001 | t0028 | g0307 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03209 | hp1 | a0001 | c0002 | t0040 | g0117 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03209 | hp2 | a0001 | c0001 | t0020 | g0357 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03225 | hp1 | a0001 | c0001 | t0048 | g0338 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03225 | hp2 | a0001 | c0001 | t0028 | g0137 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03239 | hp1 | a0001 | c0001 | t0010 | g0265 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03239 | hp2 | a0001 | c0001 | t0009 | g0266 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03453 | hp1 | a0001 | c0001 | t0020 | g0005 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03453 | hp2 | a0001 | c0001 | t0021 | g0330 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03486 | hp1 | a0001 | c0001 | t0020 | g0005 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03490 | hp2 | a0001 | c0001 | t0032 | g0059 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03491 | hp2 | a0001 | c0001 | t0009 | g0248 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03492 | hp1 | a0001 | c0001 | t0033 | g0054 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03492 | hp2 | a0001 | c0001 | t0032 | g0059 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03516 | hp1 | a0001 | c0001 | t0034 | g0068 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0081 | AFR | ESN | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03540 | hp1 | a0001 | c0002 | t0052 | g0114 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03540 | hp2 | a0001 | c0001 | t0067 | g0082 | AFR | GWD | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03579 | hp2 | a0001 | c0001 | t0024 | g0358 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03654 | hp1 | a0001 | c0002 | t0012 | g0178 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03654 | hp2 | a0001 | c0001 | t0037 | g0278 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03669 | hp2 | a0001 | c0001 | t0010 | g0352 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03688 | hp1 | a0001 | c0001 | t0014 | g0011 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03688 | hp2 | a0001 | c0001 | t0019 | g0306 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03704 | hp1 | a0001 | c0001 | t0038 | g0365 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0256 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03710 | hp1 | a0001 | c0002 | t0096 | g0129 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0335 | SAS | PJL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03834 | hp1 | a0001 | c0001 | t0009 | g0254 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03927 | hp2 | a0001 | c0002 | t0007 | g0133 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0050 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0247 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04115 | hp1 | a0001 | c0002 | t0005 | g0041 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0370 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04184 | hp1 | a0001 | c0001 | t0062 | g0064 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | BEB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04199 | hp1 | a0001 | c0001 | t0009 | g0269 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04199 | hp2 | a0001 | c0001 | t0039 | g0271 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04204 | hp1 | a0001 | c0002 | t0005 | g0205 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04204 | hp2 | a0001 | c0001 | t0012 | g0168 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04228 | hp1 | a0001 | c0001 | t0021 | g0295 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG04228 | hp2 | a0001 | c0002 | t0005 | g0134 | SAS | STU | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18522 | hp1 | a0001 | c0001 | t0020 | g0005 | AFR | YRI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | YRI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18612 | hp1 | a0001 | c0001 | t0014 | g0185 | EAS | CHB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0334 | EAS | CHB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | YRI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18906 | hp2 | a0001 | c0001 | t0060 | g0061 | AFR | YRI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18939 | hp2 | a0001 | c0001 | t0019 | g0288 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18941 | hp2 | a0001 | c0002 | t0009 | g0128 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18942 | hp1 | a0001 | c0001 | t0015 | g0221 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18943 | hp1 | a0001 | c0001 | t0094 | g0045 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18943 | hp2 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0055 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18946 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18946 | hp2 | a0001 | c0001 | t0010 | g0201 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18947 | hp1 | a0001 | c0001 | t0011 | g0169 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18948 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18949 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18950 | hp2 | a0001 | c0001 | t0095 | g0045 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18951 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18952 | hp2 | a0001 | c0001 | t0019 | g0309 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18953 | hp2 | a0001 | c0001 | t0047 | g0360 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18954 | hp2 | a0001 | c0001 | t0008 | g0280 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18957 | hp1 | a0001 | c0002 | t0051 | g0069 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18957 | hp2 | a0001 | c0002 | t0022 | g0020 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18960 | hp1 | a0001 | c0002 | t0004 | g0122 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18960 | hp2 | a0001 | c0001 | t0022 | g0296 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18961 | hp1 | a0001 | c0002 | t0004 | g0339 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18962 | hp1 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18963 | hp1 | a0001 | c0001 | t0009 | g0286 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18963 | hp2 | a0001 | c0002 | t0045 | g0015 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18965 | hp1 | a0001 | c0001 | t0027 | g0264 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18965 | hp2 | a0001 | c0001 | t0018 | g0313 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0314 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18969 | hp1 | a0001 | c0002 | t0007 | g0001 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18970 | hp2 | a0001 | c0002 | t0007 | g0125 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18973 | hp1 | a0001 | c0001 | t0012 | g0273 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18974 | hp1 | a0001 | c0002 | t0007 | g0013 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18974 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18975 | hp1 | a0001 | c0001 | t0077 | g0235 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18975 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18977 | hp1 | a0001 | c0001 | t0038 | g0203 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18977 | hp2 | a0001 | c0001 | t0012 | g0320 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18978 | hp2 | a0001 | c0001 | t0011 | g0364 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18980 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18980 | hp2 | a0001 | c0002 | t0007 | g0135 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18981 | hp1 | a0001 | c0001 | t0083 | g0344 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18981 | hp2 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18982 | hp1 | a0001 | c0001 | t0081 | g0006 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18983 | hp1 | a0001 | c0002 | t0004 | g0089 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18985 | hp2 | a0001 | c0001 | t0007 | g0311 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18989 | hp1 | a0001 | c0001 | t0012 | g0270 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18990 | hp1 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18990 | hp2 | a0001 | c0001 | t0073 | g0231 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18991 | hp1 | a0001 | c0001 | t0006 | g0345 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18991 | hp2 | a0001 | c0002 | t0044 | g0321 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18994 | hp2 | a0001 | c0002 | t0007 | g0013 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18995 | hp2 | a0001 | c0001 | t0009 | g0283 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18997 | hp2 | a0001 | c0002 | t0022 | g0020 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18998 | hp1 | a0001 | c0001 | t0088 | g0164 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0120 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18999 | hp2 | a0001 | c0001 | t0092 | g0297 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19001 | hp1 | a0001 | c0001 | t0010 | g0199 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19001 | hp2 | a0001 | c0001 | t0009 | g0279 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19002 | hp1 | a0001 | c0002 | t0007 | g0219 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0055 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19003 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19003 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0053 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19005 | hp2 | a0001 | c0001 | t0078 | g0186 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19007 | hp1 | a0001 | c0001 | t0011 | g0167 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19007 | hp2 | a0001 | c0002 | t0055 | g0124 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19009 | hp2 | a0001 | c0002 | t0018 | g0126 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0261 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19011 | hp1 | a0001 | c0001 | t0011 | g0236 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19011 | hp2 | a0001 | c0002 | t0005 | g0088 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19012 | hp2 | a0001 | c0002 | t0007 | g0349 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19030 | hp1 | a0001 | c0001 | t0039 | g0138 | AFR | LWK | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19030 | hp2 | a0001 | c0001 | t0042 | g0017 | AFR | LWK | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19043 | hp1 | a0001 | c0001 | t0029 | g0019 | AFR | LWK | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19043 | hp2 | a0001 | c0001 | t0026 | g0371 | AFR | LWK | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19054 | hp1 | a0001 | c0001 | t0025 | g0227 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19054 | hp2 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19055 | hp1 | a0001 | c0001 | t0061 | g0276 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19055 | hp2 | a0001 | c0002 | t0007 | g0049 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19057 | hp1 | a0001 | c0001 | t0030 | g0040 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19057 | hp2 | a0001 | c0001 | t0014 | g0226 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19058 | hp1 | a0001 | c0002 | t0004 | g0127 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19059 | hp1 | a0001 | c0002 | t0007 | g0013 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19059 | hp2 | a0001 | c0001 | t0013 | g0348 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0290 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19064 | hp2 | a0001 | c0001 | t0022 | g0150 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19065 | hp1 | a0001 | c0001 | t0014 | g0189 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19066 | hp1 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19066 | hp2 | a0001 | c0001 | t0019 | g0289 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19068 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19068 | hp2 | a0001 | c0002 | t0005 | g0136 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19070 | hp1 | a0001 | c0002 | t0007 | g0001 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19079 | hp1 | a0001 | c0002 | t0007 | g0049 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19080 | hp1 | a0001 | c0002 | t0018 | g0123 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19080 | hp2 | a0001 | c0001 | t0011 | g0316 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19081 | hp1 | a0001 | c0001 | t0054 | g0267 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19081 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19082 | hp1 | a0001 | c0002 | t0009 | g0130 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19082 | hp2 | a0001 | c0001 | t0011 | g0034 