Item | Value |
---|---|
geneid | 10297 |
ensemblid | ENSG00000115266.12 |
hgncid | 24036 |
symbol | APC2 |
name | APC regulator of WNT signaling pathway 2 |
refseq_nuc | NM_005883.3 |
refseq_prot | NP_005874.1 |
ensembl_nuc | ENST00000590469.6 |
ensembl_prot | ENSP00000467073.2 |
mane_status | MANE Select |
chr | chr19 |
start | 1450121 |
end | 1473244 |
strand | + |
ver | v1.2 |
region | chr19:1450121-1473244 |
region5000 | chr19:1445121-1478244 |
regionname0 | APC2_chr19_1450121_1473244 |
regionname5000 | APC2_chr19_1445121_1478244 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2303 | 259 | 31 | 68 | 110 | 13 | 35 | 75 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0002 | 0/0 | 2303 | 18 | 15 | 0 | 1 | 1 | 1 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0003 | 0/0 | 2303 | 17 | 12 | 3 | 0 | 0 | 2 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0004 | 0/0 | 2303 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0005 | 0/0 | 2303 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0006 | 0/0 | 2303 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0007 | 0/0 | 2303 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0008 | 0/0 | 2303 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0009 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0010 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0011 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0012 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0013 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0014 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0015 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0016 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0017 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0018 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0019 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0020 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0021 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0022 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0023 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0024 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0025 | 0/0 | 2295 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2290): Show |
chr19 | 1445121 | 1478244 |
a0026 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0027 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0028 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0029 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0030 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0031 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0032 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
a0033 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | MASSV others(2298): Show |
chr19 | 1445121 | 1478244 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 6909 | 207 | 26 | 54 | 84 | 12 | 31 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0003 | 0/0 | 6909 | 14 | 0 | 0 | 13 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0005 | 1/0 | 6909 | 9 | 1 | 4 | 0 | 1 | 2 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0008 | 0/1 | 6909 | 5 | 0 | 3 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0013 | 0/0 | 6909 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0016 | 0/0 | 6909 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0019 | 0/0 | 6909 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0020 | 0/0 | 6909 | 2 | 1 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0022 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0023 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0028 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0030 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0031 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0032 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0033 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0036 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0038 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0039 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0041 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0046 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0053 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0056 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0059 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0001c0062 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0002c0002 | 0/0 | 6909 | 18 | 15 | 0 | 1 | 1 | 1 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0003c0006 | 0/0 | 6909 | 6 | 1 | 3 | 0 | 0 | 2 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0003c0007 | 0/0 | 6909 | 6 | 6 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0003c0015 | 0/0 | 6909 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0003c0017 | 0/0 | 6909 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0003c0061 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0004c0009 | 0/0 | 6909 | 4 | 3 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0004c0010 | 0/0 | 6909 | 4 | 4 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0004c0011 | 0/0 | 6909 | 4 | 4 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0004c0047 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0005c0004 | 0/0 | 6909 | 9 | 9 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0005c0014 | 0/0 | 6909 | 2 | 1 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0005c0060 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0006c0012 | 0/0 | 6909 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0007c0021 | 0/0 | 6909 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0008c0018 | 0/0 | 6909 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0009c0043 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0010c0037 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0011c0048 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0012c0027 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0013c0065 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0014c0058 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0015c0057 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0016c0064 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0017c0051 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0018c0045 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0019c0035 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0020c0029 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0021c0044 | 0/0 | 6909 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0022c0054 | 0/0 | 6909 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0023c0063 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0024c0034 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0025c0049 | 0/0 | 6885 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6880): Show |
chr19 | 1445121 | 1478244 | ||
a0026c0055 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0027c0042 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0028c0040 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0029c0026 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0030c0052 | 0/0 | 6909 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0031c0050 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0032c0024 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 | ||
a0033c0025 | 0/0 | 6909 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | ATGGC others(6904): Show |
chr19 | 1445121 | 1478244 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10179 | 165 | 14 | 45 | 66 | 11 | 29 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0005 | 0/0 | 10179 | 6 | 0 | 0 | 6 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0007 | 0/0 | 10179 | 5 | 5 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0008 | 0/0 | 10179 | 4 | 0 | 4 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0009 | 0/0 | 10179 | 4 | 0 | 3 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0010 | 0/0 | 10179 | 3 | 0 | 0 | 3 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0014 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0015 | 0/0 | 10179 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0016 | 0/0 | 10179 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0017 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0018 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0022 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0024 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0026 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0027 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0028 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0029 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0032 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0033 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0035 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0036 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0037 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0001t0038 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0003t0001 | 0/0 | 10179 | 11 | 0 | 0 | 10 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0003t0014 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0003t0025 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0003t0034 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0005t0001 | 1/0 | 10179 | 8 | 1 | 3 | 0 | 1 | 2 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0005t0043 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0008t0001 | 0/1 | 10179 | 5 | 0 | 3 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0013t0001 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0016t0001 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0019t0001 | 0/0 | 10179 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0020t0001 | 0/0 | 10179 | 2 | 1 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0022t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0023t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0028t0005 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0030t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0031t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0032t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0033t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0036t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0038t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0039t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0041t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0046t0023 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0053t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0056t0001 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0059t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0001c0062t0030 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0002c0002t0002 | 0/0 | 10179 | 15 | 12 | 0 | 1 | 1 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0002c0002t0044 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0002c0002t0048 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0002c0002t0049 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0006t0011 | 0/0 | 10179 | 3 | 0 | 2 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0006t0013 | 0/0 | 10179 | 2 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0006t0047 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0007t0006 | 0/0 | 10179 | 6 | 6 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0015t0012 | 0/0 | 10179 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0017t0045 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0017t0046 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0003c0061t0012 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0009t0004 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0009t0019 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0009t0040 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0009t0041 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0010t0004 | 0/0 | 10179 | 3 | 3 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0010t0019 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0011t0004 | 0/0 | 10179 | 4 | 4 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0004c0047t0042 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0005c0004t0003 | 0/0 | 10173 | 9 | 9 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10168): Show |
chr19 | 1445121 | 1478244 |
a0005c0014t0003 | 0/0 | 10173 | 2 | 1 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10168): Show |
chr19 | 1445121 | 1478244 |
a0005c0060t0021 | 0/0 | 10173 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10168): Show |
chr19 | 1445121 | 1478244 |
a0006c0012t0001 | 0/0 | 10179 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0007c0021t0001 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0008c0018t0001 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0009c0043t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0010c0037t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0011c0048t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0012c0027t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0013c0065t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0014c0058t0020 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0015c0057t0001 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0016c0064t0004 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0017c0051t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0018c0045t0001 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0019c0035t0002 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0020c0029t0003 | 0/0 | 10173 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10168): Show |
chr19 | 1445121 | 1478244 |
a0021c0044t0001 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0022c0054t0001 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0023c0063t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0024c0034t0001 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0025c0049t0010 | 0/0 | 10155 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10150): Show |
chr19 | 1445121 | 1478244 |
a0026c0055t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0027c0042t0018 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0028c0040t0001 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0029c0026t0002 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0030c0052t0031 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0031c0050t0001 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0032c0024t0008 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
a0033c0025t0039 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | GCGGT others(10174): Show |
