Item | Value |
---|---|
geneid | 55037 |
ensemblid | ENSG00000132300.19 |
hgncid | 24717 |
symbol | PTCD3 |
name | pentatricopeptide repeat domain 3 |
refseq_nuc | NM_017952.6 |
refseq_prot | NP_060422.4 |
ensembl_nuc | ENST00000254630.12 |
ensembl_prot | ENSP00000254630.7 |
mane_status | MANE Select |
chr | chr2 |
start | 86106235 |
end | 86142157 |
strand | + |
ver | v1.2 |
region | chr2:86106235-86142157 |
region5000 | chr2:86101235-86147157 |
regionname0 | PTCD3_chr2_86106235_86142157 |
regionname5000 | PTCD3_chr2_86101235_86147157 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 689 | 328 | 71 | 70 | 138 | 10 | 37 | 108 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0002 | 0/0 | 689 | 50 | 0 | 0 | 46 | 0 | 4 | 37 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0003 | 0/0 | 689 | 15 | 15 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | MVVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0004 | 0/0 | 689 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0005 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0006 | 0/0 | 689 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0007 | 0/0 | 689 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
a0008 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | MAVVS others(684): Show |
chr2 | 86101235 | 86147157 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2067 | 308 | 58 | 66 | 138 | 9 | 35 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0001c0003 | 0/0 | 2067 | 18 | 11 | 4 | 0 | 1 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0001c0006 | 0/0 | 2067 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0002c0002 | 0/0 | 2067 | 47 | 0 | 0 | 43 | 0 | 4 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0002c0005 | 0/0 | 2067 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0003c0004 | 0/0 | 2067 | 15 | 15 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGT others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0004c0009 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0005c0007 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0006c0011 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0007c0010 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 | ||
a0008c0008 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | ATGGC others(2062): Show |
chr2 | 86101235 | 86147157 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6681 | 92 | 0 | 24 | 50 | 2 | 16 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0002 | 0/0 | 6683 | 56 | 3 | 20 | 23 | 4 | 6 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0003 | 0/0 | 6680 | 35 | 0 | 4 | 29 | 2 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0005 | 0/0 | 6681 | 19 | 8 | 1 | 3 | 0 | 7 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0006 | 0/0 | 6679 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0009 | 0/0 | 6682 | 7 | 0 | 0 | 7 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6677): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0010 | 0/0 | 6684 | 5 | 1 | 2 | 0 | 0 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0011 | 0/0 | 6684 | 6 | 0 | 0 | 5 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0012 | 0/0 | 6677 | 5 | 5 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6672): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0013 | 0/0 | 6682 | 5 | 0 | 2 | 3 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6677): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0014 | 0/0 | 6682 | 4 | 1 | 3 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6677): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0015 | 0/0 | 6681 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0016 | 0/0 | 6676 | 4 | 3 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6671): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0017 | 0/0 | 6676 | 4 | 3 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6671): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0018 | 0/0 | 6676 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6671): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0021 | 0/0 | 6683 | 4 | 0 | 3 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0023 | 0/0 | 6660 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6655): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0024 | 0/0 | 6678 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6673): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0025 | 0/0 | 6677 | 3 | 2 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6672): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0028 | 0/0 | 6677 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6672): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0029 | 0/0 | 6677 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6672): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0030 | 0/0 | 6681 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0031 | 0/0 | 6683 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0032 | 0/0 | 6681 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0033 | 0/0 | 6682 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6677): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0035 | 0/0 | 6681 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0036 | 0/0 | 6677 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6672): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0037 | 0/0 | 6684 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0038 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0039 | 0/0 | 6681 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0040 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0041 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0042 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0043 | 0/0 | 6684 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0044 | 1/0 | 6681 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0045 | 0/0 | 6676 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6671): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0047 | 0/1 | 6685 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6680): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0048 | 0/0 | 6685 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6680): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0049 | 0/0 | 6683 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0050 | 0/0 | 6683 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0051 | 0/0 | 6684 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0052 | 0/0 | 6678 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6673): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0053 | 0/0 | 6677 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6672): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0054 | 0/0 | 6676 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6671): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0055 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6667): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0056 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6667): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0057 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6673): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0058 | 0/0 | 6681 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0059 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0060 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0068 | 0/0 | 6680 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0070 | 0/0 | 6684 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0071 | 0/0 | 6676 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6671): Show |
chr2 | 86101235 | 86147157 |
a0001c0001t0072 | 0/0 | 6680 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0001c0003t0008 | 0/0 | 6679 | 9 | 6 | 1 | 0 | 0 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0001c0003t0019 | 0/0 | 6678 | 4 | 3 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6673): Show |
chr2 | 86101235 | 86147157 |
a0001c0003t0027 | 0/0 | 6678 | 3 | 0 | 2 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6673): Show |
chr2 | 86101235 | 86147157 |
a0001c0003t0062 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0001c0003t0063 | 0/0 | 6680 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0001c0006t0066 | 0/0 | 6680 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0001c0006t0067 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0004 | 0/0 | 6679 | 25 | 0 | 0 | 24 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0007 | 0/0 | 6680 | 11 | 0 | 0 | 11 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0020 | 0/0 | 6680 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0022 | 0/0 | 6678 | 4 | 0 | 0 | 2 | 0 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6673): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0061 | 0/0 | 6679 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0064 | 0/0 | 6680 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0002c0002t0065 | 0/0 | 6679 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0002c0005t0026 | 0/0 | 6680 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0003c0004t0006 | 0/0 | 6679 | 12 | 12 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0003c0004t0034 | 0/0 | 6680 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
a0003c0004t0046 | 0/0 | 6679 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6674): Show |
chr2 | 86101235 | 86147157 |
a0004c0009t0001 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0005c0007t0010 | 0/0 | 6684 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6679): Show |
chr2 | 86101235 | 86147157 |
a0006c0011t0001 | 0/0 | 6681 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6676): Show |
chr2 | 86101235 | 86147157 |
a0007c0010t0002 | 0/0 | 6683 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6678): Show |
chr2 | 86101235 | 86147157 |
a0008c0008t0069 | 0/0 | 6680 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | AGAGA others(6675): Show |
chr2 | 86101235 | 86147157 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 0 | 1 | 13 | 0 | 3 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0002 | 0/0 | 10 | 0 | 6 | 2 | 0 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0004 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0005 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0016 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0017 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0009g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0009g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0010g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0011g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0013g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0013g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0014g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0014g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0016g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0017g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0017g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0017g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0018g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0021g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0021g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0023g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0023g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0023g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0024g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0024g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0025g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0025g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0025g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0028g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0028g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0028g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0029g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0030g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0030g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0031g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0032g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0032g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0033g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0033g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0035g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0035g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0036g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0037g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0038g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0039g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0040g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0041g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0042g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0043g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0044g0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0045g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0047g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0048g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0049g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0051g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0052g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0053g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0054g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0055g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0056g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0057g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0058g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0059g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0060g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0068g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0070g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0071g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0001t0072g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0019g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0019g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0027g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0027g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0062g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0003t0063g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0006t0066g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0001c0006t0067g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0007g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0007g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0020g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0020g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0020g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0022g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0022g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0022g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0061g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0064g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0002t0065g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0005t0026g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0005t0026g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0002c0005t0026g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0003c0004t0006g0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0003c0004t0006g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0003c0004t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0003c0004t0034g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0003c0004t0034g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0003c0004t0046g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0004c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0005c0007t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0006c0011t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0007c0010t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