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19083 | hp1 | a0001 | c0002 | t0057 | g0132 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19083 | hp2 | a0001 | c0002 | t0033 | g0028 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19084 | hp1 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19085 | hp1 | a0001 | c0002 | t0007 | g0253 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19087 | hp1 | a0001 | c0001 | t0015 | g0224 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19087 | hp2 | a0001 | c0002 | t0004 | g0051 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19088 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19090 | hp2 | a0001 | c0002 | t0007 | g0252 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19091 | hp1 | a0001 | c0001 | t0011 | g0317 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0057 | AFR | YRI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA19240 | hp2 | a0001 | c0001 | t0031 | g0086 | AFR | YRI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20129 | hp1 | a0001 | c0002 | t0005 | g0100 | AFR | ASW | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ASW | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | TSI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0102 | EUR | TSI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20805 | hp1 | a0001 | c0001 | t0016 | g0004 | EUR | TSI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20805 | hp2 | a0001 | c0001 | t0010 | g0103 | EUR | TSI | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20905 | hp1 | a0001 | c0001 | t0037 | g0145 | SAS | GIH | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20905 | hp2 | a0001 | c0001 | t0064 | g0284 | SAS | GIH | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0337 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | CLM | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02109 | hp1 | a0001 | c0001 | t0031 | g0098 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02109 | hp2 | a0001 | c0001 | t0029 | g0080 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02486 | hp1 | a0001 | c0001 | t0093 | g0173 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0012 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02559 | hp1 | a0001 | c0001 | t0031 | g0096 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG02559 | hp2 | a0001 | c0002 | t0010 | g0326 | AFR | ACB | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03471 | hp1 | a0001 | c0002 | t0035 | g0026 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG03471 | hp2 | a0001 | c0001 | t0085 | g0108 | AFR | MSL | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG06807 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | USA | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
HG06807 | hp2 | a0001 | c0002 | t0034 | g0115 | AFR | USA | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18955 | hp1 | a0001 | c0001 | t0014 | g0184 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | USA | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA20300 | hp2 | a0001 | c0001 | t0041 | g0014 | AFR | USA | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | LWK | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
NA21309 | hp2 | a0001 | c0002 | t0012 | g0293 | AFR | LWK | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
homoSapiens | chm13v2 | a0001 | c0002 | t0005 | g0208 | REF | REF | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
homoSapiens | grch38p0 | a0001 | c0001 | t0029 | g0019 | REF | REF | CCND2_chr12_4268762_4310353 | CCND2 | chr12 | 4268762 | 4310353 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4278918 | C | G | 1 | a0001c0002 | 98 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(95): Show |
splice_region_variant&synonymous_variant | LOW | c.570C>G | p.Thr190Thr | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/5 | 849/6493 | 570/870 | 190/289 | chr12 | 4278918 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4273870 | C | T | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
272 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(269): Show |
5_prime_UTR_variant | MODIFIER | c.-171C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/5 | 171 | chr12 | 4273870 | ||||||
chr12:4273992 | T | C | 110 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(107): Show |
446 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(443): Show |
5_prime_UTR_variant | MODIFIER | c.-49T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/5 | 49 | chr12 | 4273992 | ||||||
chr12:4300040 | C | T | 1 | a0001c0001t0050 | 2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*31C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 31 | chr12 | 4300040 | ||||||
chr12:4300041 | G | A | 3 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 |
3 | HG02145.hp1 HG02451.hp2 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*32G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 32 | chr12 | 4300041 | ||||||
chr12:4300045 | A | C | 1 | a0001c0002t0096 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 36 | chr12 | 4300045 | ||||||
chr12:4300174 | C | T | 1 | a0001c0001t0049 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*165C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 165 | chr12 | 4300174 | ||||||
chr12:4300714 | T | G | 1 | a0001c0002t0051 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 705 | chr12 | 4300714 | ||||||
chr12:4300778 | A | G | 3 | a0001c0001t0066 a0001c0001t0094 a0001c0001t0095 |
3 | HG00323.hp1 NA18943.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*769A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 769 | chr12 | 4300778 | ||||||
chr12:4301353 | G | GT | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0025 others(22): Show |
104 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1357dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1358 | INFO_REALIGN_3_PRIME | chr12 | 4301353 | |||||
chr12:4301353 | G | GTT | 24 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0015 others(21): Show |
70 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1356_*1357dupTT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1358 | INFO_REALIGN_3_PRIME | chr12 | 4301353 | |||||
chr12:4301353 | GT | G | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(47): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*1357delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1357 | INFO_REALIGN_3_PRIME | chr12 | 4301353 | |||||
chr12:4301472 | C | CT | 6 | a0001c0001t0023 a0001c0001t0042 a0001c0001t0047 others(3): Show |
12 | HG02080.hp1 HG02258.hp2 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1479dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1480 | INFO_REALIGN_3_PRIME | chr12 | 4301472 | |||||
chr12:4301615 | G | GT | 10 | a0001c0001t0023 a0001c0001t0026 a0001c0001t0028 others(7): Show |
17 | HG01192.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1607dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1608 | INFO_REALIGN_3_PRIME | chr12 | 4301615 | |||||
chr12:4301663 | A | C | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1654A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1654 | chr12 | 4301663 | ||||||
chr12:4301684 | G | GT | 13 | a0001c0001t0016 a0001c0001t0021 a0001c0001t0030 others(10): Show |
23 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1690dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1691 | INFO_REALIGN_3_PRIME | chr12 | 4301684 | |||||
chr12:4301684 | GT | G | 37 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 others(34): Show |
131 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1690delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1690 | INFO_REALIGN_3_PRIME | chr12 | 4301684 | |||||
chr12:4301912 | G | GGTT | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1907_*1909dupGTT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1910 | INFO_REALIGN_3_PRIME | chr12 | 4301912 | |||||
chr12:4301944 | G | GT | 8 | a0001c0001t0040 a0001c0001t0044 a0001c0001t0048 others(5): Show |
9 | HG02280.hp1 HG02523.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1947dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1948 | INFO_REALIGN_3_PRIME | chr12 | 4301944 | |||||
chr12:4301944 | GT | G | 3 | a0001c0001t0024 a0001c0001t0074 a0001c0002t0052 |
6 | HG01358.hp2 HG02615.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1947delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 1947 | INFO_REALIGN_3_PRIME | chr12 | 4301944 | |||||
chr12:4302391 | C | T | 8 | a0001c0001t0017 a0001c0001t0024 a0001c0001t0041 others(5): Show |
15 | HG01358.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2382C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2382 | chr12 | 4302391 | ||||||
chr12:4302473 | C | T | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 others(31): Show |
126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2464C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2464 | chr12 | 4302473 | ||||||
chr12:4302517 | T | C | 16 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0013 others(13): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2508T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2508 | chr12 | 4302517 | ||||||
chr12:4302537 | G | A | 2 | a0001c0001t0041 a0001c0001t0063 |
3 | HG02257.hp1 HG03139.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2528G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2528 | chr12 | 4302537 | ||||||
chr12:4302638 | G | A | 93 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(90): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*2629G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2629 | chr12 | 4302638 | ||||||
chr12:4302685 | T | C | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2676T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2676 | chr12 | 4302685 | ||||||
chr12:4302708 | A | G | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2699A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2699 | chr12 | 4302708 | ||||||
chr12:4302720 | T | C | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2711T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2711 | chr12 | 4302720 | ||||||
chr12:4302721 | T | G | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2712T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2712 | chr12 | 4302721 | ||||||
chr12:4302935 | GC | G | 3 | a0001c0001t0011 a0001c0001t0018 a0001c0002t0018 |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2928delC | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2928 | INFO_REALIGN_3_PRIME | chr12 | 4302935 | |||||
chr12:4302993 | C | T | 4 | a0001c0001t0032 a0001c0001t0069 a0001c0001t0085 others(1): Show |
6 | HG02258.hp1 HG02895.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 2984 | chr12 | 4302993 | ||||||
chr12:4303009 | C | A | 1 | a0001c0001t0077 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3000C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3000 | chr12 | 4303009 | ||||||
chr12:4303178 | C | T | 10 | a0001c0001t0023 a0001c0001t0026 a0001c0001t0028 others(7): Show |
17 | HG01192.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3169C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3169 | chr12 | 4303178 | ||||||
chr12:4303240 | G | A | 1 | a0001c0001t0078 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3231 | chr12 | 4303240 | ||||||
chr12:4303292 | C | A | 1 | a0001c0001t0037 | 2 | HG03654.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3283C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3283 | chr12 | 4303292 | ||||||
chr12:4303372 | G | T | 1 | a0001c0001t0050 | 2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3363G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3363 | chr12 | 4303372 | ||||||
chr12:4303501 | G | A | 1 | a0001c0001t0087 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3492G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3492 | chr12 | 4303501 | ||||||
chr12:4303596 | A | G | 17 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0013 others(14): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3587A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3587 | chr12 | 4303596 | ||||||
chr12:4303647 | T | C | 1 | a0001c0001t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3638T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3638 | chr12 | 4303647 | ||||||
chr12:4303741 | G | A | 1 | a0001c0001t0075 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3732G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3732 | chr12 | 4303741 | ||||||
chr12:4303821 | C | T | 1 | a0001c0001t0080 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3812C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3812 | chr12 | 4303821 | ||||||
chr12:4303834 | T | C | 12 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0032 others(9): Show |
49 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3825T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3825 | chr12 | 4303834 | ||||||