chr19 | 1445121 | 1478244 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 6 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 3 | 1 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0007g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0008g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0009g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0015g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0017g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0017g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0018g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0022g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0024g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0026g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0027g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0028g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0029g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0032g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0033g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0035g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0036g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0037g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0001t0038g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0025g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0003t0034g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0005t0043g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0008t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0008t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0008t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0008t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0008t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0013t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0016t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0016t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0019t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0019t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0020t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0020t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0022t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0023t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0028t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0030t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0031t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0032t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0033t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0036t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0038t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0039t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0041t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0046t0023g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0053t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0056t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0059t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0001c0062t0030g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0044g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0048g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0002c0002t0049g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0006t0011g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0006t0011g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0006t0011g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0006t0013g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0006t0013g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0006t0047g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0007t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0007t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0007t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0007t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0007t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0007t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0015t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0015t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0017t0045g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0017t0046g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0003c0061t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0009t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0009t0019g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0009t0040g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0009t0041g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0010t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0010t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0010t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0010t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0011t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0011t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0011t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0004c0047t0042g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0004t0003g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0004t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0004t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0014t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0014t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0005c0060t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0006c0012t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0006c0012t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0007c0021t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0007c0021t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0008c0018t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0008c0018t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0009c0043t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0010c0037t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0011c0048t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0012c0027t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0013c0065t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0014c0058t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0015c0057t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0016c0064t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0017c0051t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0018c0045t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0019c0035t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0020c0029t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0021c0044t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0022c0054t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0023c0063t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0024c0034t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0025c0049t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0026c0055t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0027c0042t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0028c0040t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0029c0026t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0030c0052t0031g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0031c0050t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0032c0024t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
a0033c0025t0039g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00140 | hp1 | a0001 | c0005 | t0001 | g0003 | EUR | GBR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0078 | EUR | FIN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00544 | hp1 | a0009 | c0043 | t0001 | g0219 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00544 | hp2 | a0001 | c0001 | t0038 | g0043 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00558 | hp2 | a0001 | c0013 | t0001 | g0048 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00597 | hp2 | a0001 | c0039 | t0001 | g0216 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00609 | hp2 | a0001 | c0033 | t0001 | g0001 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00733 | hp1 | a0001 | c0001 | t0009 | g0242 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00733 | hp2 | a0010 | c0037 | t0001 | g0081 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00735 | hp1 | a0001 | c0059 | t0001 | g0132 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG00741 | hp2 | a0001 | c0001 | t0009 | g0077 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01074 | hp1 | a0001 | c0005 | t0043 | g0052 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01074 | hp2 | a0001 | c0001 | t0022 | g0101 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01081 | hp1 | a0001 | c0008 | t0001 | g0024 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01099 | hp1 | a0011 | c0048 | t0001 | g0070 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01106 | hp1 | a0001 | c0019 | t0001 | g0274 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01109 | hp1 | a0006 | c0012 | t0001 | g0002 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01109 | hp2 | a0005 | c0014 | t0003 | g0026 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01167 | hp2 | a0001 | c0001 | t0009 | g0037 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01175 | hp2 | a0001 | c0020 | t0001 | g0217 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01192 | hp1 | a0001 | c0001 | t0026 | g0262 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01192 | hp2 | a0004 | c0009 | t0019 | g0234 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01243 | hp1 | a0003 | c0006 | t0011 | g0203 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01243 | hp2 | a0001 | c0019 | t0001 | g0275 | AMR | PUR | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01255 | hp2 | a0003 | c0006 | t0011 | g0133 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01257 | hp2 | a0001 | c0008 | t0001 | g0109 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01258 | hp2 | a0001 | c0008 | t0001 | g0014 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01261 | hp1 | a0006 | c0012 | t0001 | g0084 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01346 | hp1 | a0012 | c0027 | t0001 | g0204 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01358 | hp1 | a0003 | c0006 | t0013 | g0245 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01884 | hp1 | a0005 | c0004 | t0003 | g0236 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01884 | hp2 | a0003 | c0007 | t0006 | g0265 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01891 | hp1 | a0002 | c0002 | t0049 | g0182 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01934 | hp1 | a0001 | c0022 | t0001 | g0003 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01943 | hp2 | a0001 | c0005 | t0001 | g0004 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01978 | hp2 | a0001 | c0032 | t0001 | g0158 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01993 | hp1 | a0013 | c0065 | t0001 | g0205 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02015 | hp2 | a0001 | c0001 | t0035 | g0183 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02040 | hp1 | a0001 | c0031 | t0001 | g0001 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02055 | hp1 | a0003 | c0007 | t0006 | g0032 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02083 | hp2 | a0001 | c0038 | t0001 | g0192 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02129 | hp2 | a0001 | c0001 | t0028 | g0137 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02145 | hp1 | a0001 | c0001 | t0016 | g0003 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0272 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02148 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CDX | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02257 | hp1 | a0005 | c0004 | t0003 | g0239 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02257 | hp2 | a0001 | c0001 | t0037 | g0269 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02258 | hp1 | a0014 | c0058 | t0020 | g0277 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0163 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02273 | hp1 | a0001 | c0005 | t0001 | g0004 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02273 | hp2 | a0001 | c0041 | t0001 | g0130 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02280 | hp2 | a0002 | c0002 | t0044 | g0281 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02293 | hp2 | a0015 | c0057 | t0001 | g0007 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02451 | hp1 | a0005 | c0004 | t0003 | g0168 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02523 | hp1 | a0017 | c0051 | t0001 | g0208 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02572 | hp1 | a0004 | c0009 | t0041 | g0231 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02572 | hp2 | a0001 | c0001 | t0027 | g0031 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02622 | hp1 | a0018 | c0045 | t0001 | g0050 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0238 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0267 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02630 | hp2 | a0003 | c0006 | t0047 | g0263 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02647 | hp1 | a0004 | c0010 | t0019 | g0055 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02647 | hp2 | a0004 | c0009 | t0040 | g0233 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02698 | hp1 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02698 | hp2 | a0003 | c0006 | t0013 | g0202 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02717 | hp2 | a0003 | c0015 | t0012 | g0165 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02723 | hp1 | a0005 | c0004 | t0003 | g0020 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02738 | hp1 | a0001 | c0005 | t0001 | g0053 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0144 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02886 | hp2 | a0004 | c0010 | t0004 | g0059 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02895 | hp1 | a0001 | c0062 | t0030 | g0151 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02922 | hp1 | a0001 | c0001 | t0016 | g0113 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02922 | hp2 | a0003 | c0007 | t0006 | g0256 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02965 | hp1 | a0004 | c0010 | t0004 | g0058 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02970 | hp1 | a0003 | c0007 | t0006 | g0258 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02970 | hp2 | a0001 | c0046 | t0023 | g0241 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02976 | hp1 | a0019 | c0035 | t0002 | g0068 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02976 | hp2 | a0004 | c0009 | t0004 | g0264 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03041 | hp1 | a0004 | c0010 | t0004 | g0061 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03041 | hp2 | a0005 | c0004 | t0003 | g0243 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03098 | hp1 | a0003 | c0017 | t0046 | g0171 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03130 | hp1 | a0004 | c0011 | t0004 | g0278 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03130 | hp2 | a0005 | c0060 | t0021 | g0060 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03139 | hp2 | a0005 | c0004 | t0003 | g0005 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0271 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03209 | hp1 | a0004 | c0011 | t0004 | g0279 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03225 | hp1 | a0003 | c0015 | t0012 | g0161 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0162 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0009 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03486 | hp2 | a0005 | c0004 | t0003 | g0005 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03516 | hp1 | a0003 | c0017 | t0045 | g0253 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03516 | hp2 | a0020 | c0029 | t0003 | g0020 | AFR | ESN | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03579 | hp1 | a0003 | c0007 | t0006 | g0257 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03579 | hp2 | a0001 | c0020 | t0001 | g0001 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03654 | hp2 | a0001 | c0008 | t0001 | g0023 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03688 | hp1 | a0003 | c0006 | t0011 | g0244 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03927 | hp2 | a0021 | c0044 | t0001 | g0188 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03942 | hp1 | a0001 | c0001 | t0036 | g0003 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03942 | hp2 | a0022 | c0054 | t0001 | g0016 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0003 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04199 | hp2 | a0001 | c0001 | t0024 | g0002 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18522 | hp1 | a0005 | c0004 | t0003 | g0005 | AFR | YRI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0009 | AFR | YRI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18747 | hp2 | a0023 | c0063 | t0001 | g0091 | EAS | CHB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18906 | hp1 | a0005 | c0004 | t0003 | g0005 | AFR | YRI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18906 | hp2 | a0024 | c0034 | t0001 | g0270 | AFR | YRI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18939 | hp1 | a0001 | c0028 | t0005 | g0185 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18941 | hp2 | a0001 | c0030 | t0001 | g0155 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18944 | hp1 | a0025 | c0049 | t0010 | g0003 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18945 | hp1 | a0001 | c0001 | t0014 | g0002 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18946 | hp1 | a0001 | c0001 | t0029 | g0218 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18947 | hp1 | a0026 | c0055 | t0001 | g0003 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18948 | hp1 | a0001 | c0013 | t0001 | g0001 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18952 | hp2 | a0001 | c0003 | t0025 | g0002 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18959 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18960 | hp1 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18960 | hp2 | a0007 | c0021 | t0001 | g0147 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18963 | hp2 | a0001 | c0016 | t0001 | g0117 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18965 | hp1 | a0008 | c0018 | t0001 | g0170 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0096 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18979 | hp2 | a0001 | c0016 | t0001 | g0015 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18984 | hp2 | a0027 | c0042 | t0018 | g0001 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18985 | hp1 | a0001 | c0003 | t0034 | g0025 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18990 | hp2 | a0001 | c0001 | t0033 | g0210 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18992 | hp1 | a0028 | c0040 | t0001 | g0092 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18995 | hp2 | a0001 | c0036 | t0001 | g0003 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18998 | hp1 | a0001 | c0001 | t0017 | g0108 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18999 | hp1 | a0001 | c0023 | t0001 | g0090 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA18999 | hp2 | a0029 | c0026 | t0002 | g0180 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19011 | hp1 | a0001 | c0003 | t0014 | g0003 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19012 | hp1 | a0008 | c0018 | t0001 | g0169 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19030 | hp1 | a0005 | c0014 | t0003 | g0250 | AFR | LWK | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19030 | hp2 | a0003 | c0061 | t0012 | g0056 | AFR | LWK | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | LWK | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19043 | hp2 | a0002 | c0002 | t0048 | g0173 | AFR | LWK | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19063 | hp2 | a0007 | c0021 | t0001 | g0148 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19074 | hp2 | a0001 | c0001 | t0018 | g0141 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19088 | hp2 | a0030 | c0052 | t0031 | g0194 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19090 | hp1 | a0001 | c0053 | t0001 | g0220 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19090 | hp2 | a0001 | c0001 | t0017 | g0120 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19240 | hp1 | a0001 | c0001 | t0032 | g0228 | AFR | YRI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA19240 | hp2 | a0031 | c0050 | t0001 | g0099 | AFR | YRI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0266 | EUR | TSI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | TSI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | GIH | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG01123 | hp2 | a0001 | c0005 | t0001 | g0153 | AMR | CLM | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02109 | hp1 | a0003 | c0007 | t0006 | g0028 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02486 | hp1 | a0004 | c0047 | t0042 | g0240 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02486 | hp2 | a0016 | c0064 | t0004 | g0057 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0159 | AFR | ACB | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03471 | hp1 | a0001 | c0056 | t0001 | g0229 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0268 | AFR | MSL | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG06807 | hp1 | a0004 | c0011 | t0004 | g0021 | AFR | USA | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
HG06807 | hp2 | a0001 | c0005 | t0001 | g0034 | AFR | USA | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20300 | hp1 | a0032 | c0024 | t0008 | g0103 | AFR | USA | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA20300 | hp2 | a0004 | c0011 | t0004 | g0021 | AFR | USA | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA21309 | hp1 | a0033 | c0025 | t0039 | g0139 | AFR | LWK | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0273 | AFR | LWK | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
homoSapiens | chm13v2 | a0001 | c0008 | t0001 | g0129 | REF | REF | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
homoSapiens | grch38p0 | a0001 | c0005 | t0001 | g0007 | REF | REF | APC2_chr19_1445121_1478244 | APC2 | chr19 | 1445121 | 1478244 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1453018 | C | T | 1 | a0013 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.17C>T | p.Ala6Val | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 2/15 | 253/10179 | 17/6912 | 6/2303 | chr19 | 1453018 | |||
chr19:1453522 | C | G | 1 | a0023 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.324C>G | p.Ser108Arg | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/15 | 560/10179 | 324/6912 | 108/2303 | chr19 | 1453522 | |||
chr19:1456952 | G | A | 1 | a0032 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.916G>A | p.Val306Met | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/15 | 1152/10179 | 916/6912 | 306/2303 | chr19 | 1456952 | |||
chr19:1457003 | G | C | 1 | a0006 | 2 | HG01109.hp1 HG01261.hp1 |
missense_variant | MODERATE | c.967G>C | p.Gly323Arg | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/15 | 1203/10179 | 967/6912 | 323/2303 | chr19 | 1457003 | |||
chr19:1457072 | C | T | 1 | a0014 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1036C>T | p.Arg346Cys | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/15 | 1272/10179 | 1036/6912 | 346/2303 | chr19 | 1457072 | |||
chr19:1458043 | G | A | 1 | a0016 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1286G>A | p.Arg429His | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/15 | 1522/10179 | 1286/6912 | 429/2303 | chr19 | 1458043 | |||
chr19:1460241 | G | A | 1 | a0033 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1364G>A | p.Arg455Gln | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/15 | 1600/10179 | 1364/6912 | 455/2303 | chr19 | 1460241 | |||
chr19:1460309 | G | A | 1 | a0029 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1432G>A | p.Val478Ile | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/15 | 1668/10179 | 1432/6912 | 478/2303 | chr19 | 1460309 | |||
chr19:1460801 | G | T | 1 | a0015 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1465G>T | p.Gly489Cys | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/15 | 1701/10179 | 1465/6912 | 489/2303 | chr19 | 1460801 | |||
chr19:1461143 | G | A | 1 | a0012 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1628G>A | p.Arg543Gln | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/15 | 1864/10179 | 1628/6912 | 543/2303 | chr19 | 1461143 | |||
chr19:1462059 | G | C | 1 | a0020 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1735G>C | p.Gly579Arg | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/15 | 1971/10179 | 1735/6912 | 579/2303 | chr19 | 1462059 | |||
chr19:1465787 | C | T | 1 | a0026 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.2486C>T | p.Ala829Val | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2722/10179 | 2486/6912 | 829/2303 | chr19 | 1465787 | |||
chr19:1466024 | G | T | 1 | a0022 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2723G>T | p.Arg908Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2959/10179 | 2723/6912 | 908/2303 | chr19 | 1466024 | |||
chr19:1466146 | G | A | 2 | a0005 a0020 |
13 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.2845G>A | p.Ala949Thr | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 3081/10179 | 2845/6912 | 949/2303 | chr19 | 1466146 | |||
chr19:1466230 | G | A | 1 | a0024 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.2929G>A | p.Glu977Lys | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 3165/10179 | 2929/6912 | 977/2303 | chr19 | 1466230 | |||
chr19:1467214 | G | A | 1 | a0010 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.3913G>A | p.Gly1305Ser | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4149/10179 | 3913/6912 | 1305/2303 | chr19 | 1467214 | |||
chr19:1467668 | G | C | 3 | a0002 a0019 a0029 |
20 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(17): Show |
missense_variant | MODERATE | c.4367G>C | p.Arg1456Pro | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4603/10179 | 4367/6912 | 1456/2303 | chr19 | 1467668 | |||
chr19:1467712 | C | T | 1 | a0029 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.4411C>T | p.Arg1471Trp | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4647/10179 | 4411/6912 | 1471/2303 | chr19 | 1467712 | |||
chr19:1467884 | G | A | 1 | a0008 | 2 | NA18965.hp1 NA19012.hp1 |
missense_variant | MODERATE | c.4583G>A | p.Arg1528Gln | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4819/10179 | 4583/6912 | 1528/2303 | chr19 | 1467884 | |||
chr19:1467932 | G | A | 1 | a0019 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.4631G>A | p.Gly1544Asp | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4867/10179 | 4631/6912 | 1544/2303 | chr19 | 1467932 | |||
chr19:1468082 | C | T | 1 | a0030 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.4781C>T | p.Pro1594Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5017/10179 | 4781/6912 | 1594/2303 | chr19 | 1468082 | |||
chr19:1468247 | G | A | 1 | a0033 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.4946G>A | p.Arg1649His | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5182/10179 | 4946/6912 | 1649/2303 | chr19 | 1468247 | |||
chr19:1468267 | C | G | 1 | a0017 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.4966C>G | p.Arg1656Gly | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5202/10179 | 4966/6912 | 1656/2303 | chr19 | 1468267 | |||
chr19:1468697 | C | T | 1 | a0031 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.5396C>T | p.Pro1799Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5632/10179 | 5396/6912 | 1799/2303 | chr19 | 1468697 | |||
chr19:1468799 | CGAGCCCC others(17): Show |
C | 1 | a0025 | 1 | NA18944.hp1 | disruptive_inframe_deletion | MODERATE | c.5504_5527delCCGGGC others(18): Show |
p.Pro1835_Ser1842del | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5740/10179 | 5504/6912 | 1835/2303 | INFO_REALIGN_3_PRIME | chr19 | 1468799 | ||
chr19:1468802 | G | A | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.5501G>A | p.Ser1834Asn | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5737/10179 | 5501/6912 | 1834/2303 | chr19 | 1468802 | |||
chr19:1468897 | G | C | 1 | a0028 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.5596G>C | p.Ala1866Pro | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5832/10179 | 5596/6912 | 1866/2303 | chr19 | 1468897 | |||
chr19:1468913 | C | T | 1 | a0011 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.5612C>T | p.Thr1871Ile | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5848/10179 | 5612/6912 | 1871/2303 | chr19 | 1468913 | |||
chr19:1469224 | G | A | 1 | a0027 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.5923G>A | p.Val1975Met | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6159/10179 | 5923/6912 | 1975/2303 | chr19 | 1469224 | |||
chr19:1469372 | C | T | 2 | a0004 a0016 |
14 | HG01192.hp2 HG02486.hp1 HG02486.hp2 others(11): Show |
missense_variant | MODERATE | c.6071C>T | p.Ala2024Val | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6307/10179 | 6071/6912 | 2024/2303 | chr19 | 1469372 | |||
chr19:1469380 | C | A | 1 | a0009 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.6079C>A | p.Arg2027Ser | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6315/10179 | 6079/6912 | 2027/2303 | chr19 | 1469380 | |||
chr19:1469468 | C | A | 1 | a0021 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.6167C>A | p.Pro2056Gln | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6403/10179 | 6167/6912 | 2056/2303 | chr19 | 1469468 | |||
chr19:1469470 | G | A | 3 | a0002 a0019 a0029 |
20 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(17): Show |
missense_variant | MODERATE | c.6169G>A | p.Ala2057Thr | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6405/10179 | 6169/6912 | 2057/2303 | chr19 | 1469470 | |||
chr19:1469531 | C | G | 10 | a0002 a0003 a0004 others(7): Show |
66 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(63): Show |
missense_variant | MODERATE | c.6230C>G | p.Thr2077Ser | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6466/10179 | 6230/6912 | 2077/2303 | chr19 | 1469531 | |||
chr19:1469543 | C | T | 1 | a0007 | 2 | NA18960.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.6242C>T | p.Pro2081Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6478/10179 | 6242/6912 | 2081/2303 | chr19 | 1469543 | |||
chr19:1469834 | C | T | 1 | a0018 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.6533C>T | p.Pro2178Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6769/10179 | 6533/6912 | 2178/2303 | chr19 | 1469834 | |||
chr19:1470022 | T | G | 2 | a0004 a0016 |
14 | HG01192.hp2 HG02486.hp1 HG02486.hp2 others(11): Show |
missense_variant | MODERATE | c.6721T>G | p.Ser2241Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6957/10179 | 6721/6912 | 2241/2303 | chr19 | 1470022 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1453309 | G | A | 3 | a0001c0003 a0001c0022 a0001c0023 |
16 | HG00408.hp1 HG00673.hp1 HG01934.hp1 others(13): Show |
synonymous_variant | LOW | c.204G>A | p.Gly68Gly | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 3/15 | 440/10179 | 204/6912 | 68/2303 | chr19 | 1453309 | |||
chr19:1453454 | C | T | 1 | a0004c0011 | 4 | HG03130.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
synonymous_variant | LOW | c.256C>T | p.Leu86Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/15 | 492/10179 | 256/6912 | 86/2303 | chr19 | 1453454 | |||
chr19:1453519 | C | T | 1 | a0016c0064 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.321C>T | p.Gly107Gly | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/15 | 557/10179 | 321/6912 | 107/2303 | chr19 | 1453519 | |||
chr19:1456115 | C | T | 5 | a0001c0062 a0003c0061 a0004c0010 others(2): Show |
8 | HG02486.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
synonymous_variant | LOW | c.679C>T | p.Leu227Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 7/15 | 915/10179 | 679/6912 | 227/2303 | chr19 | 1456115 | |||
chr19:1456951 | C | T | 1 | a0001c0059 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.915C>T | p.Cys305Cys | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/15 | 1151/10179 | 915/6912 | 305/2303 | chr19 | 1456951 | |||
chr19:1460194 | C | T | 1 | a0001c0008 | 4 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
synonymous_variant | LOW | c.1317C>T | p.Ala439Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/15 | 1553/10179 | 1317/6912 | 439/2303 | chr19 | 1460194 | |||
chr19:1460815 | C | T | 1 | a0001c0056 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1479C>T | p.Ala493Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/15 | 1715/10179 | 1479/6912 | 493/2303 | chr19 | 1460815 | |||
chr19:1460836 | C | T | 1 | a0003c0007 | 6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