a0008c0008t0069g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0039 | g0179 | EUR | GBR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | GBR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | FIN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00423 | hp1 | a0002 | c0002 | t0004 | g0046 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00438 | hp1 | a0002 | c0002 | t0004 | g0044 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00544 | hp1 | a0001 | c0001 | t0035 | g0003 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0164 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00673 | hp1 | a0002 | c0002 | t0007 | g0012 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | CHS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00733 | hp2 | a0001 | c0001 | t0021 | g0022 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01070 | hp2 | a0001 | c0003 | t0027 | g0211 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01071 | hp1 | a0001 | c0003 | t0027 | g0048 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0172 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01074 | hp2 | a0001 | c0001 | t0021 | g0022 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01106 | hp2 | a0001 | c0001 | t0013 | g0013 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01109 | hp2 | a0001 | c0001 | t0029 | g0009 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01167 | hp1 | a0001 | c0001 | t0025 | g0142 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0146 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0126 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01175 | hp2 | a0001 | c0001 | t0013 | g0085 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01243 | hp1 | a0001 | c0003 | t0008 | g0190 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01243 | hp2 | a0001 | c0001 | t0021 | g0022 | AMR | PUR | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01257 | hp2 | a0001 | c0001 | t0030 | g0087 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01261 | hp2 | a0001 | c0001 | t0017 | g0134 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01358 | hp2 | a0001 | c0001 | t0016 | g0009 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0220 | EUR | IBS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0137 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0178 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0181 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01928 | hp1 | a0001 | c0001 | t0014 | g0042 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01934 | hp1 | a0001 | c0003 | t0019 | g0185 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01981 | hp2 | a0001 | c0001 | t0014 | g0163 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01993 | hp2 | a0001 | c0001 | t0014 | g0042 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02004 | hp2 | a0001 | c0001 | t0030 | g0088 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02015 | hp1 | a0001 | c0001 | t0059 | g0066 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02027 | hp1 | a0002 | c0002 | t0007 | g0049 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0091 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02055 | hp1 | a0003 | c0004 | t0006 | g0233 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02055 | hp2 | a0001 | c0001 | t0017 | g0133 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02080 | hp1 | a0002 | c0002 | t0020 | g0195 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02129 | hp2 | a0002 | c0002 | t0004 | g0011 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02132 | hp1 | a0001 | c0001 | t0031 | g0021 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02135 | hp1 | a0002 | c0002 | t0007 | g0049 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02135 | hp2 | a0004 | c0009 | t0001 | g0001 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02145 | hp1 | a0001 | c0001 | t0051 | g0041 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02145 | hp2 | a0003 | c0004 | t0006 | g0029 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02165 | hp2 | a0001 | c0001 | t0038 | g0168 | EAS | CDX | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02257 | hp1 | a0001 | c0003 | t0008 | g0026 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02257 | hp2 | a0001 | c0001 | t0024 | g0132 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02258 | hp1 | a0001 | c0001 | t0036 | g0015 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02280 | hp1 | a0001 | c0001 | t0023 | g0160 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02280 | hp2 | a0001 | c0003 | t0019 | g0184 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0138 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02523 | hp2 | a0002 | c0002 | t0022 | g0011 | EAS | KHV | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02572 | hp1 | a0001 | c0001 | t0016 | g0009 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02572 | hp2 | a0001 | c0003 | t0063 | g0188 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02602 | hp1 | a0001 | c0001 | t0011 | g0007 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02602 | hp2 | a0001 | c0001 | t0021 | g0008 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02615 | hp1 | a0003 | c0004 | t0006 | g0029 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02615 | hp2 | a0005 | c0007 | t0010 | g0236 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02622 | hp1 | a0003 | c0004 | t0006 | g0006 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02622 | hp2 | a0001 | c0003 | t0062 | g0193 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0173 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02717 | hp1 | a0001 | c0001 | t0016 | g0009 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02717 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02723 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02735 | hp1 | a0001 | c0003 | t0008 | g0186 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02735 | hp2 | a0006 | c0011 | t0001 | g0073 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02738 | hp1 | a0002 | c0002 | t0022 | g0011 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02809 | hp1 | a0001 | c0001 | t0017 | g0040 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02809 | hp2 | a0001 | c0001 | t0023 | g0159 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02818 | hp1 | a0001 | c0001 | t0017 | g0040 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02818 | hp2 | a0001 | c0006 | t0066 | g0051 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02895 | hp1 | a0001 | c0003 | t0008 | g0192 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02897 | hp1 | a0001 | c0003 | t0008 | g0191 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02897 | hp2 | a0001 | c0001 | t0018 | g0103 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02922 | hp1 | a0001 | c0001 | t0028 | g0149 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02965 | hp1 | a0001 | c0001 | t0023 | g0180 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02965 | hp2 | a0003 | c0004 | t0034 | g0234 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0162 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02970 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02976 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02976 | hp2 | a0001 | c0001 | t0028 | g0147 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0158 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0176 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03130 | hp1 | a0001 | c0001 | t0040 | g0043 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03139 | hp1 | a0001 | c0001 | t0025 | g0141 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03209 | hp1 | a0001 | c0003 | t0008 | g0026 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03209 | hp2 | a0001 | c0001 | t0018 | g0024 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03225 | hp1 | a0001 | c0006 | t0067 | g0052 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03239 | hp2 | a0001 | c0001 | t0058 | g0077 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0239 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03453 | hp2 | a0003 | c0004 | t0046 | g0235 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03486 | hp1 | a0001 | c0001 | t0028 | g0148 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03486 | hp2 | a0001 | c0001 | t0071 | g0015 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03516 | hp1 | a0001 | c0001 | t0056 | g0102 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | ESN | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03540 | hp1 | a0001 | c0001 | t0016 | g0009 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03540 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | GWD | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03579 | hp1 | a0001 | c0001 | t0025 | g0143 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03579 | hp2 | a0001 | c0003 | t0008 | g0183 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03654 | hp2 | a0001 | c0001 | t0037 | g0170 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03669 | hp2 | a0001 | c0001 | t0010 | g0113 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03831 | hp2 | a0001 | c0001 | t0010 | g0120 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03834 | hp2 | a0002 | c0002 | t0022 | g0047 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04115 | hp2 | a0002 | c0002 | t0064 | g0213 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0161 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04204 | hp1 | a0002 | c0002 | t0004 | g0212 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG04228 | hp2 | a0001 | c0003 | t0008 | g0187 | SAS | STU | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18522 | hp1 | a0003 | c0004 | t0006 | g0006 | AFR | YRI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0140 | AFR | YRI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18747 | hp1 | a0002 | c0002 | t0007 | g0012 | EAS | CHB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18906 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | YRI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18906 | hp2 | a0001 | c0001 | t0029 | g0009 | AFR | YRI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18939 | hp1 | a0001 | c0001 | t0009 | g0145 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18939 | hp2 | a0002 | c0002 | t0004 | g0197 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18940 | hp1 | a0001 | c0001 | t0011 | g0112 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18940 | hp2 | a0001 | c0001 | t0032 | g0063 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18942 | hp2 | a0002 | c0002 | t0007 | g0012 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18943 | hp2 | a0002 | c0002 | t0061 | g0198 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18944 | hp2 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18945 | hp1 | a0002 | c0002 | t0007 | g0012 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18951 | hp1 | a0001 | c0001 | t0009 | g0035 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18952 | hp1 | a0002 | c0002 | t0004 | g0046 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18953 | hp1 | a0001 | c0001 | t0042 | g0167 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18953 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18954 | hp2 | a0002 | c0002 | t0004 | g0027 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18956 | hp1 | a0002 | c0002 | t0004 | g0207 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18957 | hp1 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18957 | hp2 | a0002 | c0002 | t0065 | g0012 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18959 | hp1 | a0001 | c0001 | t0060 | g0014 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18960 | hp2 | a0002 | c0002 | t0004 | g0200 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18963 | hp2 | a0002 | c0002 | t0007 | g0012 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18965 | hp2 | a0002 | c0005 | t0026 | g0226 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18967 | hp2 | a0002 | c0002 | t0004 | g0209 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18968 | hp2 | a0002 | c0005 | t0026 | g0227 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18969 | hp1 | a0001 | c0001 | t0032 | g0008 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18969 | hp2 | a0001 | c0001 | t0011 | g0119 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18971 | hp1 | a0002 | c0002 | t0007 | g0229 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18974 | hp1 | a0001 | c0001 | t0033 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18977 | hp2 | a0002 | c0002 | t0004 | g0208 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18978 | hp2 | a0001 | c0001 | t0035 | g0223 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18979 | hp2 | a0001 | c0001 | t0068 | g0028 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18981 | hp1 | a0001 | c0001 | t0070 | g0115 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18981 | hp2 | a0001 | c0001 | t0057 | g0030 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18987 | hp2 | a0001 | c0001 | t0013 | g0057 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18989 | hp1 | a0002 | c0002 | t0007 | g0215 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18989 | hp2 | a0002 | c0002 | t0004 | g0206 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18990 | hp2 | a0002 | c0002 | t0020 | g0011 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19001 | hp1 | a0002 | c0002 | t0022 | g0027 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19002 | hp2 | a0002 | c0002 | t0004 | g0204 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19003 | hp2 | a0002 | c0002 | t0004 | g0205 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19004 | hp2 | a0001 | c0001 | t0009 | g0035 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19011 | hp1 | a0002 | c0002 | t0004 | g0027 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19012 | hp1 | a0007 | c0010 | t0002 | g0108 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19012 | hp2 | a0002 | c0002 | t0004 | g0203 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19030 | hp1 | a0001 | c0001 | t0054 | g0144 | AFR | LWK | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19030 | hp2 | a0008 | c0008 | t0069 | g0194 | AFR | LWK | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19043 | hp1 | a0001 | c0001 | t0045 | g0104 | AFR | LWK | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19043 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | LWK | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19055 | hp1 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19055 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19058 | hp1 | a0001 | c0001 | t0009 | g0094 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19058 | hp2 | a0002 | c0005 | t0026 | g0224 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19067 | hp1 | a0001 | c0001 | t0072 | g0105 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19067 | hp2 | a0002 | c0002 | t0020 | g0045 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19068 | hp1 | a0002 | c0002 | t0020 | g0011 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19072 | hp1 | a0001 | c0001 | t0033 | g0232 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19072 | hp2 | a0002 | c0002 | t0004 | g0210 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19074 | hp1 | a0002 | c0002 | t0004 | g0196 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19078 | hp1 | a0001 | c0001 | t0048 | g0109 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19080 | hp1 | a0002 | c0002 | t0004 | g0202 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19082 | hp1 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19087 | hp1 | a0001 | c0001 | t0050 | g0005 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19088 | hp2 | a0002 | c0002 | t0004 | g0199 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19089 | hp2 | a0002 | c0002 | t0007 | g0231 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19090 | hp1 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19091 | hp2 | a0002 | c0002 | t0007 | g0214 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19240 | hp1 | a0001 | c0001 | t0036 | g0015 | AFR | YRI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0024 | AFR | YRI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20129 | hp1 | a0001 | c0001 | t0024 | g0135 | AFR | ASW | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20129 | hp2 | a0001 | c0001 | t0055 | g0100 | AFR | ASW | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20752 | hp2 | a0001 | c0003 | t0027 | g0048 | EUR | TSI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | TSI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | TSI | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01123 | hp1 | a0001 | c0001 | t0049 | g0041 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02109 | hp1 | a0001 | c0001 | t0024 | g0015 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02109 | hp2 | a0003 | c0004 | t0034 | g0029 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02486 | hp1 | a0001 | c0001 | t0053 | g0101 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0039 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02559 | hp1 | a0001 | c0001 | t0043 | g0171 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG02559 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | ACB | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03471 | hp1 | a0001 | c0003 | t0008 | g0189 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG06807 | hp1 | a0001 | c0003 | t0019 | g0026 | AFR | USA | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
HG06807 | hp2 | a0003 | c0004 | t0006 | g0006 | AFR | USA | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18955 | hp1 | a0002 | c0002 | t0004 | g0201 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | USA | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA20300 | hp2 | a0001 | c0003 | t0019 | g0182 | AFR | USA | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA21309 | hp1 | a0001 | c0001 | t0052 | g0015 | AFR | LWK | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
NA21309 | hp2 | a0001 | c0001 | t0041 | g0177 | AFR | LWK | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
homoSapiens | chm13v2 | a0001 | c0001 | t0047 | g0131 | REF | REF | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
homoSapiens | grch38p0 | a0001 | c0001 | t0044 | g0010 | REF | REF | PTCD3_chr2_86101235_86147157 | PTCD3 | chr2 | 86101235 | 86147157 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86106252 | C | T | 1 | a0003 | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
missense_variant | MODERATE | c.5C>T | p.Ala2Val | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/24 | 18/6681 | 5/2070 | 2/689 | chr2 | 86106252 | |||
chr2:86116533 | A | G | 1 | a0006 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.244A>G | p.Thr82Ala | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/24 | 257/6681 | 244/2070 | 82/689 | chr2 | 86116533 | |||
chr2:86118996 | A | G | 1 | a0007 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.490A>G | p.Arg164Gly | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/24 | 503/6681 | 490/2070 | 164/689 | chr2 | 86118996 | |||
chr2:86127228 | A | G | 1 | a0004 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1019A>G | p.Lys340Arg | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 13/24 | 1032/6681 | 1019/2070 | 340/689 | chr2 | 86127228 | |||
chr2:86130651 | A | G | 1 | a0008 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1151A>G | p.Asp384Gly | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/24 | 1164/6681 | 1151/2070 | 384/689 | chr2 | 86130651 | |||
chr2:86134873 | T | C | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1664T>C | p.Ile555Thr | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/24 | 1677/6681 | 1664/2070 | 555/689 | chr2 | 86134873 | |||
chr2:86137530 | A | G | 1 | a0002 | 50 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(47): Show |
missense_variant | MODERATE | c.2041A>G | p.Ser681Gly | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2054/6681 | 2041/2070 | 681/689 | chr2 | 86137530 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86106253 | G | T | 1 | a0001c0006 | 2 | HG02818.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.6G>T | p.Ala2Ala | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/24 | 19/6681 | 6/2070 | 2/689 | chr2 | 86106253 | |||
chr2:86111125 | C | T | 1 | a0001c0006 | 2 | HG02818.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.207C>T | p.Ala69Ala | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/24 | 220/6681 | 207/2070 | 69/689 | chr2 | 86111125 | |||
chr2:86117114 | A | G | 2 | a0001c0003 a0002c0002 |
65 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(62): Show |
synonymous_variant | LOW | c.369A>G | p.Ser123Ser | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/24 | 382/6681 | 369/2070 | 123/689 | chr2 | 86117114 | |||
chr2:86133417 | G | C | 1 | a0008c0008 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1524G>C | p.Val508Val | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/24 | 1537/6681 | 1524/2070 | 508/689 | chr2 | 86133417 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86137583 | TG | T | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
359 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(356): Show |
3_prime_UTR_variant | MODIFIER | c.*27delG | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 27 | INFO_REALIGN_3_PRIME | chr2 | 86137583 | |||||
chr2:86137590 | C | T | 1 | a0001c0001t0072 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 31 | chr2 | 86137590 | ||||||
chr2:86137717 | T | C | 1 | a0001c0001t0045 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 158 | chr2 | 86137717 | ||||||
chr2:86137794 | T | C | 1 | a0003c0004t0046 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*235T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 235 | chr2 | 86137794 | ||||||
chr2:86137971 | A | G | 2 | a0001c0001t0036 a0001c0001t0071 |
3 | HG02258.hp1 HG03486.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*412A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 412 | chr2 | 86137971 | ||||||
chr2:86138297 | ACAT | A | 1 | a0001c0001t0028 | 3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*742_*744delCAT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 742 | INFO_REALIGN_3_PRIME | chr2 | 86138297 | |||||
chr2:86138403 | A | G | 1 | a0001c0001t0070 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 844 | chr2 | 86138403 | ||||||
chr2:86138470 | G | T | 1 | a0001c0001t0028 | 3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*911G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 911 | chr2 | 86138470 | ||||||
chr2:86138484 | T | C | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(8): Show |
75 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*925T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 925 | chr2 | 86138484 | ||||||
chr2:86138590 | G | A | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(35): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*1031G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1031 | chr2 | 86138590 | ||||||
chr2:86138647 | G | C | 15 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0017 others(12): Show |
34 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1088G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1088 | chr2 | 86138647 | ||||||
chr2:86138676 | C | CA | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(44): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*1130dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1131 | INFO_REALIGN_3_PRIME | chr2 | 86138676 | |||||
chr2:86138761 | G | A | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(35): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*1202G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1202 | chr2 | 86138761 | ||||||
chr2:86139374 | T | G | 1 | a0002c0002t0061 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1815T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1815 | chr2 | 86139374 | ||||||
chr2:86139399 | T | A | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(48): Show |
293 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*1840T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1840 | chr2 | 86139399 | ||||||
chr2:86139449 | T | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(42): Show |
243 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*1890T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1890 | chr2 | 86139449 | ||||||
chr2:86139486 | C | A | 1 | a0001c0001t0038 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1927 | chr2 | 86139486 | ||||||
chr2:86139536 | A | AGT | 2 | a0001c0001t0028 a0008c0008t0069 |
4 | HG02922.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1979_*1980dupTG | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 1981 | INFO_REALIGN_3_PRIME | chr2 | 86139536 | |||||
chr2:86139599 | TTGAGACC others(14): Show |
T | 1 | a0001c0001t0023 | 3 | HG02280.hp1 HG02809.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2048_*2068delAGCC others(17): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2048 | INFO_REALIGN_3_PRIME | chr2 | 86139599 | |||||
chr2:86139774 | C | T | 1 | a0001c0001t0060 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2215C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2215 | chr2 | 86139774 | ||||||
chr2:86139787 | T | G | 1 | a0001c0001t0030 | 2 | HG01257.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2228T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2228 | chr2 | 86139787 | ||||||
chr2:86139910 | C | T | 15 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0017 others(12): Show |
34 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2351C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2351 | chr2 | 86139910 | ||||||
chr2:86139993 | G | A | 2 | a0001c0001t0016 a0001c0001t0029 |
6 | HG01109.hp2 HG01358.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2434G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2434 | chr2 | 86139993 | ||||||
chr2:86139993 | G | C | 1 | a0001c0001t0039 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2434G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2434 | chr2 | 86139993 | ||||||
chr2:86140102 | A | G | 2 | a0001c0001t0028 a0008c0008t0069 |
4 | HG02922.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2543 | chr2 | 86140102 | ||||||
chr2:86140206 | C | G | 2 | a0001c0006t0066 a0001c0006t0067 |
2 | HG02818.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2647C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2647 | chr2 | 86140206 | ||||||
chr2:86140227 | C | CA | 6 | a0001c0001t0010 a0001c0001t0033 a0001c0001t0048 others(3): Show |
11 | HG01168.hp2 HG01169.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2687dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2688 | INFO_REALIGN_3_PRIME | chr2 | 86140227 | |||||
chr2:86140227 | CA | C | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(36): Show |
252 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*2687delA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2687 | INFO_REALIGN_3_PRIME | chr2 | 86140227 | |||||
chr2:86140227 | CAA | C | 15 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0017 others(12): Show |
43 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2686_*2687delAA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 2686 | INFO_REALIGN_3_PRIME | chr2 | 86140227 | |||||
chr2:86140618 | C | G | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(54): Show |
304 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*3059C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3059 | chr2 | 86140618 | ||||||
chr2:86140836 | C | T | 1 | a0001c0001t0043 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3277C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3277 | chr2 | 86140836 | ||||||
chr2:86140918 | A | C | 1 | a0001c0001t0068 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3359A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3359 | chr2 | 86140918 | ||||||
chr2:86140919 | A | AAAAC | 18 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0012 others(15): Show |
49 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3361_*3364dupAAAC | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3365 | INFO_REALIGN_3_PRIME | chr2 | 86140919 | |||||
chr2:86140919 | A | AAAC | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(17): Show |
179 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*3362_*3363insCAA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3363 | INFO_REALIGN_3_PRIME | chr2 | 86140919 | |||||