chr12:4303924 | AGAG | A | 3 | a0001c0001t0015 a0001c0001t0019 a0001c0001t0091 |
13 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3919_*3921delGAG | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3919 | INFO_REALIGN_3_PRIME | chr12 | 4303924 | |||||
chr12:4303992 | C | T | 1 | a0001c0001t0032 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3983C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 3983 | chr12 | 4303992 | ||||||
chr12:4304372 | C | G | 3 | a0001c0001t0040 a0001c0001t0048 a0001c0002t0040 |
4 | HG02572.hp2 HG02622.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4363C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 4363 | chr12 | 4304372 | ||||||
chr12:4304754 | G | C | 1 | a0001c0001t0053 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4745G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 4745 | chr12 | 4304754 | ||||||
chr12:4304960 | G | A | 115 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(112): Show |
453 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(450): Show |
3_prime_UTR_variant | MODIFIER | c.*4951G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 4951 | chr12 | 4304960 | ||||||
chr12:4304978 | CT | C | 42 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 others(39): Show |
139 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*4979delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 4979 | INFO_REALIGN_3_PRIME | chr12 | 4304978 | |||||
chr12:4304983 | TTTTTTCT others(4): Show |
T | 1 | a0001c0001t0076 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4985_*4995delCTTT others(7): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 4985 | INFO_REALIGN_3_PRIME | chr12 | 4304983 | |||||
chr12:4305000 | CT | C | 52 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(49): Show |
200 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*5002delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 5002 | INFO_REALIGN_3_PRIME | chr12 | 4305000 | |||||
chr12:4305047 | G | A | 3 | a0001c0001t0079 a0001c0001t0083 a0001c0002t0055 |
3 | HG00408.hp2 NA18981.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5038G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 5/5 | 5038 | chr12 | 4305047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4274290 | C | T | 1 | a0001c0001t0050g0373 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.195+55C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274290 | |||||||
chr12:4274504 | A | C | 2 | a0001c0001t0026g0371 a0001c0001t0026g0372 |
2 | HG01192.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.195+269A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274504 | |||||||
chr12:4274529 | C | A | 1 | a0001c0001t0012g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.195+294C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274529 | |||||||
chr12:4274529 | C | G | 1 | a0001c0001t0003g0370 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.195+294C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274529 | |||||||
chr12:4274530 | C | T | 1 | a0001c0002t0056g0369 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+295C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274530 | |||||||
chr12:4274633 | C | G | 1 | a0001c0001t0001g0368 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.195+398C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274633 | |||||||
chr12:4274743 | G | T | 1 | a0001c0001t0010g0367 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.195+508G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4274743 | |||||||
chr12:4275078 | A | G | 1 | a0001c0001t0006g0366 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.195+843A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275078 | |||||||
chr12:4275101 | C | T | 1 | a0001c0001t0032g0059 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.195+866C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275101 | |||||||
chr12:4275242 | C | A | 1 | a0001c0001t0060g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.196-763C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275242 | |||||||
chr12:4275306 | C | T | 1 | a0001c0001t0038g0365 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.196-699C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275306 | |||||||
chr12:4275392 | A | G | 7 | a0001c0001t0001g0359 a0001c0001t0002g0058 a0001c0001t0002g0361 others(4): Show |
8 | NA18953.hp2 NA18955.hp2 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-613A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275392 | |||||||
chr12:4275459 | C | T | 5 | a0001c0001t0020g0357 a0001c0001t0024g0016 a0001c0001t0024g0358 others(2): Show |
6 | HG02615.hp1 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-546C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275459 | |||||||
chr12:4275497 | G | GC | 16 | a0001c0001t0001g0350 a0001c0001t0002g0341 a0001c0001t0002g0342 others(13): Show |
16 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.196-501dupC | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 4275497 | ||||||
chr12:4275503 | C | T | 6 | a0001c0001t0003g0004 a0001c0001t0003g0354 a0001c0001t0003g0355 others(3): Show |
8 | HG00140.hp1 HG00741.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-502C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275503 | |||||||
chr12:4275530 | C | T | 11 | a0001c0001t0003g0004 a0001c0001t0003g0337 a0001c0001t0003g0354 others(8): Show |
14 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-475C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275530 | |||||||
chr12:4275674 | G | T | 1 | a0001c0001t0006g0334 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.196-331G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275674 | |||||||
chr12:4275678 | T | G | 1 | a0001c0001t0005g0062 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.196-327T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275678 | |||||||
chr12:4275765 | A | G | 1 | a0001c0001t0091g0333 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.196-240A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275765 | |||||||
chr12:4275901 | A | T | 3 | a0001c0001t0001g0368 a0001c0001t0002g0332 a0001c0001t0008g0331 |
3 | HG01346.hp2 HG01952.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.196-104A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 1/4 | chr12 | 4275901 | |||||||
chr12:4276390 | T | A | 1 | a0001c0002t0001g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.411+170T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276390 | |||||||
chr12:4276391 | A | T | 1 | a0001c0002t0001g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.411+171A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276391 | |||||||
chr12:4276411 | A | G | 1 | a0001c0001t0049g0056 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.411+191A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276411 | |||||||
chr12:4276590 | G | A | 1 | a0001c0001t0062g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.411+370G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276590 | |||||||
chr12:4276636 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0021g0330 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+416C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276636 | |||||||
chr12:4276715 | G | C | 2 | a0001c0001t0010g0065 a0001c0001t0059g0066 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.411+495G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276715 | |||||||
chr12:4276876 | C | G | 1 | a0001c0001t0001g0328 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.411+656C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276876 | |||||||
chr12:4276898 | A | G | 12 | a0001c0001t0003g0004 a0001c0001t0003g0327 a0001c0001t0003g0337 others(9): Show |
14 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.411+678A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276898 | |||||||
chr12:4276920 | G | A | 1 | a0001c0001t0045g0067 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.411+700G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4276920 | |||||||
chr12:4277164 | T | C | 1 | a0001c0001t0034g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.411+944T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277164 | |||||||
chr12:4277209 | T | A | 1 | a0001c0002t0051g0069 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.411+989T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277209 | |||||||
chr12:4277231 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.411+1011C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277231 | |||||||
chr12:4277330 | G | T | 1 | a0001c0001t0015g0324 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.411+1110G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277330 | |||||||
chr12:4277403 | A | C | 381 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(378): Show |
436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
intron_variant | MODIFIER | c.411+1183A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277403 | |||||||
chr12:4277607 | G | C | 2 | a0001c0001t0006g0057 a0001c0001t0050g0083 |
3 | HG01884.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.412-1153G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277607 | |||||||
chr12:4277709 | C | T | 1 | a0001c0001t0003g0323 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.412-1051C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277709 | |||||||
chr12:4277734 | G | A | 2 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
2 | HG03490.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.412-1026G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277734 | |||||||
chr12:4277894 | G | C | 1 | a0001c0001t0031g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.412-866G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4277894 | |||||||
chr12:4277985 | C | CAA | 201 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(198): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.412-774_412-773dup others(2): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 4277985 | ||||||
chr12:4278004 | G | A | 1 | a0001c0001t0003g0354 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.412-756G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278004 | |||||||
chr12:4278019 | C | T | 1 | a0001c0002t0026g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.412-741C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278019 | |||||||
chr12:4278147 | G | T | 1 | a0001c0001t0025g0216 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.412-613G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278147 | |||||||
chr12:4278273 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.412-487G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278273 | |||||||
chr12:4278274 | G | A | 3 | a0001c0001t0006g0057 a0001c0001t0034g0068 a0001c0001t0050g0083 |
4 | HG01884.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-486G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278274 | |||||||
chr12:4278448 | T | G | 1 | a0001c0001t0049g0056 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.412-312T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278448 | |||||||
chr12:4278471 | G | T | 1 | a0001c0002t0010g0215 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.412-289G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278471 | |||||||
chr12:4278583 | C | A | 5 | a0001c0001t0004g0087 a0001c0002t0004g0089 a0001c0002t0004g0339 others(2): Show |
6 | NA18957.hp2 NA18961.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-177C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278583 | |||||||
chr12:4278652 | C | T | 3 | a0001c0001t0024g0016 a0001c0001t0024g0358 a0001c0001t0074g0016 |
4 | HG02615.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-108C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278652 | |||||||
chr12:4278685 | C | T | 1 | a0001c0001t0014g0322 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.412-75C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 2/4 | chr12 | 4278685 | |||||||
chr12:4278993 | C | T | 1 | a0001c0001t0058g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.571+74C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4278993 | |||||||
chr12:4279006 | AT | A | 5 | a0001c0001t0009g0070 a0001c0001t0009g0072 a0001c0001t0017g0071 others(2): Show |
6 | HG02615.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+91delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4279006 | ||||||
chr12:4279087 | A | G | 1 | a0001c0001t0048g0338 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.571+168A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279087 | |||||||
chr12:4279105 | C | T | 17 | a0001c0001t0066g0042 a0001c0002t0001g0015 a0001c0002t0001g0063 others(14): Show |
19 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.571+186C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279105 | |||||||