synonymous_variant | LOW | c.1500C>T | p.Ser500Ser | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/15 | 1736/10179 | 1500/6912 | 500/2303 | chr19 | 1460836 | |||
chr19:1461126 | G | A | 1 | a0001c0013 | 2 | HG00558.hp2 NA18948.hp1 |
synonymous_variant | LOW | c.1611G>A | p.Leu537Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/15 | 1847/10179 | 1611/6912 | 537/2303 | chr19 | 1461126 | |||
chr19:1461995 | G | A | 1 | a0001c0028 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.1671G>A | p.Leu557Leu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/15 | 1907/10179 | 1671/6912 | 557/2303 | chr19 | 1461995 | |||
chr19:1465365 | C | A | 1 | a0001c0030 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2064C>A | p.Ala688Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2300/10179 | 2064/6912 | 688/2303 | chr19 | 1465365 | |||
chr19:1465821 | G | A | 1 | a0001c0031 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.2520G>A | p.Ala840Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2756/10179 | 2520/6912 | 840/2303 | chr19 | 1465821 | |||
chr19:1465869 | G | A | 1 | a0001c0032 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.2568G>A | p.Gln856Gln | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2804/10179 | 2568/6912 | 856/2303 | chr19 | 1465869 | |||
chr19:1466028 | G | A | 1 | a0001c0033 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.2727G>A | p.Ala909Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2963/10179 | 2727/6912 | 909/2303 | chr19 | 1466028 | |||
chr19:1466253 | C | A | 9 | a0002c0002 a0003c0007 a0003c0015 others(6): Show |
40 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(37): Show |
synonymous_variant | LOW | c.2952C>A | p.Thr984Thr | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 3188/10179 | 2952/6912 | 984/2303 | chr19 | 1466253 | |||
chr19:1466421 | C | T | 1 | a0001c0053 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.3120C>T | p.Pro1040Pro | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 3356/10179 | 3120/6912 | 1040/2303 | chr19 | 1466421 | |||
chr19:1466698 | C | A | 1 | a0001c0036 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.3397C>A | p.Arg1133Arg | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 3633/10179 | 3397/6912 | 1133/2303 | chr19 | 1466698 | |||
chr19:1467279 | G | A | 4 | a0005c0004 a0005c0014 a0005c0060 others(1): Show |
13 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
synonymous_variant | LOW | c.3978G>A | p.Ala1326Ala | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4214/10179 | 3978/6912 | 1326/2303 | chr19 | 1467279 | |||
chr19:1467447 | G | A | 1 | a0001c0016 | 2 | NA18963.hp2 NA18979.hp2 |
synonymous_variant | LOW | c.4146G>A | p.Pro1382Pro | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4382/10179 | 4146/6912 | 1382/2303 | chr19 | 1467447 | |||
chr19:1467456 | G | A | 1 | a0001c0038 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.4155G>A | p.Glu1385Glu | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4391/10179 | 4155/6912 | 1385/2303 | chr19 | 1467456 | |||
chr19:1467561 | G | C | 3 | a0003c0007 a0003c0015 a0003c0061 |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
synonymous_variant | LOW | c.4260G>C | p.Gly1420Gly | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4496/10179 | 4260/6912 | 1420/2303 | chr19 | 1467561 | |||
chr19:1467685 | A | C | 62 | a0001c0001 a0001c0003 a0001c0008 others(59): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
synonymous_variant | LOW | c.4384A>C | p.Arg1462Arg | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4620/10179 | 4384/6912 | 1462/2303 | chr19 | 1467685 | |||
chr19:1467771 | C | T | 4 | a0004c0009 a0004c0010 a0004c0011 others(1): Show |
13 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
synonymous_variant | LOW | c.4470C>T | p.Asp1490Asp | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4706/10179 | 4470/6912 | 1490/2303 | chr19 | 1467771 | |||
chr19:1467774 | G | A | 1 | a0003c0017 | 2 | HG03098.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.4473G>A | p.Gly1491Gly | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4709/10179 | 4473/6912 | 1491/2303 | chr19 | 1467774 | |||
chr19:1467804 | C | T | 2 | a0003c0006 a0014c0058 |
7 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(4): Show |
synonymous_variant | LOW | c.4503C>T | p.Pro1501Pro | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 4739/10179 | 4503/6912 | 1501/2303 | chr19 | 1467804 | |||
chr19:1468122 | C | A | 1 | a0001c0039 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.4821C>A | p.Thr1607Thr | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5057/10179 | 4821/6912 | 1607/2303 | chr19 | 1468122 | |||
chr19:1468329 | C | T | 4 | a0004c0009 a0004c0010 a0004c0011 others(1): Show |
13 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
synonymous_variant | LOW | c.5028C>T | p.Asp1676Asp | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5264/10179 | 5028/6912 | 1676/2303 | chr19 | 1468329 | |||
chr19:1468458 | C | T | 1 | a0001c0023 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.5157C>T | p.Ser1719Ser | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5393/10179 | 5157/6912 | 1719/2303 | chr19 | 1468458 | |||
chr19:1469031 | A | G | 20 | a0001c0046 a0002c0002 a0003c0006 others(17): Show |
67 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(64): Show |
synonymous_variant | LOW | c.5730A>G | p.Lys1910Lys | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5966/10179 | 5730/6912 | 1910/2303 | chr19 | 1469031 | |||
chr19:1469034 | G | A | 1 | a0001c0041 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.5733G>A | p.Thr1911Thr | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 5969/10179 | 5733/6912 | 1911/2303 | chr19 | 1469034 | |||
chr19:1469079 | G | A | 4 | a0005c0004 a0005c0014 a0005c0060 others(1): Show |
13 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
synonymous_variant | LOW | c.5778G>A | p.Ser1926Ser | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6014/10179 | 5778/6912 | 1926/2303 | chr19 | 1469079 | |||
chr19:1469094 | G | A | 2 | a0003c0015 a0003c0061 |
3 | HG02717.hp2 HG03225.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.5793G>A | p.Pro1931Pro | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6029/10179 | 5793/6912 | 1931/2303 | chr19 | 1469094 | |||
chr19:1469820 | G | C | 1 | a0001c0019 | 2 | HG01106.hp1 HG01243.hp2 |
synonymous_variant | LOW | c.6519G>C | p.Thr2173Thr | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6755/10179 | 6519/6912 | 2173/2303 | chr19 | 1469820 | |||
chr19:1469889 | C | A | 1 | a0001c0020 | 2 | HG01175.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.6588C>A | p.Val2196Val | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 6824/10179 | 6588/6912 | 2196/2303 | chr19 | 1469889 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1450262 | G | T | 2 | a0001c0001t0008 a0032c0024t0008 |
5 | HG01069.hp2 HG01071.hp2 HG01928.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/15 | chr19 | 1450262 | |||||||
chr19:1470499 | G | T | 9 | a0002c0002t0002 a0002c0002t0044 a0002c0002t0048 others(6): Show |
23 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*286G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 286 | chr19 | 1470499 | ||||||
chr19:1470547 | G | A | 3 | a0003c0006t0011 a0003c0006t0013 a0014c0058t0020 |
6 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*334G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 334 | chr19 | 1470547 | ||||||
chr19:1470562 | CGGGTCT | C | 4 | a0005c0004t0003 a0005c0014t0003 a0005c0060t0021 others(1): Show |
13 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*361_*366delTGGGTC | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 361 | INFO_REALIGN_3_PRIME | chr19 | 1470562 | |||||
chr19:1470751 | G | A | 1 | a0001c0001t0022 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 538 | chr19 | 1470751 | ||||||
chr19:1470793 | G | C | 1 | a0001c0046t0023 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 580 | chr19 | 1470793 | ||||||
chr19:1470899 | G | A | 1 | a0002c0002t0044 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 686 | chr19 | 1470899 | ||||||
chr19:1470957 | G | T | 2 | a0003c0015t0012 a0003c0061t0012 |
3 | HG02717.hp2 HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*744G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 744 | chr19 | 1470957 | ||||||
chr19:1470989 | G | A | 1 | a0001c0001t0024 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 776 | chr19 | 1470989 | ||||||
chr19:1471006 | G | A | 1 | a0001c0003t0025 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*793G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 793 | chr19 | 1471006 | ||||||
chr19:1471070 | A | G | 1 | a0001c0005t0043 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*857A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 857 | chr19 | 1471070 | ||||||
chr19:1471072 | C | A | 2 | a0001c0001t0014 a0001c0003t0014 |
2 | NA18945.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*859C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 859 | chr19 | 1471072 | ||||||
chr19:1471128 | C | G | 24 | a0002c0002t0002 a0002c0002t0044 a0002c0002t0048 others(21): Show |
52 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*915C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 915 | chr19 | 1471128 | ||||||
chr19:1471167 | T | C | 5 | a0001c0001t0026 a0005c0004t0003 a0005c0014t0003 others(2): Show |
14 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*954T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 954 | chr19 | 1471167 | ||||||
chr19:1471268 | C | T | 1 | a0033c0025t0039 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1055 | chr19 | 1471268 | ||||||
chr19:1471360 | G | A | 3 | a0003c0006t0047 a0003c0017t0045 a0003c0017t0046 |
3 | HG02630.hp2 HG03098.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1147G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1147 | chr19 | 1471360 | ||||||
chr19:1471399 | G | C | 1 | a0001c0001t0009 | 4 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1186G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1186 | chr19 | 1471399 | ||||||
chr19:1471416 | A | G | 1 | a0004c0047t0042 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1203A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1203 | chr19 | 1471416 | ||||||
chr19:1471427 | T | C | 1 | a0002c0002t0048 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1214 | chr19 | 1471427 | ||||||
chr19:1471457 | C | T | 1 | a0001c0001t0038 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1244C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1244 | chr19 | 1471457 | ||||||
chr19:1471564 | T | C | 1 | a0003c0017t0045 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1351T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1351 | chr19 | 1471564 | ||||||
chr19:1471618 | G | A | 3 | a0003c0006t0011 a0003c0006t0013 a0014c0058t0020 |
6 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1405G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1405 | chr19 | 1471618 | ||||||
chr19:1471751 | G | A | 9 | a0004c0009t0004 a0004c0009t0019 a0004c0009t0040 others(6): Show |
14 | HG01192.hp2 HG02486.hp1 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1538G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1538 | chr19 | 1471751 | ||||||
chr19:1471844 | A | G | 1 | a0001c0001t0037 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1631A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1631 | chr19 | 1471844 | ||||||
chr19:1472008 | T | C | 34 | a0001c0001t0015 a0001c0001t0026 a0001c0001t0027 others(31): Show |
72 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1795T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1795 | chr19 | 1472008 | ||||||
chr19:1472077 | T | C | 1 | a0001c0001t0016 | 2 | HG02145.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1864T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1864 | chr19 | 1472077 | ||||||
chr19:1472191 | C | T | 1 | a0001c0001t0036 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1978C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 1978 | chr19 | 1472191 | ||||||
chr19:1472328 | G | A | 1 | a0001c0001t0028 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2115G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2115 | chr19 | 1472328 | ||||||
chr19:1472331 | G | A | 1 | a0001c0001t0029 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2118 | chr19 | 1472331 | ||||||
chr19:1472401 | C | T | 2 | a0001c0001t0010 a0025c0049t0010 |
4 | NA18942.hp1 NA18944.hp1 NA18959.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2188C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2188 | chr19 | 1472401 | ||||||
chr19:1472428 | C | T | 2 | a0001c0001t0018 a0027c0042t0018 |
2 | NA18984.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2215C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2215 | chr19 | 1472428 | ||||||
chr19:1472433 | T | C | 2 | a0003c0015t0012 a0003c0061t0012 |
3 | HG02717.hp2 HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2220T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2220 | chr19 | 1472433 | ||||||
chr19:1472555 | C | G | 1 | a0001c0001t0035 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2342C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2342 | chr19 | 1472555 | ||||||
chr19:1472568 | C | T | 1 | a0001c0003t0034 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2355C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2355 | chr19 | 1472568 | ||||||
chr19:1472574 | A | G | 3 | a0003c0006t0011 a0003c0006t0013 a0014c0058t0020 |
6 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2361A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2361 | chr19 | 1472574 | ||||||
chr19:1472593 | C | T | 1 | a0001c0001t0017 | 2 | NA18998.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2380C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2380 | chr19 | 1472593 | ||||||
chr19:1472719 | A | G | 1 | a0001c0001t0033 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2506A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2506 | chr19 | 1472719 | ||||||
chr19:1472736 | C | T | 13 | a0003c0006t0011 a0003c0006t0013 a0003c0006t0047 others(10): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2523C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2523 | chr19 | 1472736 | ||||||
chr19:1472753 | C | A | 2 | a0003c0015t0012 a0003c0061t0012 |
3 | HG02717.hp2 HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2540C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2540 | chr19 | 1472753 | ||||||
chr19:1472765 | G | A | 1 | a0001c0062t0030 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2552 | chr19 | 1472765 | ||||||
chr19:1472816 | C | T | 10 | a0003c0006t0047 a0004c0009t0004 a0004c0009t0019 others(7): Show |
15 | HG01192.hp2 HG02258.hp1 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2603C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2603 | chr19 | 1472816 | ||||||
chr19:1472826 | C | A | 1 | a0002c0002t0044 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2613C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2613 | chr19 | 1472826 | ||||||
chr19:1472920 | C | A | 2 | a0003c0015t0012 a0003c0061t0012 |
3 | HG02717.hp2 HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2707C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2707 | chr19 | 1472920 | ||||||
chr19:1472949 | A | G | 1 | a0001c0001t0032 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2736A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2736 | chr19 | 1472949 | ||||||
chr19:1472960 | C | T | 2 | a0001c0001t0005 a0001c0028t0005 |
7 | HG02129.hp1 HG02155.hp2 NA18939.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2747C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2747 | chr19 | 1472960 | ||||||
chr19:1472981 | C | G | 1 | a0001c0001t0037 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2768C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2768 | chr19 | 1472981 | ||||||