chr2:86140919 | A | AC | 4 | a0001c0003t0008 a0001c0003t0062 a0001c0003t0063 others(1): Show |
12 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3360_*3361insC | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3361 | chr2 | 86140919 | ||||||
chr2:86140919 | A | C | 20 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0015 others(17): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3360A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3360 | chr2 | 86140919 | ||||||
chr2:86141018 | G | A | 1 | a0001c0001t0040 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3459G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3459 | chr2 | 86141018 | ||||||
chr2:86141051 | CAG | C | 4 | a0001c0001t0006 a0003c0004t0006 a0003c0004t0034 others(1): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3494_*3495delGA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3494 | INFO_REALIGN_3_PRIME | chr2 | 86141051 | |||||
chr2:86141069 | C | T | 1 | a0001c0001t0042 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3510C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3510 | chr2 | 86141069 | ||||||
chr2:86141145 | A | C | 5 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0029 others(2): Show |
12 | HG01109.hp2 HG01358.hp2 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3586A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3586 | chr2 | 86141145 | ||||||
chr2:86141229 | G | A | 1 | a0008c0008t0069 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3670G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3670 | chr2 | 86141229 | ||||||
chr2:86141247 | C | T | 5 | a0002c0002t0004 a0002c0002t0020 a0002c0002t0022 others(2): Show |
35 | HG00423.hp1 HG00438.hp1 HG02080.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3688C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3688 | chr2 | 86141247 | ||||||
chr2:86141269 | C | T | 10 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0033 others(7): Show |
68 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3710C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3710 | chr2 | 86141269 | ||||||
chr2:86141386 | G | A | 2 | a0001c0001t0049 a0001c0001t0051 |
2 | HG01123.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3827G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3827 | chr2 | 86141386 | ||||||
chr2:86141427 | C | G | 1 | a0001c0001t0050 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3868C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3868 | chr2 | 86141427 | ||||||
chr2:86141448 | A | G | 1 | a0001c0001t0059 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3889 | chr2 | 86141448 | ||||||
chr2:86141518 | C | A | 7 | a0001c0001t0003 a0001c0001t0033 a0001c0001t0035 others(4): Show |
55 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3959C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 3959 | chr2 | 86141518 | ||||||
chr2:86141560 | A | G | 1 | a0001c0001t0024 | 3 | HG02109.hp1 HG02257.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4001A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4001 | chr2 | 86141560 | ||||||
chr2:86141677 | G | A | 9 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0024 others(6): Show |
19 | HG01109.hp2 HG01261.hp2 HG01358.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4118G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4118 | chr2 | 86141677 | ||||||
chr2:86141681 | G | A | 11 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(8): Show |
114 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*4122G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4122 | chr2 | 86141681 | ||||||
chr2:86141732 | AGAAGT | A | 15 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0017 others(12): Show |
34 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4176_*4180delAGTG others(1): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4176 | INFO_REALIGN_3_PRIME | chr2 | 86141732 | |||||
chr2:86141863 | C | T | 1 | a0001c0001t0041 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4304C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4304 | chr2 | 86141863 | ||||||
chr2:86141931 | C | T | 1 | a0001c0001t0058 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4372C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4372 | chr2 | 86141931 | ||||||
chr2:86141950 | T | TA | 4 | a0001c0001t0006 a0003c0004t0006 a0003c0004t0034 others(1): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4392dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4393 | INFO_REALIGN_3_PRIME | chr2 | 86141950 | |||||
chr2:86142057 | AG | A | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(47): Show |
282 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*4504delG | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 24/24 | 4504 | INFO_REALIGN_3_PRIME | chr2 | 86142057 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86106632 | G | C | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.104+281G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106632 | |||||||
chr2:86106640 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.104+289A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106640 | |||||||
chr2:86106676 | A | G | 1 | a0001c0001t0015g0239 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.104+325A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106676 | |||||||
chr2:86106682 | C | G | 1 | a0001c0001t0003g0238 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.104+331C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106682 | |||||||
chr2:86106757 | C | G | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.104+406C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106757 | |||||||
chr2:86106758 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.104+407G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106758 | |||||||
chr2:86106759 | T | G | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.104+408T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106759 | |||||||
chr2:86106799 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.104+448G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106799 | |||||||
chr2:86106869 | C | T | 2 | a0001c0001t0002g0016 a0005c0007t0010g0236 |
6 | HG00639.hp1 HG01346.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+518C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106869 | |||||||
chr2:86106899 | C | A | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.104+548C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106899 | |||||||
chr2:86106900 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.104+549A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106900 | |||||||
chr2:86106980 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.104+629T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86106980 | |||||||
chr2:86107076 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(149): Show |
234 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.104+725G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107076 | |||||||
chr2:86107091 | T | A | 1 | a0001c0001t0005g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.104+740T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107091 | |||||||
chr2:86107188 | C | T | 7 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 others(4): Show |
7 | NA18972.hp2 NA18978.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+837C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107188 | |||||||
chr2:86107192 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.104+841C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107192 | |||||||
chr2:86107246 | A | G | 6 | a0003c0004t0006g0006 a0003c0004t0006g0029 a0003c0004t0006g0233 others(3): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.104+895A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107246 | |||||||
chr2:86107263 | A | G | 32 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(29): Show |
55 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.104+912A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107263 | |||||||
chr2:86107443 | G | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(234): Show |
359 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(356): Show |
intron_variant | MODIFIER | c.105-907G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107443 | |||||||
chr2:86107789 | C | A | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.105-561C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107789 | |||||||
chr2:86107826 | C | T | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.105-524C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107826 | |||||||
chr2:86107929 | C | T | 2 | a0002c0002t0004g0212 a0002c0002t0064g0213 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.105-421C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86107929 | |||||||
chr2:86107965 | C | CA | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.105-381dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 86107965 | ||||||
chr2:86108085 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(160): Show |
246 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.105-265T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86108085 | |||||||
chr2:86108087 | C | G | 1 | a0001c0003t0062g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.105-263C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | chr2 | 86108087 | |||||||
chr2:86108126 | TA | T | 8 | a0001c0001t0003g0230 a0001c0001t0009g0145 a0001c0001t0010g0146 others(5): Show |
8 | HG01168.hp2 HG02615.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-206delA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 86108126 | ||||||
chr2:86108449 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG03704.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.157+47G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 2/23 | chr2 | 86108449 | |||||||
chr2:86108566 | A | G | 2 | a0001c0003t0008g0191 a0001c0003t0008g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194+30A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86108566 | |||||||
chr2:86108595 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(234): Show |
359 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(356): Show |
intron_variant | MODIFIER | c.194+59G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86108595 | |||||||
chr2:86108665 | G | A | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.194+129G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86108665 | |||||||
chr2:86108925 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(70): Show |
120 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.194+389G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86108925 | |||||||
chr2:86108933 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.194+397C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86108933 | |||||||
chr2:86109049 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.194+513G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109049 | |||||||
chr2:86109050 | T | C | 31 | a0001c0003t0027g0048 a0001c0003t0027g0211 a0002c0002t0004g0011 others(28): Show |
38 | HG00423.hp1 HG00438.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.194+514T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109050 | |||||||
chr2:86109092 | T | C | 29 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(26): Show |
35 | HG00423.hp1 HG00438.hp1 HG02080.hp1 others(32): Show |
intron_variant | MODIFIER | c.194+556T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109092 | |||||||
chr2:86109102 | A | C | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+566A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109102 | |||||||
chr2:86109107 | AC | A | 9 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+573delC | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 86109107 | ||||||
chr2:86109133 | C | T | 39 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
71 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.194+597C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109133 | |||||||
chr2:86109232 | C | T | 8 | a0001c0001t0017g0133 a0001c0001t0017g0134 a0001c0001t0024g0015 others(5): Show |
9 | HG01261.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+696C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109232 | |||||||
chr2:86109323 | C | T | 2 | a0001c0001t0049g0041 a0001c0001t0051g0041 |
2 | HG01123.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.194+787C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109323 | |||||||
chr2:86109365 | C | A | 2 | a0001c0001t0016g0009 a0001c0001t0029g0009 |
6 | HG01109.hp2 HG01358.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+829C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109365 | |||||||
chr2:86109406 | C | CA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(161): Show |
247 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.194+883dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 86109406 | ||||||
chr2:86109615 | G | C | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.194+1079G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109615 | |||||||
chr2:86109622 | T | C | 5 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.194+1086T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109622 | |||||||
chr2:86109695 | A | T | 2 | a0001c0003t0027g0048 a0001c0003t0027g0211 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.194+1159A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109695 | |||||||
chr2:86109931 | T | A | 1 | a0001c0001t0055g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.195-1182T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109931 | |||||||
chr2:86109981 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(70): Show |
120 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.195-1132G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86109981 | |||||||
chr2:86110015 | T | C | 1 | a0001c0001t0028g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195-1098T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110015 | |||||||
chr2:86110036 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.195-1077A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110036 | |||||||
chr2:86110232 | C | T | 1 | a0001c0001t0023g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.195-881C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110232 | |||||||
chr2:86110350 | T | G | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.195-763T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110350 | |||||||
chr2:86110351 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.195-762G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110351 | |||||||
chr2:86110445 | A | G | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.195-668A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110445 | |||||||
chr2:86110597 | A | G | 1 | a0001c0001t0006g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195-516A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110597 | |||||||