chr12:4279158 | A | C | 1 | a0001c0001t0006g0057 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.571+239A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279158 | |||||||
chr12:4279203 | T | C | 1 | a0001c0001t0023g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571+284T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279203 | |||||||
chr12:4279366 | A | G | 41 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(38): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.571+447A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279366 | |||||||
chr12:4279394 | C | CT | 8 | a0001c0001t0010g0352 a0001c0001t0024g0016 a0001c0001t0024g0358 others(5): Show |
9 | HG01192.hp1 HG01192.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+491dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4279394 | ||||||
chr12:4279394 | C | CTT | 11 | a0001c0001t0001g0329 a0001c0001t0001g0368 a0001c0001t0002g0332 others(8): Show |
11 | HG01346.hp2 HG01358.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.571+490_571+491dup others(2): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4279394 | ||||||
chr12:4279394 | C | T | 1 | a0001c0002t0012g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.571+475C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279394 | |||||||
chr12:4279394 | CT | C | 90 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(87): Show |
99 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.571+491delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4279394 | ||||||
chr12:4279449 | C | T | 1 | a0001c0001t0048g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.571+530C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279449 | |||||||
chr12:4279496 | G | A | 1 | a0001c0001t0015g0220 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.571+577G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279496 | |||||||
chr12:4279595 | CCACGTG | C | 35 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(32): Show |
37 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.571+677_571+682del others(6): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279595 | |||||||
chr12:4279598 | C | T | 1 | a0001c0001t0031g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.571+679C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279598 | |||||||
chr12:4279603 | A | T | 35 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(32): Show |
37 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.571+684A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279603 | |||||||
chr12:4279606 | CCACAATT others(551): Show |
C | 35 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(32): Show |
37 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.571+688_571+1245de others(1): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279606 | |||||||
chr12:4279748 | A | G | 41 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(38): Show |
50 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.571+829A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279748 | |||||||
chr12:4279775 | T | C | 1 | a0001c0001t0008g0007 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.571+856T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279775 | |||||||
chr12:4279811 | A | G | 1 | a0001c0002t0002g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571+892A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279811 | |||||||
chr12:4279868 | C | T | 6 | a0001c0002t0017g0025 a0001c0002t0017g0116 a0001c0002t0034g0115 others(3): Show |
7 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+949C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279868 | |||||||
chr12:4279978 | G | A | 1 | a0001c0002t0007g0135 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.571+1059G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279978 | |||||||
chr12:4279992 | A | G | 58 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(55): Show |
69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.571+1073A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4279992 | |||||||
chr12:4280024 | C | G | 1 | a0001c0002t0004g0122 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.571+1105C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280024 | |||||||
chr12:4280030 | T | C | 2 | a0001c0001t0048g0172 a0001c0002t0028g0119 |
2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.571+1111T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280030 | |||||||
chr12:4280198 | T | G | 7 | a0001c0001t0008g0097 a0001c0001t0013g0095 a0001c0001t0031g0096 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+1279T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280198 | |||||||
chr12:4280544 | C | T | 1 | a0001c0001t0011g0317 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.571+1625C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280544 | |||||||
chr12:4280593 | G | C | 1 | a0001c0002t0026g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.571+1674G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280593 | |||||||
chr12:4280622 | C | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1703C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280622 | |||||||
chr12:4280623 | C | CCAAGA | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1704_571+1705i others(7): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280623 | |||||||
chr12:4280625 | G | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1706G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280625 | |||||||
chr12:4280626 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1707T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280626 | |||||||
chr12:4280627 | G | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1708G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280627 | |||||||
chr12:4280629 | C | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1710C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280629 | |||||||
chr12:4280630 | C | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1711C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280630 | |||||||
chr12:4280631 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1712T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280631 | |||||||
chr12:4280632 | G | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1713G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280632 | |||||||
chr12:4280633 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1714T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280633 | |||||||
chr12:4280636 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1717T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280636 | |||||||
chr12:4280637 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1718T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280637 | |||||||
chr12:4280638 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1719T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280638 | |||||||
chr12:4280639 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1720T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280639 | |||||||
chr12:4280640 | G | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1721G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280640 | |||||||
chr12:4280641 | T | C | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1722T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280641 | |||||||
chr12:4280643 | T | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1724T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280643 | |||||||
chr12:4280644 | C | G | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1725C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280644 | |||||||
chr12:4280645 | C | A | 4 | a0001c0002t0005g0022 a0001c0002t0005g0100 a0001c0002t0009g0099 others(1): Show |
5 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+1726C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280645 | |||||||
chr12:4280699 | C | T | 1 | a0001c0001t0050g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.571+1780C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280699 | |||||||
chr12:4280867 | T | C | 1 | a0001c0001t0005g0047 | 2 | HG02165.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.571+1948T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280867 | |||||||
chr12:4280884 | G | A | 6 | a0001c0001t0008g0097 a0001c0001t0013g0095 a0001c0001t0031g0096 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+1965G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280884 | |||||||
chr12:4280961 | C | G | 64 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(61): Show |
75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.571+2042C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4280961 | |||||||
chr12:4281160 | T | C | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(60): Show |
74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.571+2241T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281160 | |||||||
chr12:4281161 | C | T | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(60): Show |
74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.571+2242C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281161 | |||||||
chr12:4281168 | T | G | 393 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(390): Show |
449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.571+2249T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281168 | |||||||
chr12:4281206 | T | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(42): Show |
54 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.571+2287T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281206 | |||||||
chr12:4281280 | T | A | 1 | a0001c0001t0013g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.571+2361T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281280 | |||||||
chr12:4281303 | C | T | 2 | a0001c0001t0012g0139 a0001c0001t0040g0140 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.571+2384C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281303 | |||||||
chr12:4281448 | G | A | 1 | a0001c0001t0017g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.571+2529G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281448 | |||||||
chr12:4281499 | G | A | 16 | a0001c0001t0002g0223 a0001c0001t0003g0006 a0001c0001t0003g0222 others(13): Show |
17 | HG00597.hp1 HG02015.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.571+2580G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281499 | |||||||
chr12:4281508 | C | T | 34 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(31): Show |
37 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.571+2589C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281508 | |||||||
chr12:4281512 | C | T | 1 | a0001c0001t0034g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.571+2593C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281512 | |||||||
chr12:4281529 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.571+2610G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281529 | |||||||
chr12:4281540 | T | C | 1 | a0001c0001t0001g0048 | 2 | NA18952.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.571+2621T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281540 | |||||||
chr12:4281591 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.571+2672C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281591 | |||||||
chr12:4281647 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0170 |
3 | NA18948.hp2 NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.571+2728C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281647 | |||||||
chr12:4281930 | A | G | 1 | a0001c0002t0002g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571+3011A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4281930 | |||||||
chr12:4282058 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.571+3139G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282058 | |||||||
chr12:4282105 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.571+3186T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282105 | |||||||
chr12:4282124 | G | A | 1 | a0001c0001t0004g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.571+3205G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282124 | |||||||
chr12:4282166 | C | T | 5 | a0001c0001t0010g0065 a0001c0001t0039g0138 a0001c0001t0058g0214 others(2): Show |
5 | HG01358.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.571+3247C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282166 | |||||||
chr12:4282217 | C | T | 1 | a0001c0001t0006g0057 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.571+3298C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282217 | |||||||
chr12:4282225 | G | A | 1 | a0001c0002t0010g0215 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571+3306G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282225 | |||||||
chr12:4282330 | G | A | 2 | a0001c0001t0021g0174 a0001c0001t0093g0173 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.571+3411G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282330 | |||||||