chr19:1473045 | C | T | 1 | a0003c0006t0013 | 2 | HG01358.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2832C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2832 | chr19 | 1473045 | ||||||
chr19:1473094 | C | T | 1 | a0030c0052t0031 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2881C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2881 | chr19 | 1473094 | ||||||
chr19:1473151 | C | T | 1 | a0002c0002t0049 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2938C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2938 | chr19 | 1473151 | ||||||
chr19:1473153 | T | C | 6 | a0001c0001t0007 a0001c0001t0027 a0001c0046t0023 others(3): Show |
10 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2940T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2940 | chr19 | 1473153 | ||||||
chr19:1473197 | C | G | 5 | a0002c0002t0044 a0004c0009t0004 a0004c0010t0004 others(2): Show |
10 | HG02280.hp2 HG02486.hp2 HG02886.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 15/15 | 2984 | chr19 | 1473197 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:1450404 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(130): Show |
151 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-19+66G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1450404 | |||||||
chr19:1450466 | A | C | 1 | a0002c0002t0044g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-19+128A>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1450466 | |||||||
chr19:1450513 | G | C | 3 | a0001c0001t0001g0022 a0001c0008t0001g0023 a0001c0008t0001g0024 |
3 | HG01081.hp1 HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-19+175G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1450513 | |||||||
chr19:1450874 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-19+536G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1450874 | |||||||
chr19:1450962 | G | A | 1 | a0005c0004t0003g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19+624G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1450962 | |||||||
chr19:1451134 | G | C | 2 | a0008c0018t0001g0169 a0008c0018t0001g0170 |
2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-19+796G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451134 | |||||||
chr19:1451171 | G | A | 3 | a0001c0001t0001g0172 a0002c0002t0048g0173 a0003c0017t0046g0171 |
3 | HG03098.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+833G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451171 | |||||||
chr19:1451196 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-19+858T>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451196 | |||||||
chr19:1451231 | G | C | 1 | a0001c0001t0015g0009 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-19+893G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451231 | |||||||
chr19:1451235 | A | T | 5 | a0001c0001t0001g0280 a0004c0011t0004g0021 a0004c0011t0004g0278 others(2): Show |
6 | HG02258.hp1 HG02280.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+897A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451235 | |||||||
chr19:1451241 | C | T | 5 | a0001c0001t0001g0280 a0004c0011t0004g0021 a0004c0011t0004g0278 others(2): Show |
6 | HG02258.hp1 HG02280.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+903C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451241 | |||||||
chr19:1451255 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(121): Show |
142 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+917C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451255 | |||||||
chr19:1451271 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(128): Show |
149 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-19+933A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451271 | |||||||
chr19:1451275 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(127): Show |
148 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-19+937C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451275 | |||||||
chr19:1451357 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-19+1019A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451357 | |||||||
chr19:1451401 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(126): Show |
147 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-19+1063C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451401 | |||||||
chr19:1451415 | C | T | 2 | a0001c0001t0001g0016 a0022c0054t0001g0016 |
2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-19+1077C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451415 | |||||||
chr19:1451448 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(120): Show |
140 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+1110T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451448 | |||||||
chr19:1451449 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(62): Show |
79 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-19+1111G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451449 | |||||||
chr19:1451463 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-19+1125C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451463 | |||||||
chr19:1451471 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-19+1133A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451471 | |||||||
chr19:1451659 | G | T | 7 | a0001c0001t0001g0172 a0001c0019t0001g0274 a0001c0019t0001g0275 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+1321G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451659 | |||||||
chr19:1451743 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(111): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.-18-1241G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451743 | |||||||
chr19:1451773 | C | T | 5 | a0001c0001t0001g0280 a0004c0011t0004g0021 a0004c0011t0004g0278 others(2): Show |
6 | HG02258.hp1 HG02280.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-1211C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451773 | |||||||
chr19:1451799 | C | T | 1 | a0003c0007t0006g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18-1185C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451799 | |||||||
chr19:1451820 | G | A | 1 | a0001c0003t0034g0025 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-18-1164G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451820 | |||||||
chr19:1451841 | C | G | 5 | a0001c0001t0001g0280 a0004c0011t0004g0021 a0004c0011t0004g0278 others(2): Show |
6 | HG02258.hp1 HG02280.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-1143C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451841 | |||||||
chr19:1451988 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-18-996G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1451988 | |||||||
chr19:1452012 | G | C | 2 | a0002c0002t0002g0271 a0002c0002t0002g0272 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-18-972G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452012 | |||||||
chr19:1452053 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-18-931C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452053 | |||||||
chr19:1452131 | C | T | 2 | a0002c0002t0002g0271 a0002c0002t0002g0272 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-18-853C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452131 | |||||||
chr19:1452161 | G | A | 3 | a0002c0002t0002g0271 a0002c0002t0002g0272 a0002c0002t0002g0273 |
3 | HG02145.hp2 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-823G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452161 | |||||||
chr19:1452163 | C | T | 1 | a0002c0002t0002g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-18-821C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452163 | |||||||
chr19:1452232 | G | A | 3 | a0001c0001t0001g0230 a0001c0001t0032g0228 a0001c0056t0001g0229 |
3 | HG01891.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-752G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452232 | |||||||
chr19:1452234 | G | A | 9 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(6): Show |
10 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-750G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452234 | |||||||
chr19:1452240 | A | G | 27 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0230 others(24): Show |
27 | HG01192.hp1 HG01516.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-744A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452240 | |||||||
chr19:1452249 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0035 others(4): Show |
9 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-735G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452249 | |||||||
chr19:1452297 | G | T | 3 | a0004c0009t0004g0264 a0005c0004t0003g0020 a0020c0029t0003g0020 |
3 | HG02723.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-18-687G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452297 | |||||||
chr19:1452443 | T | G | 12 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(9): Show |
14 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18-541T>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452443 | |||||||
chr19:1452466 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18-518G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452466 | |||||||
chr19:1452473 | G | A | 1 | a0001c0003t0001g0039 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-18-511G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452473 | |||||||
chr19:1452484 | C | T | 16 | a0001c0001t0001g0230 a0001c0001t0001g0254 a0001c0001t0001g0255 others(13): Show |
16 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18-500C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452484 | |||||||
chr19:1452492 | G | C | 35 | a0001c0001t0001g0172 a0001c0001t0001g0230 a0001c0001t0001g0232 others(32): Show |
35 | HG00733.hp1 HG01192.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-18-492G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452492 | |||||||
chr19:1452523 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18-461C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452523 | |||||||
chr19:1452611 | G | T | 1 | a0003c0006t0047g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18-373G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452611 | |||||||
chr19:1452644 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18-340G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452644 | |||||||
chr19:1452666 | G | A | 1 | a0001c0003t0001g0042 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-18-318G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452666 | |||||||
chr19:1452702 | C | T | 1 | a0002c0002t0002g0157 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-18-282C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452702 | |||||||
chr19:1452816 | C | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(214): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-18-168C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | chr19 | 1452816 | |||||||
chr19:1452863 | A | AC | 28 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0230 others(25): Show |
30 | HG00597.hp2 HG01175.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-18-113dupC | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 1452863 | ||||||
chr19:1453161 | G | A | 30 | a0001c0001t0001g0172 a0001c0001t0001g0230 a0001c0001t0001g0232 others(27): Show |
30 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.141+19G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 2/14 | chr19 | 1453161 | |||||||
chr19:1453164 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141+22G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 2/14 | chr19 | 1453164 | |||||||
chr19:1453224 | C | T | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-23C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 2/14 | chr19 | 1453224 | |||||||
chr19:1453400 | G | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0221 |
2 | HG02027.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.233-31G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 3/14 | chr19 | 1453400 | |||||||
chr19:1453706 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.413+95T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453706 | |||||||
chr19:1453722 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0009g0242 |
2 | HG00733.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.413+111G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453722 | |||||||
chr19:1453856 | C | T | 2 | a0001c0046t0023g0241 a0004c0047t0042g0240 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.413+245C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453856 | |||||||
chr19:1453899 | A | T | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+288A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453899 | |||||||
chr19:1453912 | T | A | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+301T>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453912 | |||||||
chr19:1453913 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.413+302C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453913 | |||||||
chr19:1453921 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+310A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453921 | |||||||
chr19:1453979 | C | A | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+368C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1453979 | |||||||
chr19:1454010 | G | T | 14 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0237 others(11): Show |
14 | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+399G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454010 | |||||||
chr19:1454043 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(221): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.413+432T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454043 | |||||||
chr19:1454061 | G | C | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+450G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454061 | |||||||
chr19:1454073 | G | A | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+462G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454073 | |||||||
chr19:1454364 | CT | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(175): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.413+767delT | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454364 | ||||||
chr19:1454364 | CTT | C | 11 | a0001c0001t0001g0054 a0001c0001t0001g0172 a0001c0062t0030g0151 others(8): Show |
11 | HG01975.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+766_413+767del others(2): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454364 | ||||||
chr19:1454364 | CTTT | C | 29 | a0001c0001t0001g0230 a0001c0001t0001g0232 a0001c0001t0001g0235 others(26): Show |
29 | HG00733.hp1 HG01192.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.413+765_413+767del others(3): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454364 | ||||||
chr19:1454471 | T | C | 17 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(14): Show |
19 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.414-678T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454471 | |||||||
chr19:1454563 | C | CT | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(163): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.414-568dupT | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454563 | ||||||
chr19:1454563 | C | CTT | 33 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0172 others(30): Show |
34 | HG01109.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.414-569_414-568dup others(2): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454563 | ||||||
chr19:1454563 | C | CTTT | 20 | a0001c0001t0001g0230 a0001c0001t0001g0255 a0001c0001t0001g0259 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-570_414-568dup others(3): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454563 | ||||||
chr19:1454563 | C | CTTTTCTT others(10): Show |