chr2:86110613 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.195-500A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110613 | |||||||
chr2:86110764 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.195-349T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110764 | |||||||
chr2:86110807 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.195-306T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86110807 | |||||||
chr2:86111112 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.195-1G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 3/23 | chr2 | 86111112 | |||||||
chr2:86111173 | G | T | 1 | a0001c0001t0055g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.240+15G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111173 | |||||||
chr2:86111175 | G | GT | 32 | a0001c0003t0027g0048 a0001c0003t0027g0211 a0002c0002t0004g0011 others(29): Show |
39 | HG00423.hp1 HG00438.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.240+26dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86111175 | ||||||
chr2:86111210 | C | CT | 14 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0008g0186 others(11): Show |
15 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.240+57dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86111210 | ||||||
chr2:86111277 | G | A | 29 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(26): Show |
35 | HG00423.hp1 HG00438.hp1 HG02080.hp1 others(32): Show |
intron_variant | MODIFIER | c.240+119G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111277 | |||||||
chr2:86111349 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.240+191G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111349 | |||||||
chr2:86111350 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.240+192A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111350 | |||||||
chr2:86111429 | A | T | 1 | a0002c0002t0004g0210 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.240+271A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111429 | |||||||
chr2:86111445 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(69): Show |
119 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.240+287A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111445 | |||||||
chr2:86111456 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.240+298C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111456 | |||||||
chr2:86111459 | G | A | 1 | a0001c0001t0023g0159 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.240+301G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111459 | |||||||
chr2:86111566 | C | T | 2 | a0001c0001t0017g0040 a0001c0001t0055g0100 |
3 | HG02809.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.240+408C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111566 | |||||||
chr2:86111735 | G | C | 1 | a0001c0001t0013g0057 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.240+577G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111735 | |||||||
chr2:86111744 | T | C | 29 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(26): Show |
35 | HG00423.hp1 HG00438.hp1 HG02080.hp1 others(32): Show |
intron_variant | MODIFIER | c.240+586T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111744 | |||||||
chr2:86111806 | G | A | 4 | a0001c0001t0018g0024 a0001c0001t0018g0103 a0001c0001t0053g0101 others(1): Show |
6 | HG02486.hp1 HG02897.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+648G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111806 | |||||||
chr2:86111821 | C | T | 2 | a0001c0003t0027g0048 a0001c0003t0027g0211 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+663C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111821 | |||||||
chr2:86111831 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0096 |
3 | NA18972.hp1 NA18988.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.240+673A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111831 | |||||||
chr2:86111939 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.240+781T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111939 | |||||||
chr2:86111939 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.240+781T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111939 | |||||||
chr2:86111940 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.240+782C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111940 | |||||||
chr2:86111941 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.240+783T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86111941 | |||||||
chr2:86112036 | G | A | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.240+878G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112036 | |||||||
chr2:86112042 | C | CT | 12 | a0001c0001t0002g0054 a0001c0001t0003g0003 a0001c0001t0003g0019 others(9): Show |
22 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.240+904dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112042 | ||||||
chr2:86112042 | CT | C | 37 | a0001c0001t0001g0060 a0001c0001t0001g0237 a0001c0001t0003g0230 others(34): Show |
44 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.240+904delT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112042 | ||||||
chr2:86112046 | T | TC | 2 | a0001c0003t0027g0048 a0001c0003t0027g0211 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.240+888_240+889ins others(1): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112046 | |||||||
chr2:86112096 | G | A | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.240+938G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112096 | |||||||
chr2:86112125 | C | G | 11 | a0001c0001t0003g0018 a0001c0001t0003g0028 a0001c0001t0003g0222 others(8): Show |
15 | NA18948.hp1 NA18965.hp2 NA18968.hp2 others(12): Show |
intron_variant | MODIFIER | c.240+967C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112125 | |||||||
chr2:86112208 | C | T | 48 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
75 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.240+1050C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112208 | |||||||
chr2:86112246 | C | T | 9 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+1088C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112246 | |||||||
chr2:86112327 | A | G | 2 | a0001c0003t0008g0191 a0001c0003t0008g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.240+1169A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112327 | |||||||
chr2:86112351 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(31): Show |
58 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.240+1193C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112351 | |||||||
chr2:86112355 | C | CT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(93): Show |
145 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.240+1213dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112355 | ||||||
chr2:86112375 | A | C | 2 | a0001c0001t0016g0009 a0001c0001t0029g0009 |
6 | HG01109.hp2 HG01358.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+1217A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112375 | |||||||
chr2:86112378 | A | G | 9 | a0001c0003t0008g0186 a0001c0003t0008g0187 a0001c0003t0008g0189 others(6): Show |
9 | HG01243.hp1 HG01934.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+1220A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112378 | |||||||
chr2:86112411 | GTAATCCC others(5): Show |
G | 4 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(1): Show |
4 | NA18972.hp2 NA19006.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+1267_240+1278d others(14): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112411 | ||||||
chr2:86112461 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.240+1303G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112461 | |||||||
chr2:86112542 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.240+1384G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112542 | |||||||
chr2:86112642 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.240+1484A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112642 | |||||||
chr2:86112681 | C | CA | 36 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(33): Show |
62 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.240+1546dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112681 | ||||||
chr2:86112681 | C | CAA | 44 | a0001c0001t0003g0222 a0001c0001t0006g0181 a0001c0003t0008g0026 others(41): Show |
56 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.240+1545_240+1546d others(4): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112681 | ||||||
chr2:86112681 | C | CAAA | 5 | a0001c0003t0027g0048 a0001c0003t0027g0211 a0002c0002t0004g0196 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+1544_240+1546d others(5): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112681 | ||||||
chr2:86112681 | CA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(108): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.240+1546delA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112681 | ||||||
chr2:86112681 | CAA | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
12 | HG00323.hp2 HG01169.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+1545_240+1546d others(4): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86112681 | ||||||
chr2:86112721 | C | A | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.240+1563C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112721 | |||||||
chr2:86112726 | C | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0065 others(4): Show |
10 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+1568C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112726 | |||||||
chr2:86112806 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.240+1648C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112806 | |||||||
chr2:86112828 | C | T | 1 | a0001c0001t0013g0091 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.240+1670C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112828 | |||||||
chr2:86112944 | A | T | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.240+1786A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86112944 | |||||||
chr2:86113081 | T | A | 1 | a0001c0001t0059g0066 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.240+1923T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113081 | |||||||
chr2:86113087 | G | A | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.240+1929G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113087 | |||||||
chr2:86113101 | G | A | 17 | a0001c0001t0016g0009 a0001c0001t0017g0040 a0001c0001t0017g0133 others(14): Show |
25 | HG01109.hp2 HG01261.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.240+1943G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113101 | |||||||
chr2:86113152 | C | T | 1 | a0001c0001t0012g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.240+1994C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113152 | |||||||
chr2:86113377 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.240+2219C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113377 | |||||||
chr2:86113490 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(197): Show |
294 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.240+2332G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113490 | |||||||
chr2:86113566 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.240+2408G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113566 | |||||||
chr2:86113596 | G | A | 1 | a0001c0001t0015g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.240+2438G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113596 | |||||||
chr2:86113667 | C | T | 9 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+2509C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113667 | |||||||
chr2:86113668 | G | A | 36 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(33): Show |
47 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.240+2510G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113668 | |||||||
chr2:86113802 | C | A | 2 | a0001c0001t0014g0042 a0001c0001t0014g0163 |
3 | HG01928.hp1 HG01981.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.240+2644C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113802 | |||||||
chr2:86113821 | T | A | 1 | a0001c0001t0013g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.240+2663T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86113821 | |||||||
chr2:86114021 | CAATGAG | C | 26 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(23): Show |
34 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.241-2504_241-2499d others(8): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 86114021 | ||||||
chr2:86114133 | CA | C | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0129 |
3 | HG00323.hp2 HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.241-2396delA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114133 | |||||||
chr2:86114136 | C | G | 1 | a0001c0001t0054g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241-2394C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114136 | |||||||
chr2:86114205 | G | A | 46 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(43): Show |
69 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.241-2325G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114205 | |||||||
chr2:86114303 | A | G | 1 | a0001c0001t0015g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.241-2227A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114303 | |||||||
chr2:86114433 | G | A | 1 | a0001c0001t0033g0232 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241-2097G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114433 | |||||||
chr2:86114509 | T | G | 2 | a0001c0003t0008g0191 a0001c0003t0008g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.241-2021T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114509 | |||||||
chr2:86114679 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.241-1851T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114679 | |||||||
chr2:86114761 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.241-1769G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114761 | |||||||
chr2:86114802 | C | T | 1 | a0001c0001t0003g0216 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.241-1728C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114802 | |||||||
chr2:86114974 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.241-1556T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86114974 | |||||||
chr2:86115083 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(120): Show |
197 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.241-1447C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115083 | |||||||
chr2:86115138 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.241-1392G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115138 | |||||||
chr2:86115180 | G | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(29): Show |