chr12:4282343 | A | G | 1 | a0001c0001t0007g0311 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.571+3424A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282343 | |||||||
chr12:4282451 | A | C | 2 | a0001c0001t0002g0218 a0001c0001t0028g0137 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.571+3532A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282451 | |||||||
chr12:4282623 | C | T | 4 | a0001c0002t0005g0028 a0001c0002t0005g0136 a0001c0002t0007g0135 others(1): Show |
4 | NA18980.hp2 NA19068.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+3704C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282623 | |||||||
chr12:4282860 | A | G | 1 | a0001c0001t0038g0203 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.571+3941A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282860 | |||||||
chr12:4282986 | G | C | 2 | a0001c0001t0002g0218 a0001c0001t0028g0137 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.571+4067G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4282986 | |||||||
chr12:4283126 | C | T | 1 | a0001c0002t0004g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.571+4207C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283126 | |||||||
chr12:4283207 | C | G | 1 | a0001c0001t0050g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.571+4288C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283207 | |||||||
chr12:4283225 | C | A | 117 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(114): Show |
139 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.571+4306C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283225 | |||||||
chr12:4283296 | G | A | 1 | a0001c0001t0070g0076 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.571+4377G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283296 | |||||||
chr12:4283332 | C | T | 3 | a0001c0002t0001g0015 a0001c0002t0001g0063 a0001c0002t0045g0015 |
4 | NA18944.hp2 NA18962.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+4413C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283332 | |||||||
chr12:4283364 | C | T | 40 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(37): Show |
49 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.571+4445C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283364 | |||||||
chr12:4283779 | C | T | 1 | a0001c0002t0012g0346 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.571+4860C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283779 | |||||||
chr12:4283877 | C | T | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+4958C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4283877 | |||||||
chr12:4284031 | C | T | 1 | a0001c0001t0031g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.572-4811C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284031 | |||||||
chr12:4284240 | G | C | 1 | a0001c0001t0012g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.572-4602G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284240 | |||||||
chr12:4284308 | A | G | 306 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(303): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.572-4534A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284308 | |||||||
chr12:4284377 | C | T | 26 | a0001c0001t0001g0090 a0001c0001t0001g0329 a0001c0001t0002g0332 others(23): Show |
30 | HG01346.hp2 HG01358.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.572-4465C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284377 | |||||||
chr12:4284377 | CCTT | C | 7 | a0001c0001t0009g0070 a0001c0002t0017g0025 a0001c0002t0017g0116 others(4): Show |
8 | HG02622.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-4462_572-4460d others(5): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4284377 | ||||||
chr12:4284497 | G | A | 26 | a0001c0001t0001g0090 a0001c0001t0001g0329 a0001c0001t0002g0332 others(23): Show |
30 | HG01346.hp2 HG01358.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.572-4345G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284497 | |||||||
chr12:4284643 | C | T | 6 | a0001c0001t0002g0223 a0001c0001t0003g0006 a0001c0001t0003g0225 others(3): Show |
7 | NA18940.hp1 NA18945.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.572-4199C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284643 | |||||||
chr12:4284711 | A | G | 1 | a0001c0002t0005g0209 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.572-4131A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284711 | |||||||
chr12:4284721 | C | CT | 97 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(94): Show |
108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.572-4110dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4284721 | ||||||
chr12:4284733 | C | A | 2 | a0001c0001t0004g0250 a0001c0001t0004g0251 |
2 | HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.572-4109C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284733 | |||||||
chr12:4284744 | C | CT | 248 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(245): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.572-4086dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4284744 | ||||||
chr12:4284744 | C | CTT | 9 | a0001c0001t0010g0065 a0001c0001t0021g0174 a0001c0001t0022g0001 others(6): Show |
9 | HG01358.hp1 HG01928.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.572-4087_572-4086d others(4): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4284744 | ||||||
chr12:4284851 | C | T | 305 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(302): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.572-3991C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284851 | |||||||
chr12:4284987 | C | T | 1 | a0001c0002t0005g0136 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.572-3855C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4284987 | |||||||
chr12:4285026 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.572-3816C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285026 | |||||||
chr12:4285201 | C | A | 1 | a0001c0002t0028g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.572-3641C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285201 | |||||||
chr12:4285227 | G | A | 3 | a0001c0002t0001g0051 a0001c0002t0004g0051 a0001c0002t0004g0261 |
3 | NA18951.hp1 NA19010.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.572-3615G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285227 | |||||||
chr12:4285408 | C | T | 2 | a0001c0001t0006g0040 a0001c0001t0030g0040 |
2 | NA18954.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.572-3434C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285408 | |||||||
chr12:4285711 | T | C | 54 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(51): Show |
63 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.572-3131T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285711 | |||||||
chr12:4285720 | C | T | 2 | a0001c0001t0006g0024 a0001c0001t0006g0106 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.572-3122C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285720 | |||||||
chr12:4285879 | G | A | 1 | a0001c0001t0003g0327 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.572-2963G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285879 | |||||||
chr12:4285924 | G | A | 1 | a0001c0001t0034g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.572-2918G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4285924 | |||||||
chr12:4286477 | C | G | 1 | a0001c0001t0021g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.572-2365C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286477 | |||||||
chr12:4286489 | G | A | 1 | a0001c0001t0027g0262 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.572-2353G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286489 | |||||||
chr12:4286492 | G | T | 1 | a0001c0001t0034g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.572-2350G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286492 | |||||||
chr12:4286494 | G | A | 1 | a0001c0002t0004g0120 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.572-2348G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286494 | |||||||
chr12:4286694 | G | A | 1 | a0001c0001t0014g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.572-2148G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286694 | |||||||
chr12:4286699 | G | T | 50 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(47): Show |
56 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.572-2143G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286699 | |||||||
chr12:4286719 | C | T | 33 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(30): Show |
35 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.572-2123C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286719 | |||||||
chr12:4286817 | G | C | 1 | a0001c0001t0031g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.572-2025G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286817 | |||||||
chr12:4286819 | A | T | 7 | a0001c0001t0007g0001 a0001c0001t0007g0311 a0001c0001t0022g0001 others(4): Show |
12 | HG01928.hp1 HG01928.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.572-2023A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286819 | |||||||
chr12:4286914 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0087g0046 |
2 | HG00544.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.572-1928C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286914 | |||||||
chr12:4286944 | G | A | 1 | a0001c0002t0003g0102 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.572-1898G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286944 | |||||||
chr12:4286975 | G | C | 1 | a0001c0001t0015g0324 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.572-1867G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4286975 | |||||||
chr12:4287086 | C | T | 2 | a0001c0001t0012g0075 a0001c0001t0031g0086 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.572-1756C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287086 | |||||||
chr12:4287392 | G | A | 1 | a0001c0001t0009g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.572-1450G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287392 | |||||||
chr12:4287478 | G | A | 1 | a0001c0001t0006g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.572-1364G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287478 | |||||||
chr12:4287502 | G | A | 5 | a0001c0001t0010g0065 a0001c0001t0039g0138 a0001c0001t0058g0214 others(2): Show |
5 | HG01358.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.572-1340G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287502 | |||||||
chr12:4287540 | C | T | 3 | a0001c0001t0001g0329 a0001c0001t0031g0096 a0001c0002t0026g0094 |
3 | HG02559.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.572-1302C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287540 | |||||||
chr12:4287580 | G | A | 26 | a0001c0001t0001g0329 a0001c0001t0002g0332 a0001c0001t0006g0057 others(23): Show |
30 | HG01346.hp2 HG01358.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.572-1262G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287580 | |||||||
chr12:4287585 | G | A | 1 | a0001c0001t0021g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.572-1257G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287585 | |||||||
chr12:4287681 | C | T | 1 | a0001c0001t0028g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.572-1161C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287681 | |||||||
chr12:4287808 | C | G | 1 | a0001c0001t0009g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.572-1034C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287808 | |||||||
chr12:4287866 | G | A | 1 | a0001c0001t0039g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.572-976G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287866 | |||||||
chr12:4287888 | C | G | 1 | a0001c0001t0021g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.572-954C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287888 | |||||||
chr12:4287909 | C | G | 1 | a0001c0001t0031g0096 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.572-933C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4287909 | |||||||
chr12:4288057 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0012g0060 a0001c0001t0019g0306 |
3 | HG03017.hp2 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.572-785C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4288057 | |||||||
chr12:4288181 | C | T | 1 | a0001c0002t0005g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.572-661C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4288181 | |||||||
chr12:4288187 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.572-655C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4288187 | |||||||
chr12:4288237 | CT | C | 239 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(236): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.572-589delT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4288237 | ||||||