1 | a0001c0001t0009g0242 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.414-582_414-581ins others(17): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454563 | ||||||
chr19:1454563 | CT | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0184 a0001c0028t0005g0185 others(4): Show |
10 | HG01516.hp2 HG02723.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-568delT | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454563 | ||||||
chr19:1454586 | C | T | 9 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-563C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454586 | |||||||
chr19:1454602 | C | T | 9 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-547C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454602 | |||||||
chr19:1454607 | A | G | 9 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-542A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454607 | |||||||
chr19:1454608 | A | G | 48 | a0001c0001t0001g0172 a0001c0001t0001g0230 a0001c0001t0001g0232 others(45): Show |
49 | HG00733.hp1 HG01192.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.414-541A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454608 | |||||||
chr19:1454656 | C | T | 3 | a0004c0011t0004g0021 a0004c0011t0004g0278 a0004c0011t0004g0279 |
4 | HG03130.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-493C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454656 | |||||||
chr19:1454666 | C | G | 3 | a0004c0011t0004g0021 a0004c0011t0004g0278 a0004c0011t0004g0279 |
4 | HG03130.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-483C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454666 | |||||||
chr19:1454691 | G | C | 27 | a0001c0001t0001g0172 a0001c0001t0001g0230 a0001c0001t0001g0232 others(24): Show |
27 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.414-458G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454691 | |||||||
chr19:1454740 | C | T | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-409C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454740 | |||||||
chr19:1454792 | C | T | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-357C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454792 | |||||||
chr19:1454809 | C | T | 1 | a0001c0001t0007g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414-340C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454809 | |||||||
chr19:1454846 | C | A | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-303C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454846 | |||||||
chr19:1454970 | G | A | 51 | a0001c0001t0001g0172 a0001c0001t0001g0230 a0001c0001t0001g0232 others(48): Show |
52 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.414-179G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1454970 | |||||||
chr19:1454986 | A | AC | 17 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0049 others(14): Show |
17 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.414-152dupC | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454986 | ||||||
chr19:1454986 | AC | A | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.414-152delC | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454986 | ||||||
chr19:1454986 | ACC | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0035 others(44): Show |
51 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.414-153_414-152del others(2): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 1454986 | ||||||
chr19:1455031 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.414-118C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 4/14 | chr19 | 1455031 | |||||||
chr19:1455319 | G | T | 12 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0237 others(9): Show |
12 | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+62G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 5/14 | chr19 | 1455319 | |||||||
chr19:1455518 | G | T | 1 | a0001c0001t0033g0210 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.639+18G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | chr19 | 1455518 | |||||||
chr19:1455629 | C | T | 8 | a0001c0001t0001g0230 a0001c0001t0001g0255 a0001c0001t0032g0228 others(5): Show |
8 | HG01884.hp2 HG01891.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+129C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | chr19 | 1455629 | |||||||
chr19:1455639 | T | C | 5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+139T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | chr19 | 1455639 | |||||||
chr19:1455668 | G | T | 2 | a0008c0018t0001g0169 a0008c0018t0001g0170 |
2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.639+168G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | chr19 | 1455668 | |||||||
chr19:1455784 | G | A | 2 | a0001c0001t0001g0172 a0002c0002t0048g0173 |
2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.639+284G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | chr19 | 1455784 | |||||||
chr19:1455904 | G | T | 8 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(5): Show |
9 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.640-172G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | chr19 | 1455904 | |||||||
chr19:1455934 | C | CAGAGTCA others(26): Show |
201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(198): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.640-138_640-137ins others(33): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 1455934 | ||||||
chr19:1456206 | C | T | 1 | a0004c0010t0004g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.717+53C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 7/14 | chr19 | 1456206 | |||||||
chr19:1456213 | C | T | 6 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0044g0281 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+60C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 7/14 | chr19 | 1456213 | |||||||
chr19:1456290 | G | C | 1 | a0001c0001t0038g0043 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.718-16G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 7/14 | chr19 | 1456290 | |||||||
chr19:1456474 | C | T | 1 | a0002c0002t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+70C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456474 | |||||||
chr19:1456545 | A | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(214): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.816+141A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456545 | |||||||
chr19:1456591 | G | A | 3 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0019c0035t0002g0068 |
3 | HG02976.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.816+187G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456591 | |||||||
chr19:1456596 | G | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.816+192G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456596 | |||||||
chr19:1456613 | G | A | 8 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0002g0271 others(5): Show |
8 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+209G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456613 | |||||||
chr19:1456648 | C | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(212): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.817-205C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456648 | |||||||
chr19:1456654 | G | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(212): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.817-199G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456654 | |||||||
chr19:1456659 | C | A | 28 | a0001c0001t0001g0230 a0001c0001t0001g0232 a0001c0001t0001g0235 others(25): Show |
28 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.817-194C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456659 | |||||||
chr19:1456667 | A | C | 8 | a0001c0001t0037g0269 a0002c0002t0002g0181 a0002c0002t0002g0271 others(5): Show |
8 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-186A>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456667 | |||||||
chr19:1456718 | C | G | 1 | a0001c0001t0018g0141 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.817-135C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456718 | |||||||
chr19:1456731 | G | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(150): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.817-122G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456731 | |||||||
chr19:1456807 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.817-46C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456807 | |||||||
chr19:1456820 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0009g0242 |
2 | HG00733.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.817-33A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 8/14 | chr19 | 1456820 | |||||||
chr19:1457287 | C | T | 1 | a0005c0004t0003g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1207+44C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457287 | |||||||
chr19:1457371 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(178): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1207+128C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457371 | |||||||
chr19:1457404 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1207+161G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457404 | |||||||
chr19:1457479 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(179): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1207+236T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457479 | |||||||
chr19:1457496 | T | C | 43 | a0001c0001t0001g0080 a0001c0001t0001g0232 a0001c0001t0001g0235 others(40): Show |
44 | HG01192.hp1 HG01192.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1207+253T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457496 | |||||||
chr19:1457510 | T | C | 1 | a0001c0001t0009g0242 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1207+267T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457510 | |||||||
chr19:1457518 | T | C | 8 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(5): Show |
9 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207+275T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457518 | |||||||
chr19:1457531 | G | A | 10 | a0001c0001t0001g0033 a0001c0001t0001g0167 a0001c0001t0001g0246 others(7): Show |
10 | HG00738.hp1 HG01358.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+288G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457531 | |||||||
chr19:1457552 | G | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1207+309G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457552 | |||||||
chr19:1457691 | C | T | 1 | a0001c0019t0001g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1208-274C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457691 | |||||||
chr19:1457876 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1208-89G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457876 | |||||||
chr19:1457895 | C | CCGGGGGG others(4): Show |
1 | a0002c0002t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1208-70_1208-69ins others(11): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(6): Show |
4 | a0001c0001t0001g0280 a0002c0002t0002g0238 a0003c0007t0006g0256 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(13): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(7): Show |
8 | a0001c0001t0001g0232 a0001c0032t0001g0158 a0003c0007t0006g0257 others(5): Show |
8 | HG01978.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(14): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(8): Show |
5 | a0001c0001t0001g0235 a0004c0009t0019g0234 a0004c0009t0040g0233 others(2): Show |
5 | HG01192.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(15): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(9): Show |
3 | a0001c0001t0001g0237 a0001c0046t0023g0241 a0005c0004t0003g0236 |
3 | HG01884.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(16): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(10): Show |
2 | a0001c0001t0001g0080 a0001c0001t0026g0262 |
2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(17): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(11): Show |
2 | a0001c0001t0032g0228 a0003c0007t0006g0265 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(18): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(13): Show |
1 | a0014c0058t0020g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1208-70_1208-69ins others(20): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(14): Show |
4 | a0002c0002t0002g0066 a0004c0009t0004g0264 a0004c0010t0004g0061 others(1): Show |
4 | HG02976.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(21): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(15): Show |
5 | a0002c0002t0002g0067 a0002c0002t0002g0266 a0002c0002t0049g0182 others(2): Show |
6 | HG01891.hp1 HG03209.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(22): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(16): Show |
2 | a0002c0002t0002g0267 a0019c0035t0002g0068 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(23): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(17): Show |
1 | a0003c0061t0012g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1208-70_1208-69ins others(24): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(18): Show |
2 | a0001c0062t0030g0151 a0016c0064t0004g0057 |
2 | HG02486.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(25): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(19): Show |
1 | a0004c0010t0004g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1208-70_1208-69ins others(26): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(20): Show |
2 | a0002c0002t0002g0268 a0004c0010t0004g0059 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1208-70_1208-69ins others(27): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CCGGGGGG others(21): Show |
1 | a0005c0060t0021g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1208-70_1208-69ins others(28): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457895 | |||||||
chr19:1457895 | C | CGGGGGGC others(3): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0142 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1208-67_1208-66ins others(10): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(2): Show |
48 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0044 others(45): Show |
58 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1208-67_1208-66ins others(9): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(3): Show |
65 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(62): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1208-67_1208-66ins others(10): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(4): Show |
32 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0040 others(29): Show |
32 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1208-67_1208-66ins others(11): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(5): Show |
9 | a0001c0001t0001g0065 a0001c0001t0001g0135 a0001c0001t0001g0136 others(6): Show |
9 | HG00558.hp1 HG00733.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1208-67_1208-66ins others(12): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(6): Show |
3 | a0001c0001t0001g0254 a0001c0056t0001g0229 a0002c0002t0002g0181 |
3 | HG02683.hp2 HG03471.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1208-67_1208-66ins others(13): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(9): Show |
1 | a0001c0001t0001g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1208-67_1208-66ins others(16): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457895 | C | CGGGGGGG others(11): Show |
1 | a0001c0001t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1208-67_1208-66ins others(18): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 1457895 | ||||||
chr19:1457898 | G | GGGGGGGG others(3): Show |
1 | a0006c0012t0001g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1208-67_1208-66ins others(10): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 9/14 | chr19 | 1457898 | |||||||