59 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.241-1350G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115180 | |||||||
chr2:86115222 | G | A | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.241-1308G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115222 | |||||||
chr2:86115243 | A | C | 25 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(22): Show |
43 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.241-1287A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115243 | |||||||
chr2:86115269 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.241-1261A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115269 | |||||||
chr2:86115501 | T | G | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.241-1029T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115501 | |||||||
chr2:86115666 | A | G | 14 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0008g0186 others(11): Show |
15 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.241-864A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115666 | |||||||
chr2:86115723 | G | C | 5 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(2): Show |
5 | HG00544.hp2 HG02056.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-807G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86115723 | |||||||
chr2:86116136 | T | C | 2 | a0001c0001t0016g0009 a0001c0001t0029g0009 |
6 | HG01109.hp2 HG01358.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-394T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116136 | |||||||
chr2:86116173 | C | T | 1 | a0001c0001t0014g0163 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.241-357C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116173 | |||||||
chr2:86116193 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
73 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.241-337G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116193 | |||||||
chr2:86116284 | C | G | 3 | a0001c0001t0001g0089 a0001c0001t0030g0087 a0001c0001t0030g0088 |
3 | HG01257.hp2 HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.241-246C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116284 | |||||||
chr2:86116353 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.241-177C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116353 | |||||||
chr2:86116371 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(149): Show |
234 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.241-159G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116371 | |||||||
chr2:86116498 | A | G | 1 | a0001c0001t0021g0022 | 3 | HG00733.hp2 HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.241-32A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 4/23 | chr2 | 86116498 | |||||||
chr2:86116645 | C | T | 1 | a0003c0004t0046g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+47C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116645 | |||||||
chr2:86116646 | G | A | 1 | a0001c0001t0002g0037 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.309+48G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116646 | |||||||
chr2:86116704 | A | C | 1 | a0001c0001t0002g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.309+106A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116704 | |||||||
chr2:86116717 | C | T | 36 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(33): Show |
47 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.309+119C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116717 | |||||||
chr2:86116788 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(70): Show |
120 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.309+190G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116788 | |||||||
chr2:86116789 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.309+191G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116789 | |||||||
chr2:86116952 | C | T | 1 | a0001c0001t0013g0091 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.310-103C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116952 | |||||||
chr2:86116957 | G | GT | 19 | a0001c0001t0001g0034 a0001c0001t0001g0086 a0001c0001t0001g0237 others(16): Show |
21 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.310-89dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 86116957 | ||||||
chr2:86116972 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(70): Show |
120 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.310-83G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86116972 | |||||||
chr2:86117029 | G | A | 1 | a0001c0001t0055g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.310-26G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 5/23 | chr2 | 86117029 | |||||||
chr2:86117244 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(236): Show |
361 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(358): Show |
intron_variant | MODIFIER | c.414+85T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86117244 | |||||||
chr2:86117250 | A | G | 1 | a0001c0001t0017g0040 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.414+91A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86117250 | |||||||
chr2:86117287 | G | T | 1 | a0001c0001t0045g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.414+128G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86117287 | |||||||
chr2:86117931 | C | T | 1 | a0002c0002t0004g0206 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.414+772C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86117931 | |||||||
chr2:86117968 | G | A | 26 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(23): Show |
34 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.414+809G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86117968 | |||||||
chr2:86118064 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.415-857C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118064 | |||||||
chr2:86118226 | A | C | 25 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(22): Show |
43 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.415-695A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118226 | |||||||
chr2:86118250 | T | G | 1 | a0001c0001t0005g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.415-671T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118250 | |||||||
chr2:86118298 | T | C | 2 | a0001c0001t0005g0164 a0001c0001t0005g0165 |
2 | HG00544.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.415-623T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118298 | |||||||
chr2:86118412 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.415-509C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118412 | |||||||
chr2:86118413 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(159): Show |
244 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.415-508A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118413 | |||||||
chr2:86118423 | T | C | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.415-498T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118423 | |||||||
chr2:86118483 | TGAG | T | 4 | a0001c0001t0002g0107 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG00323.hp2 HG00642.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-435_415-433del others(3): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 86118483 | ||||||
chr2:86118535 | A | G | 1 | a0001c0001t0010g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.415-386A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118535 | |||||||
chr2:86118688 | C | T | 1 | a0001c0001t0053g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415-233C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118688 | |||||||
chr2:86118753 | T | G | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.415-168T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118753 | |||||||
chr2:86118830 | G | A | 1 | a0001c0001t0037g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415-91G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 6/23 | chr2 | 86118830 | |||||||
chr2:86119057 | G | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(29): Show |
59 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.538+13G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119057 | |||||||
chr2:86119141 | G | C | 1 | a0001c0001t0012g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.538+97G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119141 | |||||||
chr2:86119169 | G | A | 1 | a0001c0001t0043g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.538+125G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119169 | |||||||
chr2:86119172 | C | G | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.538+128C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119172 | |||||||
chr2:86119185 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(234): Show |
359 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(356): Show |
intron_variant | MODIFIER | c.538+141G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119185 | |||||||
chr2:86119207 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.538+163T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119207 | |||||||
chr2:86119339 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.538+295C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119339 | |||||||
chr2:86119360 | C | CT | 7 | a0001c0001t0041g0177 a0002c0002t0004g0027 a0002c0002t0004g0046 others(4): Show |
9 | HG00423.hp1 NA18939.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+330dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 86119360 | ||||||
chr2:86119360 | CT | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(148): Show |
233 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.538+330delT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 86119360 | ||||||
chr2:86119368 | T | A | 2 | a0001c0001t0015g0162 a0001c0001t0015g0178 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.538+324T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119368 | |||||||
chr2:86119394 | T | C | 36 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(33): Show |
47 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.538+350T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119394 | |||||||
chr2:86119645 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.538+601C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119645 | |||||||
chr2:86119717 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.538+673G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86119717 | |||||||
chr2:86120042 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.538+998A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120042 | |||||||
chr2:86120170 | C | A | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.538+1126C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120170 | |||||||
chr2:86120326 | G | T | 2 | a0001c0003t0008g0191 a0001c0003t0008g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.539-1153G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120326 | |||||||
chr2:86120449 | ATTAT | A | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.539-1028_539-1025d others(6): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 86120449 | ||||||
chr2:86120532 | G | T | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.539-947G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120532 | |||||||
chr2:86120665 | CAGG | C | 33 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(30): Show |
44 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.539-809_539-807del others(3): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 86120665 | ||||||
chr2:86120703 | T | A | 1 | a0001c0001t0005g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.539-776T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120703 | |||||||
chr2:86120720 | C | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(202): Show |
300 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.539-759C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120720 | |||||||
chr2:86120865 | C | T | 1 | a0001c0001t0041g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-614C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120865 | |||||||
chr2:86120870 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.539-609C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120870 | |||||||
chr2:86120902 | G | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(22): Show |
43 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.539-577G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120902 | |||||||
chr2:86120905 | A | G | 2 | a0001c0001t0009g0035 a0001c0001t0009g0145 |
3 | NA18939.hp1 NA18951.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.539-574A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120905 | |||||||
chr2:86120908 | T | C | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.539-571T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120908 | |||||||
chr2:86120946 | T | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(70): Show |
120 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.539-533T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86120946 | |||||||
chr2:86121004 | T | C | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.539-475T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86121004 | |||||||
chr2:86121020 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0092 |
3 | HG01346.hp1 HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.539-459T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86121020 | |||||||
chr2:86121029 | A | G | 1 | a0001c0001t0025g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-450A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86121029 | |||||||
chr2:86121038 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.539-441C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86121038 | |||||||
chr2:86121105 | C | T | 26 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(23): Show |
32 | HG00423.hp1 HG00438.hp1 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.539-374C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86121105 | |||||||
chr2:86121109 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.539-370C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 7/23 | chr2 | 86121109 | |||||||
chr2:86121837 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.654+243G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86121837 | |||||||
chr2:86121881 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(202): Show |
300 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.654+287G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86121881 | |||||||
chr2:86121895 | T | C | 9 | a0001c0001t0017g0133 a0001c0001t0017g0134 a0001c0001t0024g0015 others(6): Show |
10 | HG01261.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+301T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86121895 | |||||||
chr2:86122104 | A | G | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.654+510A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122104 | |||||||