chr12:4288237 | CTT | C | 50 | a0001c0001t0001g0090 a0001c0001t0002g0218 a0001c0001t0003g0004 others(47): Show |
59 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.572-590_572-589del others(2): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 4288237 | ||||||
chr12:4288262 | G | A | 1 | a0001c0002t0026g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.572-580G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4288262 | |||||||
chr12:4288540 | T | A | 8 | a0001c0001t0006g0077 a0001c0001t0009g0072 a0001c0001t0017g0071 others(5): Show |
9 | HG01891.hp2 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.572-302T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4288540 | |||||||
chr12:4288600 | G | C | 44 | a0001c0001t0004g0087 a0001c0001t0005g0092 a0001c0001t0005g0244 others(41): Show |
52 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.572-242G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 3/4 | chr12 | 4288600 | |||||||
chr12:4289107 | C | T | 1 | a0001c0001t0009g0248 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.720+117C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289107 | |||||||
chr12:4289174 | G | A | 1 | a0001c0001t0025g0227 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.720+184G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289174 | |||||||
chr12:4289183 | CG | C | 149 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(146): Show |
166 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.720+195delG | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4289183 | ||||||
chr12:4289284 | T | C | 2 | a0001c0001t0008g0331 a0001c0001t0021g0330 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.720+294T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289284 | |||||||
chr12:4289331 | C | T | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(50): Show |
62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.720+341C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289331 | |||||||
chr12:4289396 | C | G | 34 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0319 others(31): Show |
36 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.720+406C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289396 | |||||||
chr12:4289408 | G | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0361 a0001c0001t0002g0362 others(1): Show |
5 | NA18995.hp1 NA18997.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+418G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289408 | |||||||
chr12:4289453 | G | A | 1 | a0001c0002t0004g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720+463G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289453 | |||||||
chr12:4289460 | G | T | 2 | a0001c0001t0066g0042 a0001c0002t0010g0042 |
2 | HG00323.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.720+470G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289460 | |||||||
chr12:4289870 | A | G | 296 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(293): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.720+880A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289870 | |||||||
chr12:4289884 | A | G | 182 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(179): Show |
206 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.720+894A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289884 | |||||||
chr12:4289888 | C | T | 42 | a0001c0001t0004g0087 a0001c0001t0005g0092 a0001c0001t0005g0244 others(39): Show |
50 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.720+898C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289888 | |||||||
chr12:4289921 | T | G | 95 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(92): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.720+931T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289921 | |||||||
chr12:4289929 | G | C | 1 | a0001c0002t0005g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720+939G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289929 | |||||||
chr12:4289982 | G | C | 1 | a0001c0001t0002g0361 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.720+992G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4289982 | |||||||
chr12:4290075 | G | A | 1 | a0001c0001t0048g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.720+1085G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290075 | |||||||
chr12:4290272 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.720+1282G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290272 | |||||||
chr12:4290330 | C | T | 75 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(72): Show |
90 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.720+1340C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290330 | |||||||
chr12:4290453 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.720+1463C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290453 | |||||||
chr12:4290511 | G | T | 1 | a0001c0001t0021g0295 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720+1521G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290511 | |||||||
chr12:4290566 | G | C | 1 | a0001c0001t0008g0204 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.720+1576G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290566 | |||||||
chr12:4290572 | GA | G | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(44): Show |
56 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.720+1584delA | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4290572 | ||||||
chr12:4290617 | T | TC | 75 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(72): Show |
80 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.720+1632dupC | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4290617 | ||||||
chr12:4290623 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.720+1633G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290623 | |||||||
chr12:4290662 | C | G | 1 | a0001c0002t0005g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.720+1672C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290662 | |||||||
chr12:4290751 | G | A | 340 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(337): Show |
389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.720+1761G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290751 | |||||||
chr12:4290752 | A | C | 340 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(337): Show |
389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.720+1762A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290752 | |||||||
chr12:4290767 | C | T | 1 | a0001c0001t0015g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.720+1777C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290767 | |||||||
chr12:4290772 | C | A | 1 | a0001c0001t0030g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.720+1782C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290772 | |||||||
chr12:4290798 | A | T | 1 | a0001c0001t0012g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.720+1808A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290798 | |||||||
chr12:4290804 | G | A | 294 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(291): Show |
334 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.720+1814G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290804 | |||||||
chr12:4290887 | G | A | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1897G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290887 | |||||||
chr12:4290945 | C | T | 254 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.720+1955C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290945 | |||||||
chr12:4290968 | G | A | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1978G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290968 | |||||||
chr12:4290978 | C | T | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1988C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290978 | |||||||
chr12:4290998 | G | A | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2008G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4290998 | |||||||
chr12:4291014 | G | A | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2024G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291014 | |||||||
chr12:4291019 | A | G | 4 | a0001c0001t0008g0097 a0001c0001t0050g0083 a0001c0001t0071g0021 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2029A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291019 | |||||||
chr12:4291062 | C | T | 1 | a0001c0001t0010g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.720+2072C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291062 | |||||||
chr12:4291207 | C | CTGTGTG | 18 | a0001c0001t0002g0218 a0001c0001t0006g0077 a0001c0001t0009g0070 others(15): Show |
20 | HG01361.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.720+2239_720+2244d others(8): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(3): Show |
38 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(35): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.720+2235_720+2244d others(12): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(5): Show |
39 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0232 others(36): Show |
52 | HG00597.hp1 HG00639.hp2 HG01928.hp1 others(49): Show |
intron_variant | MODIFIER | c.720+2233_720+2244d others(14): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(7): Show |
39 | a0001c0001t0001g0368 a0001c0001t0002g0223 a0001c0001t0003g0004 others(36): Show |
49 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.720+2231_720+2244d others(16): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(9): Show |
14 | a0001c0001t0005g0294 a0001c0001t0008g0356 a0001c0001t0010g0023 others(11): Show |
15 | HG01081.hp2 HG01256.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+2229_720+2244d others(18): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(11): Show |
18 | a0001c0001t0001g0111 a0001c0001t0001g0319 a0001c0001t0002g0304 others(15): Show |
19 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.720+2227_720+2244d others(20): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(13): Show |
27 | a0001c0001t0001g0196 a0001c0001t0002g0170 a0001c0001t0003g0043 others(24): Show |
28 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.720+2225_720+2244d others(22): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(15): Show |
50 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0001t0001g0181 others(47): Show |
54 | HG00438.hp2 HG00735.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.720+2223_720+2244d others(24): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(17): Show |
60 | a0001c0001t0001g0032 a0001c0001t0001g0163 a0001c0001t0001g0350 others(57): Show |
74 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.720+2221_720+2244d others(26): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(19): Show |
41 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(38): Show |
45 | HG00558.hp2 HG01109.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.720+2219_720+2244d others(28): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(21): Show |
21 | a0001c0001t0001g0153 a0001c0001t0002g0029 a0001c0001t0002g0155 others(18): Show |
23 | HG00558.hp1 HG00741.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.720+2244_720+2245i others(30): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | C | CTGTGTGT others(23): Show |
7 | a0001c0001t0004g0151 a0001c0001t0005g0244 a0001c0001t0005g0308 others(4): Show |
7 | HG00621.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+2244_720+2245i others(32): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291207 | CTGTGTGT others(1): Show |
C | 2 | a0001c0001t0003g0012 a0001c0001t0016g0012 |
3 | HG01257.hp2 HG01258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.720+2237_720+2244d others(10): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291207 | ||||||
chr12:4291234 | T | TGTGTGTG others(6): Show |
1 | a0001c0002t0007g0252 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.720+2244_720+2245i others(15): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291234 | |||||||
chr12:4291234 | T | TGTGTGTG others(8): Show |
2 | a0001c0001t0003g0084 a0001c0001t0003g0355 |
2 | HG02148.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.720+2244_720+2245i others(17): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291234 | |||||||
chr12:4291234 | T | TGTGTGTG others(16): Show |
2 | a0001c0001t0015g0142 a0001c0002t0007g0133 |
2 | HG00544.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.720+2244_720+2245i others(25): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291234 | |||||||
chr12:4291234 | T | TGTGTGTG others(18): Show |
3 | a0001c0001t0001g0240 a0001c0001t0012g0320 a0001c0001t0043g0079 |
3 | HG01891.hp1 NA18977.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.720+2244_720+2245i others(27): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291234 | |||||||
chr12:4291234 | T | TGTGTGTG others(20): Show |