chr19:1458125 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1303+65C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458125 | |||||||
chr19:1458126 | G | A | 38 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0237 others(35): Show |
39 | HG00733.hp2 HG01192.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.1303+66G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458126 | |||||||
chr19:1458162 | C | T | 2 | a0002c0002t0002g0181 a0029c0026t0002g0180 |
2 | NA18982.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1303+102C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458162 | |||||||
chr19:1458178 | G | A | 17 | a0001c0001t0001g0033 a0001c0001t0001g0167 a0001c0001t0001g0246 others(14): Show |
20 | HG00738.hp1 HG01358.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1303+118G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458178 | |||||||
chr19:1458212 | C | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0230 a0001c0001t0001g0254 others(6): Show |
9 | HG00733.hp1 HG01891.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1303+152C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458212 | |||||||
chr19:1458227 | C | T | 1 | a0002c0002t0002g0181 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1303+167C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458227 | |||||||
chr19:1458289 | C | T | 2 | a0008c0018t0001g0169 a0008c0018t0001g0170 |
2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1303+229C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458289 | |||||||
chr19:1458290 | G | A | 2 | a0001c0001t0001g0172 a0002c0002t0048g0173 |
2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1303+230G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458290 | |||||||
chr19:1458304 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1303+244G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458304 | |||||||
chr19:1458337 | G | A | 1 | a0007c0021t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1303+277G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458337 | |||||||
chr19:1458346 | G | C | 2 | a0002c0002t0002g0238 a0003c0015t0012g0165 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1303+286G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458346 | |||||||
chr19:1458426 | C | T | 1 | a0003c0007t0006g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1303+366C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458426 | |||||||
chr19:1458430 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1303+370G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458430 | |||||||
chr19:1458568 | T | C | 3 | a0001c0001t0001g0015 a0001c0016t0001g0015 a0001c0016t0001g0117 |
3 | NA18963.hp2 NA18966.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1303+508T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458568 | |||||||
chr19:1458633 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1303+573G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458633 | |||||||
chr19:1458685 | C | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0248 a0001c0001t0001g0252 |
3 | HG02602.hp1 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1303+625C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458685 | |||||||
chr19:1458718 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1303+658T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458718 | |||||||
chr19:1458827 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1303+767G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458827 | |||||||
chr19:1458833 | G | A | 2 | a0002c0002t0002g0271 a0002c0002t0002g0272 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1303+773G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458833 | |||||||
chr19:1458840 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1303+780C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458840 | |||||||
chr19:1458918 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(207): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1303+858G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458918 | |||||||
chr19:1458926 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1303+866C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458926 | |||||||
chr19:1458952 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1303+892G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1458952 | |||||||
chr19:1459009 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1303+949G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459009 | |||||||
chr19:1459092 | C | G | 1 | a0003c0007t0006g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1303+1032C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459092 | |||||||
chr19:1459144 | C | T | 1 | a0005c0004t0003g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1304-1037C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459144 | |||||||
chr19:1459236 | G | C | 1 | a0001c0001t0007g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1304-945G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459236 | |||||||
chr19:1459267 | C | T | 1 | a0003c0007t0006g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1304-914C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459267 | |||||||
chr19:1459268 | C | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(222): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1304-913C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459268 | |||||||
chr19:1459307 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1304-874C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459307 | |||||||
chr19:1459425 | A | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0254 a0001c0001t0009g0037 others(6): Show |
9 | HG01167.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1304-756A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459425 | |||||||
chr19:1459470 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1304-711C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459470 | |||||||
chr19:1459492 | C | T | 1 | a0003c0007t0006g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1304-689C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459492 | |||||||
chr19:1459515 | A | G | 4 | a0005c0004t0003g0005 a0005c0004t0003g0020 a0005c0004t0003g0243 others(1): Show |
7 | HG02723.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1304-666A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459515 | |||||||
chr19:1459742 | G | A | 1 | a0004c0009t0040g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1304-439G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459742 | |||||||
chr19:1459893 | G | A | 1 | a0001c0030t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1304-288G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459893 | |||||||
chr19:1459907 | A | T | 2 | a0001c0001t0001g0143 a0017c0051t0001g0208 |
2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1304-274A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1459907 | |||||||
chr19:1459960 | C | CG | 6 | a0001c0001t0001g0038 a0001c0001t0001g0118 a0001c0001t0010g0086 others(3): Show |
6 | HG01192.hp1 HG02148.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1304-216dupG | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 1459960 | ||||||
chr19:1460037 | G | A | 55 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
57 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1304-144G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 10/14 | chr19 | 1460037 | |||||||
chr19:1460471 | T | C | 8 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0167 others(5): Show |
8 | HG01192.hp1 HG01978.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1443+151T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460471 | |||||||
chr19:1460474 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(58): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1443+154G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460474 | |||||||
chr19:1460589 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1444-191C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460589 | |||||||
chr19:1460590 | G | A | 1 | a0033c0025t0039g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1444-190G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460590 | |||||||
chr19:1460607 | CCT | C | 6 | a0001c0062t0030g0151 a0004c0010t0004g0058 a0004c0010t0004g0059 others(3): Show |
6 | HG02486.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1444-172_1444-171d others(4): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460607 | |||||||
chr19:1460678 | G | A | 10 | a0001c0062t0030g0151 a0003c0015t0012g0161 a0003c0015t0012g0165 others(7): Show |
10 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444-102G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460678 | |||||||
chr19:1460752 | G | A | 1 | a0003c0061t0012g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1444-28G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 11/14 | chr19 | 1460752 | |||||||
chr19:1460915 | T | C | 9 | a0005c0004t0003g0005 a0005c0004t0003g0020 a0005c0004t0003g0168 others(6): Show |
12 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1521+58T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/14 | chr19 | 1460915 | |||||||
chr19:1460923 | G | A | 1 | a0001c0001t0015g0009 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1521+66G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/14 | chr19 | 1460923 | |||||||
chr19:1460946 | T | C | 4 | a0002c0002t0048g0173 a0003c0006t0047g0263 a0003c0017t0045g0253 others(1): Show |
4 | HG02630.hp2 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521+89T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/14 | chr19 | 1460946 | |||||||
chr19:1460999 | A | G | 38 | a0001c0001t0001g0069 a0001c0001t0001g0232 a0001c0001t0001g0235 others(35): Show |
40 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.1522-38A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 12/14 | chr19 | 1460999 | |||||||
chr19:1461230 | C | T | 6 | a0003c0007t0006g0028 a0003c0007t0006g0032 a0003c0007t0006g0256 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638+77C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461230 | |||||||
chr19:1461272 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0145 others(1): Show |
4 | NA18939.hp2 NA18941.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638+119G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461272 | |||||||
chr19:1461295 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1638+142G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461295 | |||||||
chr19:1461412 | T | TA | 10 | a0001c0062t0030g0151 a0003c0015t0012g0161 a0003c0015t0012g0165 others(7): Show |
10 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1638+267dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 1461412 | ||||||
chr19:1461459 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1638+306C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461459 | |||||||
chr19:1461464 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1638+311G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461464 | |||||||
chr19:1461501 | G | A | 1 | a0021c0044t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1638+348G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461501 | |||||||
chr19:1461529 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1638+376G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461529 | |||||||
chr19:1461589 | T | A | 84 | a0001c0001t0001g0069 a0001c0001t0001g0111 a0001c0001t0001g0232 others(81): Show |
89 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(86): Show |
intron_variant | MODIFIER | c.1639-374T>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461589 | |||||||
chr19:1461590 | T | C | 74 | a0001c0001t0001g0069 a0001c0001t0001g0111 a0001c0001t0001g0232 others(71): Show |
79 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(76): Show |
intron_variant | MODIFIER | c.1639-373T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461590 | |||||||
chr19:1461618 | C | T | 12 | a0002c0002t0002g0266 a0002c0002t0002g0267 a0002c0002t0002g0268 others(9): Show |
15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1639-345C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461618 | |||||||
chr19:1461628 | G | A | 6 | a0003c0007t0006g0028 a0003c0007t0006g0032 a0003c0007t0006g0256 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639-335G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461628 | |||||||
chr19:1461635 | A | G | 6 | a0003c0007t0006g0028 a0003c0007t0006g0032 a0003c0007t0006g0256 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639-328A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461635 | |||||||
chr19:1461663 | T | C | 6 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-300T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461663 | |||||||
chr19:1461668 | C | A | 7 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0237 others(4): Show |
7 | HG01192.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-295C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461668 | |||||||
chr19:1461669 | G | A | 16 | a0001c0062t0030g0151 a0003c0007t0006g0028 a0003c0007t0006g0032 others(13): Show |
16 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1639-294G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461669 | |||||||
chr19:1461699 | A | G | 1 | a0009c0043t0001g0219 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1639-264A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461699 | |||||||
chr19:1461712 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1639-251C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461712 | |||||||
chr19:1461721 | G | A | 7 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0237 others(4): Show |
7 | HG01192.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-242G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461721 | |||||||
chr19:1461783 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0167 others(1): Show |
4 | HG02602.hp1 HG02602.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-180C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461783 | |||||||
chr19:1461851 | C | CA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0093 a0001c0001t0001g0112 others(10): Show |
13 | HG01978.hp1 HG02027.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1639-100dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 1461851 | ||||||
chr19:1461851 | CA | C | 11 | a0001c0001t0037g0269 a0001c0062t0030g0151 a0003c0015t0012g0161 others(8): Show |
11 | HG02257.hp2 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639-100delA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 1461851 | ||||||
chr19:1461863 | A | C | 61 | a0001c0001t0001g0111 a0001c0001t0001g0232 a0001c0001t0001g0235 others(58): Show |
66 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(63): Show |
intron_variant | MODIFIER | c.1639-100A>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461863 | |||||||
chr19:1461864 | C | A | 62 | a0001c0001t0001g0111 a0001c0001t0001g0232 a0001c0001t0001g0235 others(59): Show |
67 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(64): Show |
intron_variant | MODIFIER | c.1639-99C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461864 | |||||||
chr19:1461864 | C | CA | 4 | a0002c0002t0048g0173 a0003c0006t0013g0202 a0003c0006t0047g0263 others(1): Show |
4 | HG02630.hp2 HG02698.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-93dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 1461864 | ||||||
chr19:1461876 | A | G | 13 | a0001c0001t0001g0111 a0001c0001t0001g0246 a0001c0001t0001g0252 others(10): Show |
14 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1639-87A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461876 | |||||||
chr19:1461918 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1639-45G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 13/14 | chr19 | 1461918 | |||||||