chr2:86122268 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.654+674A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122268 | |||||||
chr2:86122272 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.654+678G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122272 | |||||||
chr2:86122367 | T | C | 36 | a0002c0002t0004g0011 a0002c0002t0004g0027 a0002c0002t0004g0044 others(33): Show |
47 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.654+773T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122367 | |||||||
chr2:86122476 | A | G | 5 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+882A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122476 | |||||||
chr2:86122537 | A | C | 1 | a0002c0002t0004g0207 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.654+943A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122537 | |||||||
chr2:86122578 | GT | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.654+992delT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 86122578 | ||||||
chr2:86122637 | G | C | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+1043G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122637 | |||||||
chr2:86122651 | G | A | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.655-1050G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122651 | |||||||
chr2:86122747 | T | C | 14 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0008g0186 others(11): Show |
15 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.655-954T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86122747 | |||||||
chr2:86123055 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.655-646C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123055 | |||||||
chr2:86123090 | C | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(22): Show |
43 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.655-611C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123090 | |||||||
chr2:86123095 | TAA | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(22): Show |
43 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.655-599_655-598del others(2): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 86123095 | ||||||
chr2:86123155 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.655-546C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123155 | |||||||
chr2:86123156 | G | A | 3 | a0001c0001t0005g0158 a0001c0001t0005g0173 a0001c0001t0037g0170 |
3 | HG02683.hp1 HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.655-545G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123156 | |||||||
chr2:86123185 | C | T | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655-516C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123185 | |||||||
chr2:86123261 | T | TA | 34 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(31): Show |
62 | HG00544.hp1 HG00673.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.655-423dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 86123261 | ||||||
chr2:86123261 | TA | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(144): Show |
229 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.655-423delA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 86123261 | ||||||
chr2:86123446 | C | T | 2 | a0001c0003t0027g0048 a0001c0003t0027g0211 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.655-255C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123446 | |||||||
chr2:86123474 | G | A | 38 | a0001c0003t0027g0048 a0001c0003t0027g0211 a0002c0002t0004g0011 others(35): Show |
50 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.655-227G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123474 | |||||||
chr2:86123541 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(118): Show |
195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.655-160A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 8/23 | chr2 | 86123541 | |||||||
chr2:86123921 | G | A | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.716+159G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86123921 | |||||||
chr2:86123924 | T | C | 4 | a0001c0001t0025g0141 a0001c0001t0025g0142 a0001c0001t0025g0143 others(1): Show |
4 | HG01167.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.716+162T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86123924 | |||||||
chr2:86124117 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.716+355T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124117 | |||||||
chr2:86124325 | A | T | 26 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(23): Show |
34 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.716+563A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124325 | |||||||
chr2:86124485 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0010g0039 |
2 | HG00738.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.717-510C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124485 | |||||||
chr2:86124495 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.717-500C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124495 | |||||||
chr2:86124518 | G | A | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.717-477G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124518 | |||||||
chr2:86124561 | G | A | 2 | a0001c0001t0003g0216 a0001c0001t0003g0217 |
2 | HG02056.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.717-434G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124561 | |||||||
chr2:86124628 | C | T | 1 | a0001c0001t0038g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.717-367C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124628 | |||||||
chr2:86124697 | A | T | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.717-298A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124697 | |||||||
chr2:86124699 | A | G | 1 | a0001c0001t0018g0103 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.717-296A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124699 | |||||||
chr2:86124701 | A | C | 12 | a0001c0001t0006g0181 a0001c0003t0008g0026 a0001c0003t0008g0183 others(9): Show |
22 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.717-294A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124701 | |||||||
chr2:86124887 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(190): Show |
282 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.717-108G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124887 | |||||||
chr2:86124914 | A | G | 3 | a0001c0001t0003g0017 a0001c0001t0003g0220 a0001c0001t0003g0221 |
6 | HG01069.hp1 HG01081.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.717-81A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 9/23 | chr2 | 86124914 | |||||||
chr2:86125185 | G | C | 2 | a0001c0003t0027g0048 a0001c0003t0027g0211 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.804+103G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 10/23 | chr2 | 86125185 | |||||||
chr2:86125229 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.804+147A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 10/23 | chr2 | 86125229 | |||||||
chr2:86125244 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.804+162T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 10/23 | chr2 | 86125244 | |||||||
chr2:86125257 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.804+175C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 10/23 | chr2 | 86125257 | |||||||
chr2:86125270 | G | A | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0129 |
3 | HG00323.hp2 HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.805-185G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 10/23 | chr2 | 86125270 | |||||||
chr2:86125662 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(120): Show |
197 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.866-133G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 11/23 | chr2 | 86125662 | |||||||
chr2:86125671 | A | C | 1 | a0001c0001t0005g0165 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.866-124A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 11/23 | chr2 | 86125671 | |||||||
chr2:86125702 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.866-93C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 11/23 | chr2 | 86125702 | |||||||
chr2:86126020 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.951+140A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126020 | |||||||
chr2:86126027 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.951+147G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126027 | |||||||
chr2:86126058 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.951+178G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126058 | |||||||
chr2:86126162 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.951+282G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126162 | |||||||
chr2:86126229 | C | CA | 40 | a0001c0001t0001g0072 a0001c0001t0001g0096 a0001c0001t0002g0038 others(37): Show |
52 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.951+363dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 86126229 | ||||||
chr2:86126243 | AG | A | 13 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0082 others(10): Show |
17 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.951+364delG | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126243 | |||||||
chr2:86126244 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(184): Show |
277 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.951+364G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126244 | |||||||
chr2:86126250 | G | A | 4 | a0001c0001t0018g0024 a0001c0001t0018g0103 a0001c0001t0053g0101 others(1): Show |
6 | HG02486.hp1 HG02897.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+370G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126250 | |||||||
chr2:86126263 | A | G | 1 | a0001c0001t0005g0173 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.951+383A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126263 | |||||||
chr2:86126278 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0110 a0001c0001t0002g0122 others(3): Show |
13 | HG01109.hp1 HG01943.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+398C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126278 | |||||||
chr2:86126337 | C | T | 1 | a0003c0004t0034g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.951+457C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126337 | |||||||
chr2:86126365 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.951+485C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126365 | |||||||
chr2:86126530 | C | T | 1 | a0001c0001t0043g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.952-631C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126530 | |||||||
chr2:86126605 | C | T | 28 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0012g0136 others(25): Show |
36 | HG01109.hp2 HG01167.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.952-556C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126605 | |||||||
chr2:86126663 | C | T | 32 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(29): Show |
59 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.952-498C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126663 | |||||||
chr2:86126763 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0121 a0001c0001t0011g0007 others(2): Show |
11 | HG02083.hp2 HG02602.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.952-398C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126763 | |||||||
chr2:86126831 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(160): Show |
246 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.952-330T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126831 | |||||||
chr2:86126837 | C | CA | 58 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0005g0161 others(55): Show |
71 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.952-309dupA | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 86126837 | ||||||
chr2:86126900 | C | T | 1 | a0001c0001t0054g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.952-261C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86126900 | |||||||
chr2:86127083 | C | A | 1 | a0002c0002t0004g0208 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.952-78C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86127083 | |||||||
chr2:86127117 | A | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0068 a0001c0001t0001g0093 |
4 | HG00735.hp2 HG01433.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-44A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 12/23 | chr2 | 86127117 | |||||||
chr2:86127481 | C | T | 1 | a0001c0001t0070g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1096+176C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 13/23 | chr2 | 86127481 | |||||||
chr2:86127545 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1096+240G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 13/23 | chr2 | 86127545 | |||||||
chr2:86127581 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(160): Show |
246 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1096+276T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 13/23 | chr2 | 86127581 | |||||||
chr2:86127630 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0152 |
2 | NA18978.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1097-311G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 13/23 | chr2 | 86127630 | |||||||
chr2:86127659 | A | G | 2 | a0001c0006t0066g0051 a0001c0006t0067g0052 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1097-282A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 13/23 | chr2 | 86127659 | |||||||
chr2:86128014 | T | C | 5 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0019g0026 others(2): Show |
6 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+23T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128014 | |||||||
chr2:86128188 | T | C | 2 | a0001c0001t0002g0111 a0001c0001t0002g0130 |
2 | HG00099.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1147+197T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128188 | |||||||
chr2:86128262 | A | AT | 72 | a0001c0001t0001g0067 a0001c0001t0001g0237 a0001c0001t0002g0004 others(69): Show |
109 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1147+289dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 86128262 | ||||||
chr2:86128389 | G | T | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1147+398G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128389 | |||||||
chr2:86128432 | T | C | 1 | a0001c0001t0039g0179 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1147+441T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128432 | |||||||
chr2:86128545 | A | G | 6 | a0002c0002t0004g0045 a0002c0002t0004g0196 a0002c0002t0004g0203 others(3): Show |
6 | NA18956.hp1 NA18957.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1147+554A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128545 | |||||||