4 | a0001c0001t0001g0030 a0001c0001t0002g0152 a0001c0001t0025g0030 others(1): Show |
4 | HG01981.hp1 HG02004.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2244_720+2245i others(29): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291234 | |||||||
chr12:4291234 | T | TGTGTGTG others(22): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0149 |
2 | NA18959.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.720+2244_720+2245i others(31): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291234 | |||||||
chr12:4291244 | T | G | 1 | a0001c0001t0017g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.720+2254T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291244 | |||||||
chr12:4291251 | G | A | 1 | a0001c0001t0015g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.720+2261G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291251 | |||||||
chr12:4291403 | C | A | 327 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(324): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.720+2413C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291403 | |||||||
chr12:4291409 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.720+2419G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291409 | |||||||
chr12:4291446 | G | GA | 10 | a0001c0001t0008g0097 a0001c0001t0010g0065 a0001c0001t0039g0138 others(7): Show |
10 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+2458dupA | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4291446 | ||||||
chr12:4291465 | G | T | 2 | a0001c0001t0048g0172 a0001c0001t0048g0338 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.720+2475G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291465 | |||||||
chr12:4291614 | C | T | 1 | a0001c0001t0019g0306 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.720+2624C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291614 | |||||||
chr12:4291642 | C | T | 186 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(183): Show |
210 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.720+2652C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291642 | |||||||
chr12:4291840 | C | T | 2 | a0001c0001t0010g0074 a0001c0001t0034g0068 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.720+2850C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291840 | |||||||
chr12:4291867 | G | A | 400 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(397): Show |
457 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(454): Show |
intron_variant | MODIFIER | c.720+2877G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291867 | |||||||
chr12:4291987 | G | A | 1 | a0001c0001t0014g0322 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.720+2997G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4291987 | |||||||
chr12:4292035 | T | C | 67 | a0001c0001t0001g0196 a0001c0001t0001g0319 a0001c0001t0002g0039 others(64): Show |
82 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.720+3045T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292035 | |||||||
chr12:4292176 | G | GAT | 6 | a0001c0001t0005g0294 a0001c0001t0021g0174 a0001c0001t0026g0371 others(3): Show |
6 | HG01192.hp2 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+3197_720+3198d others(4): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4292176 | ||||||
chr12:4292453 | C | T | 1 | a0001c0001t0064g0284 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.720+3463C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292453 | |||||||
chr12:4292468 | G | A | 1 | a0001c0001t0006g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.720+3478G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292468 | |||||||
chr12:4292488 | T | C | 2 | a0001c0002t0028g0119 a0001c0002t0034g0115 |
2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.720+3498T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292488 | |||||||
chr12:4292639 | C | T | 1 | a0001c0001t0050g0373 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.720+3649C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292639 | |||||||
chr12:4292676 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0004g0272 a0001c0001t0027g0264 |
3 | NA18965.hp1 NA19005.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.720+3686G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292676 | |||||||
chr12:4292730 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.720+3740T>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292730 | |||||||
chr12:4292762 | G | C | 1 | a0001c0001t0093g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.720+3772G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292762 | |||||||
chr12:4292891 | C | T | 1 | a0001c0001t0080g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.720+3901C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292891 | |||||||
chr12:4292960 | C | A | 1 | a0001c0002t0040g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.720+3970C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4292960 | |||||||
chr12:4293369 | A | C | 2 | a0001c0002t0002g0177 a0001c0002t0065g0118 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.720+4379A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293369 | |||||||
chr12:4293458 | C | T | 1 | a0001c0001t0003g0340 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.720+4468C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293458 | |||||||
chr12:4293522 | A | G | 102 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(99): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.720+4532A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293522 | |||||||
chr12:4293574 | C | A | 1 | a0001c0001t0002g0190 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.720+4584C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293574 | |||||||
chr12:4293651 | A | G | 101 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(98): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.720+4661A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293651 | |||||||
chr12:4293669 | G | A | 3 | a0001c0001t0048g0172 a0001c0001t0048g0338 a0001c0001t0050g0373 |
3 | HG02622.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+4679G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293669 | |||||||
chr12:4293681 | C | T | 1 | a0001c0002t0005g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720+4691C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293681 | |||||||
chr12:4293783 | A | G | 1 | a0001c0002t0034g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.720+4793A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293783 | |||||||
chr12:4293842 | C | T | 1 | a0001c0002t0012g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.720+4852C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293842 | |||||||
chr12:4293893 | G | A | 1 | a0001c0001t0028g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.720+4903G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293893 | |||||||
chr12:4293903 | C | T | 1 | a0001c0001t0050g0373 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.720+4913C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293903 | |||||||
chr12:4293948 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.720+4958C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4293948 | |||||||
chr12:4294036 | G | A | 2 | a0001c0001t0003g0191 a0001c0001t0006g0192 |
2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.720+5046G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294036 | |||||||
chr12:4294037 | C | T | 1 | a0001c0001t0046g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.720+5047C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294037 | |||||||
chr12:4294313 | A | G | 1 | a0001c0001t0049g0056 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.720+5323A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294313 | |||||||
chr12:4294341 | G | C | 390 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(387): Show |
447 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
intron_variant | MODIFIER | c.720+5351G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294341 | |||||||
chr12:4294341 | G | T | 4 | a0001c0001t0015g0176 a0001c0001t0026g0371 a0001c0001t0026g0372 others(1): Show |
4 | HG01192.hp2 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+5351G>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294341 | |||||||
chr12:4294416 | G | A | 1 | a0001c0001t0011g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.720+5426G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294416 | |||||||
chr12:4294605 | A | G | 371 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(368): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.721-5255A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294605 | |||||||
chr12:4294645 | C | T | 12 | a0001c0001t0006g0077 a0001c0001t0023g0018 a0001c0001t0023g0073 others(9): Show |
14 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.721-5215C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294645 | |||||||
chr12:4294684 | C | G | 12 | a0001c0001t0005g0294 a0001c0001t0017g0249 a0001c0001t0021g0174 others(9): Show |
13 | HG01261.hp2 HG02055.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-5176C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294684 | |||||||
chr12:4294698 | G | A | 31 | a0001c0001t0001g0196 a0001c0001t0001g0319 a0001c0001t0002g0039 others(28): Show |
32 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.721-5162G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294698 | |||||||
chr12:4294710 | C | T | 9 | a0001c0001t0003g0004 a0001c0001t0003g0104 a0001c0001t0003g0354 others(6): Show |
11 | HG00140.hp1 HG00741.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-5150C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294710 | |||||||
chr12:4294865 | A | T | 3 | a0001c0001t0010g0065 a0001c0001t0059g0066 a0001c0001t0086g0336 |
3 | HG01358.hp1 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-4995A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294865 | |||||||
chr12:4294927 | G | A | 2 | a0001c0001t0009g0072 a0001c0001t0017g0071 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.721-4933G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294927 | |||||||
chr12:4294992 | G | A | 49 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(46): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.721-4868G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4294992 | |||||||
chr12:4295171 | G | A | 1 | a0001c0001t0009g0314 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.721-4689G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4295171 | |||||||
chr12:4295186 | T | C | 4 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0106 others(1): Show |
7 | HG01109.hp1 HG01884.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-4674T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4295186 | |||||||
chr12:4295206 | G | A | 1 | a0001c0001t0070g0076 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-4654G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4295206 | |||||||
chr12:4295210 | A | G | 50 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0012 others(47): Show |
61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.721-4650A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4295210 | |||||||
chr12:4295260 | G | A | 2 | a0001c0001t0034g0068 a0001c0001t0084g0310 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.721-4600G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4295260 | |||||||
chr12:4296215 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0012g0060 a0001c0001t0019g0306 |
3 | HG03017.hp2 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.721-3645C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296215 | |||||||
chr12:4296223 | A | G | 175 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(172): Show |
198 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.721-3637A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296223 | |||||||
chr12:4296251 | C | T | 1 | a0001c0002t0028g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.721-3609C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296251 | |||||||
chr12:4296364 | A | G | 1 | a0001c0002t0004g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.721-3496A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296364 | |||||||
chr12:4296434 | G | A | 2 | a0001c0002t0004g0089 a0001c0002t0004g0339 |
2 | NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.721-3426G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296434 | |||||||
chr12:4296449 | C | T | 18 | a0001c0001t0010g0023 a0001c0001t0016g0023 a0001c0001t0017g0249 others(15): Show |
20 | HG01192.hp2 HG01256.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.721-3411C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296449 | |||||||
chr12:4296456 | C | T | 1 | a0001c0001t0050g0373 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.721-3404C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296456 | |||||||