chr19:1462181 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01993.hp2 | splice_region_variant&intron_variant | LOW | c.1853+4G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462181 | |||||||
chr19:1462193 | C | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0126 others(3): Show |
6 | HG02074.hp1 HG02132.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1853+16C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462193 | |||||||
chr19:1462257 | G | A | 1 | a0010c0037t0001g0081 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1853+80G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462257 | |||||||
chr19:1462299 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1853+122C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462299 | |||||||
chr19:1462331 | T | G | 28 | a0001c0001t0001g0246 a0001c0001t0001g0252 a0001c0046t0023g0241 others(25): Show |
32 | HG01109.hp2 HG01243.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1853+154T>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462331 | |||||||
chr19:1462334 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1853+157A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462334 | |||||||
chr19:1462421 | C | T | 1 | a0001c0001t0037g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1853+244C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462421 | |||||||
chr19:1462429 | G | A | 18 | a0001c0001t0007g0144 a0002c0002t0002g0027 a0002c0002t0002g0066 others(15): Show |
18 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1853+252G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462429 | |||||||
chr19:1462590 | G | A | 1 | a0001c0020t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1853+413G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462590 | |||||||
chr19:1462655 | C | CA | 30 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0089 others(27): Show |
30 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1853+504dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462655 | C | CAA | 6 | a0005c0004t0003g0005 a0005c0004t0003g0020 a0005c0004t0003g0168 others(3): Show |
9 | HG02257.hp1 HG02451.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1853+503_1853+504d others(4): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462655 | C | CAAAA | 6 | a0001c0001t0001g0260 a0001c0046t0023g0241 a0002c0002t0002g0267 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1853+501_1853+504d others(6): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462655 | C | CAAAAA | 15 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0002c0002t0002g0027 others(12): Show |
16 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1853+500_1853+504d others(7): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462655 | C | CAAAAAA | 7 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(4): Show |
8 | HG01192.hp1 HG01891.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1853+499_1853+504d others(8): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462655 | CA | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0062 others(29): Show |
34 | HG00323.hp1 HG00558.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1853+504delA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462655 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1853+494_1853+504d others(13): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462655 | ||||||
chr19:1462727 | T | C | 2 | a0002c0002t0002g0181 a0029c0026t0002g0180 |
2 | NA18982.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1853+550T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462727 | |||||||
chr19:1462741 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1853+564C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462741 | |||||||
chr19:1462746 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1853+569G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462746 | |||||||
chr19:1462779 | C | G | 9 | a0001c0001t0001g0232 a0001c0001t0001g0280 a0004c0009t0004g0264 others(6): Show |
10 | HG01192.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1853+602C>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462779 | |||||||
chr19:1462794 | C | T | 53 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(50): Show |
58 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.1853+617C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462794 | |||||||
chr19:1462837 | G | A | 1 | a0001c0005t0043g0052 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1853+660G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462837 | |||||||
chr19:1462903 | G | A | 9 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(6): Show |
11 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1853+726G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462903 | |||||||
chr19:1462914 | T | A | 34 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(31): Show |
36 | HG01192.hp1 HG01891.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.1853+737T>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462914 | |||||||
chr19:1462943 | A | T | 1 | a0030c0052t0031g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1853+766A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462943 | |||||||
chr19:1462970 | T | TA | 8 | a0001c0001t0001g0072 a0001c0001t0001g0176 a0001c0001t0001g0226 others(5): Show |
8 | HG01175.hp2 HG02027.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1853+808dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462970 | ||||||
chr19:1462970 | TA | T | 48 | a0001c0001t0001g0093 a0001c0001t0001g0184 a0001c0001t0001g0246 others(45): Show |
51 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1853+808delA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1462970 | ||||||
chr19:1462992 | C | A | 1 | a0001c0008t0001g0023 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1853+815C>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1462992 | |||||||
chr19:1463049 | G | A | 1 | a0005c0004t0003g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1853+872G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463049 | |||||||
chr19:1463093 | T | C | 1 | a0001c0003t0001g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1853+916T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463093 | |||||||
chr19:1463266 | A | C | 65 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(62): Show |
70 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.1853+1089A>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463266 | |||||||
chr19:1463280 | T | C | 1 | a0033c0025t0039g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1853+1103T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463280 | |||||||
chr19:1463315 | G | C | 7 | a0001c0046t0023g0241 a0003c0007t0006g0028 a0003c0007t0006g0032 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1853+1138G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463315 | |||||||
chr19:1463343 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1853+1166G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463343 | |||||||
chr19:1463398 | A | G | 1 | a0033c0025t0039g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1853+1221A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463398 | |||||||
chr19:1463416 | C | CA | 25 | a0001c0001t0001g0041 a0001c0001t0001g0122 a0001c0001t0001g0128 others(22): Show |
25 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1853+1256dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463416 | ||||||
chr19:1463416 | C | CAA | 43 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(40): Show |
45 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.1853+1255_1853+125 others(6): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463416 | ||||||
chr19:1463416 | C | CAAA | 15 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(12): Show |
18 | HG01192.hp1 HG01978.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1853+1254_1853+125 others(7): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463416 | ||||||
chr19:1463416 | CA | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0280 a0001c0001t0005g0225 others(3): Show |
6 | HG02280.hp1 NA18941.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1853+1256delA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463416 | ||||||
chr19:1463437 | A | G | 64 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(61): Show |
69 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(66): Show |
intron_variant | MODIFIER | c.1853+1260A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463437 | |||||||
chr19:1463539 | G | T | 77 | a0001c0001t0001g0246 a0001c0001t0001g0252 a0001c0001t0001g0259 others(74): Show |
82 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(79): Show |
intron_variant | MODIFIER | c.1853+1362G>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463539 | |||||||
chr19:1463581 | C | CA | 39 | a0001c0001t0001g0089 a0001c0001t0001g0097 a0001c0001t0001g0127 others(36): Show |
39 | HG00738.hp2 HG01255.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1853+1420dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463581 | ||||||
chr19:1463581 | C | CAA | 7 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0027g0031 others(4): Show |
9 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1853+1419_1853+142 others(6): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463581 | ||||||
chr19:1463581 | CA | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0196 a0001c0001t0001g0201 others(5): Show |
8 | HG00323.hp2 HG00609.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1853+1420delA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1463581 | ||||||
chr19:1463900 | C | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0252 a0003c0006t0011g0133 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1854-1255C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463900 | |||||||
chr19:1463983 | C | T | 4 | a0004c0009t0019g0234 a0004c0009t0040g0233 a0004c0009t0041g0231 others(1): Show |
4 | HG01192.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1854-1172C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1463983 | |||||||
chr19:1464004 | G | A | 1 | a0033c0025t0039g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1854-1151G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464004 | |||||||
chr19:1464011 | A | C | 5 | a0001c0046t0023g0241 a0004c0009t0019g0234 a0004c0009t0040g0233 others(2): Show |
5 | HG01192.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1854-1144A>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464011 | |||||||
chr19:1464074 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0246 |
2 | HG02074.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1854-1081C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464074 | |||||||
chr19:1464095 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1854-1060G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464095 | |||||||
chr19:1464101 | G | A | 3 | a0003c0006t0047g0263 a0003c0017t0045g0253 a0003c0017t0046g0171 |
3 | HG02630.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1854-1054G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464101 | |||||||
chr19:1464184 | C | T | 1 | a0001c0062t0030g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1854-971C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464184 | |||||||
chr19:1464311 | G | GA | 7 | a0001c0046t0023g0241 a0003c0007t0006g0028 a0003c0007t0006g0032 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854-833dupA | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1464311 | ||||||
chr19:1464314 | A | G | 36 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(33): Show |
38 | HG01192.hp1 HG01891.hp1 HG01978.hp2 others(35): Show |
intron_variant | MODIFIER | c.1854-841A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464314 | |||||||
chr19:1464340 | T | C | 7 | a0001c0046t0023g0241 a0003c0007t0006g0028 a0003c0007t0006g0032 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854-815T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464340 | |||||||
chr19:1464404 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1854-751T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464404 | |||||||
chr19:1464538 | A | G | 11 | a0001c0046t0023g0241 a0003c0007t0006g0028 a0003c0007t0006g0032 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1854-617A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464538 | |||||||
chr19:1464542 | C | T | 1 | a0001c0001t0017g0108 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1854-613C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464542 | |||||||
chr19:1464543 | G | A | 1 | a0001c0001t0037g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1854-612G>A | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464543 | |||||||
chr19:1464561 | A | G | 1 | a0001c0059t0001g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1854-594A>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464561 | |||||||
chr19:1464567 | A | T | 1 | a0002c0002t0044g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1854-588A>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464567 | |||||||
chr19:1464632 | C | CT | 36 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0119 others(33): Show |
36 | HG00735.hp1 HG01109.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.1854-504dupT | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1464632 | ||||||
chr19:1464632 | C | CTT | 38 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0027g0031 others(35): Show |
40 | HG01192.hp2 HG01243.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1854-505_1854-504d others(4): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1464632 | ||||||
chr19:1464632 | CT | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0073 a0001c0001t0001g0088 others(8): Show |
11 | HG00323.hp1 HG01169.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1854-504delT | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1464632 | ||||||
chr19:1464654 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1854-501G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464654 | |||||||
chr19:1464689 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1854-466G>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464689 | |||||||
chr19:1464693 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1854-462C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464693 | |||||||
chr19:1464725 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1854-430C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464725 | |||||||
chr19:1464771 | T | C | 56 | a0001c0001t0001g0246 a0001c0001t0001g0252 a0001c0001t0007g0010 others(53): Show |
61 | HG01109.hp2 HG01243.hp1 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.1854-384T>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464771 | |||||||
chr19:1464783 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1854-372C>T | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464783 | |||||||
chr19:1464912 | T | G | 1 | a0024c0034t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1854-243T>G | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464912 | |||||||
chr19:1464936 | C | CT | 49 | a0001c0001t0007g0010 a0001c0001t0007g0029 a0001c0001t0007g0030 others(46): Show |
54 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.1854-205dupT | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1464936 | ||||||
chr19:1464936 | C | CTT | 6 | a0002c0002t0002g0273 a0003c0006t0011g0133 a0003c0006t0011g0203 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1854-206_1854-205d others(4): Show |
APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 1464936 | ||||||
chr19:1464952 | A | C | 13 | a0004c0009t0004g0264 a0004c0009t0019g0234 a0004c0009t0040g0233 others(10): Show |
14 | HG01192.hp2 HG02486.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1854-203A>C | APC2 | ENSG00000115266.12 | transcript | ENST00000590469.6 | protein_coding | 14/14 | chr19 | 1464952 |