chr2:86128570 | G | A | 4 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147+579G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128570 | |||||||
chr2:86128605 | A | T | 7 | a0001c0003t0008g0186 a0001c0003t0008g0187 a0001c0003t0008g0189 others(4): Show |
7 | HG01243.hp1 HG01934.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147+614A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128605 | |||||||
chr2:86128736 | C | A | 1 | a0001c0003t0019g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1147+745C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86128736 | |||||||
chr2:86129031 | G | A | 9 | a0001c0003t0008g0186 a0001c0003t0008g0187 a0001c0003t0008g0189 others(6): Show |
9 | HG01243.hp1 HG01934.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1147+1040G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129031 | |||||||
chr2:86129128 | C | G | 1 | a0002c0002t0004g0044 | 2 | HG00438.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1147+1137C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129128 | |||||||
chr2:86129372 | A | G | 1 | a0001c0001t0012g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1148-1276A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129372 | |||||||
chr2:86129392 | G | A | 17 | a0001c0001t0016g0009 a0001c0001t0017g0040 a0001c0001t0017g0133 others(14): Show |
25 | HG01109.hp2 HG01261.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.1148-1256G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129392 | |||||||
chr2:86129643 | A | G | 5 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0138 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148-1005A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129643 | |||||||
chr2:86129789 | A | G | 1 | a0001c0001t0024g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1148-859A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129789 | |||||||
chr2:86129882 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1148-766G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86129882 | |||||||
chr2:86129936 | CATTA | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1148-708_1148-705d others(6): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 86129936 | ||||||
chr2:86130128 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1148-520C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86130128 | |||||||
chr2:86130486 | G | C | 1 | a0001c0001t0005g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1148-162G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86130486 | |||||||
chr2:86130495 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0096 |
3 | NA18972.hp1 NA18988.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1148-153G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 14/23 | chr2 | 86130495 | |||||||
chr2:86130785 | C | T | 2 | a0001c0003t0027g0048 a0001c0003t0027g0211 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1237+48C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/23 | chr2 | 86130785 | |||||||
chr2:86130837 | A | AT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0064 others(9): Show |
21 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1237+115dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr2 | 86130837 | ||||||
chr2:86130837 | A | T | 1 | a0001c0006t0067g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1237+100A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/23 | chr2 | 86130837 | |||||||
chr2:86130837 | AT | A | 53 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(50): Show |
88 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.1237+115delT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr2 | 86130837 | ||||||
chr2:86130852 | T | A | 1 | a0006c0011t0001g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1237+115T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/23 | chr2 | 86130852 | |||||||
chr2:86130979 | A | C | 14 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0008g0186 others(11): Show |
15 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1238-99A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 15/23 | chr2 | 86130979 | |||||||
chr2:86131317 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1266+211T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131317 | |||||||
chr2:86131336 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(144): Show |
229 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1266+230C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131336 | |||||||
chr2:86131437 | A | C | 14 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0008g0186 others(11): Show |
15 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1266+331A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131437 | |||||||
chr2:86131477 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1266+371A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131477 | |||||||
chr2:86131714 | A | C | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1267-604A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131714 | |||||||
chr2:86131876 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1267-442A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131876 | |||||||
chr2:86131963 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(149): Show |
234 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1267-355C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131963 | |||||||
chr2:86131964 | C | T | 1 | a0001c0001t0058g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1267-354C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131964 | |||||||
chr2:86131977 | T | A | 1 | a0001c0001t0025g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1267-341T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86131977 | |||||||
chr2:86132003 | G | A | 1 | a0001c0001t0009g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1267-315G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86132003 | |||||||
chr2:86132093 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(195): Show |
288 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1267-225C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86132093 | |||||||
chr2:86132282 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1267-36G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 16/23 | chr2 | 86132282 | |||||||
chr2:86132445 | T | C | 1 | a0001c0001t0054g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1373+21T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132445 | |||||||
chr2:86132508 | C | T | 1 | a0001c0001t0005g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1373+84C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132508 | |||||||
chr2:86132622 | G | GT | 52 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(49): Show |
76 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1373+217dupT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 86132622 | ||||||
chr2:86132622 | G | GTT | 25 | a0001c0001t0003g0019 a0001c0001t0003g0028 a0001c0001t0003g0217 others(22): Show |
32 | HG00423.hp1 HG00673.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1373+216_1373+217d others(4): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 86132622 | ||||||
chr2:86132622 | GT | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(120): Show |
204 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1373+217delT | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 86132622 | ||||||
chr2:86132622 | GTT | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0090 a0001c0001t0002g0114 others(5): Show |
8 | HG01167.hp1 HG02258.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1373+216_1373+217d others(4): Show |
PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 86132622 | ||||||
chr2:86132625 | T | G | 2 | a0001c0001t0012g0136 a0001c0001t0017g0040 |
3 | HG01891.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1373+201T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132625 | |||||||
chr2:86132626 | T | G | 20 | a0001c0001t0012g0137 a0001c0001t0012g0138 a0001c0001t0012g0139 others(17): Show |
27 | HG01109.hp2 HG01261.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1373+202T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132626 | |||||||
chr2:86132627 | T | G | 4 | a0001c0001t0025g0141 a0001c0001t0025g0142 a0001c0001t0025g0143 others(1): Show |
4 | HG01167.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373+203T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132627 | |||||||
chr2:86132714 | G | T | 1 | a0002c0002t0004g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1373+290G>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132714 | |||||||
chr2:86132716 | T | C | 5 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0019g0026 others(2): Show |
6 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373+292T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132716 | |||||||
chr2:86132830 | T | A | 3 | a0001c0001t0005g0043 a0001c0001t0005g0157 a0001c0001t0040g0043 |
3 | HG02451.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1374-348T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132830 | |||||||
chr2:86132901 | A | G | 5 | a0001c0001t0009g0021 a0001c0001t0009g0035 a0001c0001t0009g0095 others(2): Show |
7 | HG02132.hp1 NA18939.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374-277A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86132901 | |||||||
chr2:86133102 | A | G | 48 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
75 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1374-76A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 17/23 | chr2 | 86133102 | |||||||
chr2:86133309 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1453-37C>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 18/23 | chr2 | 86133309 | |||||||
chr2:86133318 | GC | G | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1453-27delC | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 18/23 | chr2 | 86133318 | |||||||
chr2:86133450 | T | G | 32 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(29): Show |
55 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1543+14T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86133450 | |||||||
chr2:86133587 | C | T | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1543+151C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86133587 | |||||||
chr2:86133686 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1543+250G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86133686 | |||||||
chr2:86133754 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0079 |
2 | NA18951.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1543+318C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86133754 | |||||||
chr2:86133766 | T | C | 1 | a0001c0001t0011g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1543+330T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86133766 | |||||||
chr2:86133793 | C | G | 32 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(29): Show |
59 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1543+357C>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86133793 | |||||||
chr2:86134109 | G | A | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1544-183G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86134109 | |||||||
chr2:86134240 | T | C | 1 | a0001c0001t0025g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1544-52T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 19/23 | chr2 | 86134240 | |||||||
chr2:86135081 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(147): Show |
232 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1778+94C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86135081 | |||||||
chr2:86135148 | T | G | 1 | a0007c0010t0002g0108 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1778+161T>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86135148 | |||||||
chr2:86135193 | C | T | 1 | a0001c0001t0005g0174 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1778+206C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86135193 | |||||||
chr2:86135197 | G | A | 7 | a0001c0001t0006g0181 a0003c0004t0006g0006 a0003c0004t0006g0029 others(4): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1778+210G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86135197 | |||||||
chr2:86135883 | T | C | 1 | a0001c0001t0055g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1779-638T>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86135883 | |||||||
chr2:86135951 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(146): Show |
231 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1779-570A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86135951 | |||||||
chr2:86136031 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1779-490A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86136031 | |||||||
chr2:86136324 | A | G | 1 | a0008c0008t0069g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1779-197A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86136324 | |||||||
chr2:86136496 | A | T | 1 | a0001c0001t0010g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1779-25A>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 21/23 | chr2 | 86136496 | |||||||
chr2:86136686 | C | T | 3 | a0002c0002t0004g0199 a0002c0002t0004g0201 a0002c0002t0004g0209 |
3 | NA18955.hp1 NA18967.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1820+124C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 22/23 | chr2 | 86136686 | |||||||
chr2:86136732 | G | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(232): Show |
357 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(354): Show |
intron_variant | MODIFIER | c.1820+170G>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 22/23 | chr2 | 86136732 | |||||||
chr2:86136932 | G | A | 2 | a0001c0001t0016g0009 a0001c0001t0029g0009 |
6 | HG01109.hp2 HG01358.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1821-50G>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 22/23 | chr2 | 86136932 | |||||||
chr2:86137167 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1979+27T>A | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 23/23 | chr2 | 86137167 | |||||||
chr2:86137230 | A | G | 55 | a0001c0003t0008g0026 a0001c0003t0008g0183 a0001c0003t0008g0186 others(52): Show |
68 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1979+90A>G | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 23/23 | chr2 | 86137230 | |||||||
chr2:86137285 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0070 others(2): Show |
8 | HG00558.hp2 NA18954.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1979+145C>T | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 23/23 | chr2 | 86137285 | |||||||
chr2:86137438 | A | C | 3 | a0001c0001t0028g0147 a0001c0001t0028g0148 a0001c0001t0028g0149 |
3 | HG02922.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1980-31A>C | PTCD3 | ENSG00000132300.19 | transcript | ENST00000254630.12 | protein_coding | 23/23 | chr2 | 86137438 |