chr12:4296509 | T | C | 388 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(385): Show |
444 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(441): Show |
intron_variant | MODIFIER | c.721-3351T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296509 | |||||||
chr12:4296518 | G | A | 2 | a0001c0001t0068g0292 a0001c0002t0012g0293 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-3342G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296518 | |||||||
chr12:4296520 | A | G | 230 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(227): Show |
256 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.721-3340A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296520 | |||||||
chr12:4296638 | G | A | 325 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(322): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.721-3222G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296638 | |||||||
chr12:4296684 | T | G | 64 | a0001c0001t0001g0090 a0001c0001t0001g0196 a0001c0001t0001g0319 others(61): Show |
74 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.721-3176T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296684 | |||||||
chr12:4296701 | TG | T | 6 | a0001c0001t0008g0171 a0001c0001t0010g0065 a0001c0001t0010g0199 others(3): Show |
6 | HG01358.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-3155delG | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4296701 | ||||||
chr12:4296704 | GGA | G | 63 | a0001c0001t0001g0113 a0001c0001t0003g0004 a0001c0001t0003g0009 others(60): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.721-3155_721-3154d others(4): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296704 | |||||||
chr12:4296705 | G | GA | 70 | a0001c0001t0001g0237 a0001c0001t0002g0033 a0001c0001t0002g0035 others(67): Show |
75 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.721-3140dupA | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4296705 | ||||||
chr12:4296705 | GA | G | 208 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(205): Show |
241 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.721-3140delA | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4296705 | ||||||
chr12:4296705 | GAA | G | 37 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(34): Show |
39 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.721-3141_721-3140d others(4): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4296705 | ||||||
chr12:4296865 | C | T | 398 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(395): Show |
455 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(452): Show |
intron_variant | MODIFIER | c.721-2995C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296865 | |||||||
chr12:4296910 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.721-2950C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4296910 | |||||||
chr12:4297098 | C | G | 2 | a0001c0001t0004g0282 a0001c0001t0004g0351 |
2 | HG00738.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.721-2762C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297098 | |||||||
chr12:4297115 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0110 others(168): Show |
193 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.721-2745A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297115 | |||||||
chr12:4297161 | T | C | 1 | a0001c0001t0064g0284 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.721-2699T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297161 | |||||||
chr12:4297162 | C | A | 1 | a0001c0001t0064g0284 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.721-2698C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297162 | |||||||
chr12:4297172 | C | CT | 353 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(350): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.721-2686dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297172 | ||||||
chr12:4297178 | C | G | 1 | a0001c0001t0001g0305 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.721-2682C>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297178 | |||||||
chr12:4297372 | A | T | 1 | a0001c0002t0003g0102 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.721-2488A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297372 | |||||||
chr12:4297410 | T | C | 52 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(49): Show |
56 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.721-2450T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297410 | |||||||
chr12:4297416 | C | A | 62 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0009 others(59): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.721-2444C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297416 | |||||||
chr12:4297567 | TC | T | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(45): Show |
52 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.721-2292delC | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297567 | |||||||
chr12:4297568 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.721-2292C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297568 | |||||||
chr12:4297569 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.721-2291T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297569 | |||||||
chr12:4297570 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.721-2290C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297570 | |||||||
chr12:4297570 | C | CA | 78 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0113 others(75): Show |
87 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.721-2263dupA | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297570 | ||||||
chr12:4297570 | C | CAA | 19 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0232 others(16): Show |
21 | HG00558.hp2 HG00597.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-2264_721-2263d others(4): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297570 | ||||||
chr12:4297570 | CA | C | 98 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0044 others(95): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.721-2263delA | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297570 | ||||||
chr12:4297570 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0008g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.721-2274_721-2263d others(14): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297570 | ||||||
chr12:4297584 | A | AAG | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-2275_721-2274i others(4): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297584 | ||||||
chr12:4297586 | A | C | 144 | a0001c0001t0002g0239 a0001c0001t0003g0004 a0001c0001t0003g0006 others(141): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.721-2274A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297586 | |||||||
chr12:4297588 | A | AAAG | 5 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0077 others(2): Show |
8 | HG01109.hp1 HG01884.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-2270_721-2269i others(5): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4297588 | ||||||
chr12:4297588 | A | G | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-2272A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297588 | |||||||
chr12:4297592 | A | G | 20 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0077 others(17): Show |
28 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-2268A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297592 | |||||||
chr12:4297633 | G | C | 20 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0077 others(17): Show |
28 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-2227G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297633 | |||||||
chr12:4297670 | C | A | 137 | a0001c0001t0002g0029 a0001c0001t0002g0033 a0001c0001t0002g0035 others(134): Show |
151 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.721-2190C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297670 | |||||||
chr12:4297719 | G | A | 20 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0077 others(17): Show |
28 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-2141G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297719 | |||||||
chr12:4297721 | A | G | 20 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0077 others(17): Show |
28 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-2139A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297721 | |||||||
chr12:4297777 | A | G | 1 | a0001c0002t0065g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-2083A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297777 | |||||||
chr12:4297813 | C | A | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-2047C>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297813 | |||||||
chr12:4297895 | T | C | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1965T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4297895 | |||||||
chr12:4298000 | A | G | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1860A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298000 | |||||||
chr12:4298071 | G | C | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1789G>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298071 | |||||||
chr12:4298183 | G | A | 1 | a0001c0001t0024g0175 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.721-1677G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298183 | |||||||
chr12:4298237 | T | C | 3 | a0001c0001t0002g0152 a0001c0001t0002g0157 a0001c0001t0002g0342 |
3 | HG01978.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.721-1623T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298237 | |||||||
chr12:4298294 | T | C | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1566T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298294 | |||||||
chr12:4298416 | A | C | 1 | a0001c0001t0014g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.721-1444A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298416 | |||||||
chr12:4298464 | T | G | 17 | a0001c0001t0007g0001 a0001c0001t0007g0290 a0001c0001t0007g0311 others(14): Show |
24 | HG01928.hp1 HG01928.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.721-1396T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298464 | |||||||
chr12:4298466 | T | G | 49 | a0001c0001t0002g0029 a0001c0001t0002g0033 a0001c0001t0002g0035 others(46): Show |
55 | HG00609.hp1 HG00741.hp2 HG01257.hp1 others(52): Show |
intron_variant | MODIFIER | c.721-1394T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298466 | |||||||
chr12:4298725 | G | A | 1 | a0001c0002t0009g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.721-1135G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298725 | |||||||
chr12:4298815 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.721-1045G>A | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298815 | |||||||
chr12:4298826 | A | G | 1 | a0001c0001t0003g0355 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.721-1034A>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298826 | |||||||
chr12:4298862 | T | C | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-998T>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4298862 | |||||||
chr12:4299058 | A | AT | 81 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(78): Show |
94 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.721-791dupT | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4299058 | ||||||
chr12:4299058 | A | ATT | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-792_721-791dup others(2): Show |
CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 4299058 | ||||||
chr12:4299065 | T | G | 1 | a0001c0001t0083g0344 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.721-795T>G | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4299065 | |||||||
chr12:4299507 | C | T | 219 | a0001c0001t0002g0029 a0001c0001t0002g0033 a0001c0001t0002g0035 others(216): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.721-353C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4299507 | |||||||
chr12:4299541 | A | T | 3 | a0001c0001t0010g0065 a0001c0001t0059g0066 a0001c0001t0086g0336 |
3 | HG01358.hp1 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-319A>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4299541 | |||||||
chr12:4299750 | A | C | 15 | a0001c0001t0011g0002 a0001c0001t0011g0034 a0001c0001t0011g0160 others(12): Show |
20 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-110A>C | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4299750 | |||||||
chr12:4299751 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0006g0024 a0001c0001t0006g0077 others(2): Show |
8 | HG01109.hp1 HG01884.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-109C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4299751 | |||||||
chr12:4299799 | C | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0327 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.721-61C>T | CCND2 | ENSG00000118971.9 | transcript | ENST00000261254.8 | protein_coding | 4/4 | chr12 | 4299799 |